AstroFlav MetaBurn PM: Boost Fat Loss While You Sleep Soundly

Since hitting the supplement scene in 2019, AstroFlav has established a reputation for being one of the most consumer-oriented brands around. They’re great at getting customer feedback and running with it.

This year, we’re finding that nobody in the industry does more than AstroFlav when it comes to continually refining and tinkering with their products. Their primary values are trust, compassion, integrity, and results.

This translates to 100% transparency with fully disclosed labels, the use of premium ingredients, and most importantly, ASTROnomically great FLAVors. In that vein, AstroFlav really lives up to their name, especially with their recent IsoMix and VeganMix releases.

AstroFlav MetaBurn PM

AstroFlav MetaBurn PM is a hybrid fat burning sleep aid that consistently focuses on brown fat activation and non-shivering thermogenesis in just a two-capsule dose!

But today, we’re talking about capsules – no flavor needed here. It turns out that they’re just as good at formulating these types of supplements, too.

Introducing AstroFlav MetaBurn: A Fat-Burning Sleep Aid

A lot of ingredients that promote sleep don’t really taste too great. When a company with a strong flavor game like AstroFlav comes to play in the sleep-aid category, we always sit up and pay attention.

Instead of trying to overwhelm a powder on the flavor front, they’re instead making a hybrid supplement that doubles as a fat-burning sleep aid: MetaBurn PM.

Nighttime: A perfect time to burn extra fat

Combining these two categories into a single product makes a ton of sense when you think about it. It’s suggested that we’re able to burn more fat at night when we’re asleep (through the breath, no less[1]), thanks to the fact that insulin levels naturally fall during sleep.[2]

The natural drop in insulin during sleep makes it a great point of leverage for amplifying fat loss – your body is primed to lose fat when asleep. After all, fat oxidation grinds to a halt when either blood glucose or insulin levels are high,[3,4] so let’s take advantage of the times when they’re destined to come down. Sleep is, after all, a forced fast of sorts.

Meanwhile, sleep is so important for fat burning and healthy-body composition that restoration of adequate sleep has been proposed as a treatment for obesity.[5] And sleep disturbances have even been shown to interfere with weight loss.[6]

With that said, let’s get ready to jump into MetaBurn PM’s mechanisms to boost sleep and fat loss even more, but first, check PricePlow for news and deals:

AstroFlav MetaBurn PM – Deals and Price Drop Alerts

Get Price Alerts

No spam, no scams.

Disclosure: PricePlow relies on pricing from stores with which we have a business relationship. We work hard to keep pricing current, but you may find a better offer.

Posts are sponsored in part by the retailers and/or brands listed on this page.

This area is reserved for Team PricePlow's upcoming videos.

Subscribe to our channel and sign up for notifications so you catch it when it goes live!

Subscribe to PricePlow on YouTube!

Ingredients

In a single 2-capsule serving of MetaBurn from AstroFlav, you get the following:

  • MitoBurn (L-β-Aminoisobutyric Acid) – 500 mg

    AstroFlav MetaBurn PM Ingredients

    As we dig into this formula, we’ll spot an incredible trend towards WAT-to-BAT conversion and non-shivering thermogenesis!

    NNB Nutrition’s MitoBurn is pure L-β-Aminoisobutyric Acid, abbreviated as L-BAIBA, which is a myokine that we call “the exercise signal”.

    Myokines are non-protein amino acids that function like hormones in your body. Hormones are messenger molecules that provide instructions to cells regarding how to function in the context of your whole body. So we sometimes refer to myokines like L-BAIBA as “muscle messengers” – they give your muscle cells information they need to regulate muscle growth and decay.

    Your body naturally produces L-BAIBA in response to exercise, which triggers the conversion of valine, an essential amino acid, into L-BAIBA.[7]

    L-BAIBA then signals to your muscle cells that exercise is underway,[8] which triggers a whole host of metabolic adaptations that help your body withstand and recover from intense exercise. These adaptations include increased fat burning, bone protection, and more.

    In other words, L-BAIBA is the molecule that actually triggers most of the body’s beneficial responses to workouts.

    Unsurprisingly, no sooner was L-BAIBA discovered than enterprising sports scientists began to wonder whether exogenous or supplemental L-BAIBA could simulate exercise, even in the absence of an actual workout. Incredibly – the answer seems to be yes.

    Taking L-BAIBA as a supplement has been shown to drive the conversion of white adipose tissue (WAT) to brown adipose tissue (BAT), a process that can increase metabolic rate by upregulating a process called non-shivering thermogenesis.[9] This takes us down the next rabbit hole:

    White adipose tissue (WAT) vs brown adipose tissue (BAT)

    To understand the significance of WAT-to-BAT conversion, we’ll talk a little bit about how the two differ.

    Together, WAT and BAT account for all the adipose tissue in your body. These two types of body fat serve very different purposes: Your body uses WAT for long-term energy story, which can be metabolized for fuel when calorie intake approaches zero.[10]

    On the other hand, BAT is not used by your body for fuel at all. It’s where non-shivering thermogenesis takes place. In non-shivering thermogenesis, your body burns cellular energy substrates (like glucose and fatty acids) for heat, which is one of the body’s primary mechanisms for maintaining body temperature in the face of cold exposure.[10]

    This ultimately contributes to your body’s total daily energy expenditure (TDEE), defined as the total number of calories your body burns in a day. A higher TDEE, thanks to non-shivering thermogenesis, translates into faster weight loss[11,12] (assuming you don’t eat more to compensate for the caloric deficit it creates).

    One of the really awesome things about BAT is that it doesn’t just burn fat for heat – it can use glucose as well, meaning that having lots of BAT can improve your blood glucose levels and lead to better metabolic health, even if you haven’t lost any body fat.[13]

    Non-shivering thermogenesis mechanism of action

    So how does non-shivering thermogenesis burn calories for heat?

    The answer is increased mitochondrial density. Compared to WAT, BAT has way more mitochondria.[14]

    MitoBurn PricePlow

    MitoBurn (L-BAIBA) has flipped the fat burner niche on its head by supplying more of this exercise-based signaling molecule to dieters

    In fact, this is where the names “white” adipose tissue and “brown” adipose tissue come from. When viewed under a microscope, white adipose tissue, being largely devoid of mitochondria, has a pale appearance because light passes through it. BAT on the other hand, being full of mitochondria compared to WAT, blocks more light and has a dark brown color.

    So the process of converting WAT to BAT entails driving the creation of new mitochondria inside existing WAT. That’s what L-BAIBA does: it drives mitochondrial biogenesis in WAT.

    These aren’t just ordinary mitochondria though. The kind of mitochondria your body grows in BAT are equipped with a protein called uncoupling protein 1 (UCP1), which short-circuits the electron transport chain. This leads the electrical potential in your mitochondria to radiate heat in exactly the same way that a short-circuited electrical circuit arcs.[15]

    The name uncoupling protein 1 refers to the fact that UCP1 decouples mitochondrial activity from the demands placed upon your body, enabling your mitochondria to burn significantly more calories without a corresponding increase in physical activity.

    Thanks to its ability to burn off excess cellular fuel, like glucose and fatty acids, UCP1 upregulation can protect against obesity[16] and increase insulin sensitivity, contributing to better overall metabolic health.

    How L-BAIBA converts WAT to BAT

    The specific mechanisms of action by which L-BAIBA turns WAT into BAT are upregulation of PGC-1 alpha and PPAR alpha.[9,17]

    L-BAIBA research

    So that’s L-BAIBA theory, but what happens in real-world studies with L-BAIBA?

    The research so far indicates that L-BAIBA can:

    BAIBA Results

    Beta-aminoisobutyric acid (BAIBA), induces beneficial effects on lipid homeostasis in mice.[18]

    • Accelerate fat burning[7,9,18-20]
    • Increase ketone production[21]
    • Convert WAT to BAT[9,20]
    • Increase insulin sensitivity and decrease blood glucose levels[7,18,22]
    • Decrease inflammation[20]
    • Improve cholesterol and triglycerides[7,18]
    • Increase bone density[23]
    • Enhance kidney function[24]

    L-BAIBA mechanism of action

    L-BAIBA works by upregulating peroxisome proliferator-activated receptor-gamma coactivator (PGC)-1alpha (PGC-1 alpha) and peroxisome proliferator-activated receptor (PPAR alpha).[25,26]

    PGC-1 alpha causes mitochondrial biogenesis.[27]

    PPAR alpha actually feeds fatty acids that constitute BAT to your mitochondria.[28]

    What’s special about MitoBurn

    Although many attempts have been made in recent years to create efficacious BAIBA supplements, getting the right form can be tricky.

    For one thing, only the L isomer of BAIBA – as opposed to D-BAIBA or R-BAIBA – has active effects on human metabolism.[7,19]

    NNB Nutrition MitoBurn

    MitoBurn from NNB Nutrition has been tested out to be a pure form of BAIBA on the market!

    This is what motivated NNB Nutrition to develop and trademark MitoBurn — a pure, standardized, and stabilized form of L-BAIBA. We wrote a long-form article on this ingredient, so if you want to learn more, mosey on over to BAIBA: Weight Loss Ingredient Generates Exercise in a Pill?!

    Now that we have some fat loss mechanisms upregulated, let’s get some relaxation and sleep started:

  • Zylaria (Xylaria nigripes, [mycelium], Cuscuta chinensis Extract [seed], Panax notoginseng Extract [root]) – 300 mg

    Xylaria nigripes (XN) is a medicinal fungus with a long history in traditional Chinese medicine (TCM), where it’s known as Wu Ling Shen. It has antioxidant,[29] anti-inflammatory,[30] and nootropic[31,32] effects, and has traditionally been used by TCM practitioners to treat a wide range of illnesses.

    Zylaria

    Zylaria is a Xylaria nigripes extract that’s shown to provide some sedative and mood-promoting benefits.

    Zylaria is a standardized extract of XN designed and trademarked by NuLiv Science. It contains the following bioactive constituents:

    • Sesquiterpenes are a type of terpenoid alkaloid that contains 15 carbon atoms and occur naturally in a huge variety of plants.[33]

      These compounds have been shown to protect the cardiovascular system by increasing the body’s production of nitric oxide (NO). But the reason we’re seeing them used in AstroFlav MetaBurn PM is they also have sedative effects.[33] For this reason, sesquiterpene-rich plants are often used as the source for calming, anxiolytic essential oils. XN has six different kinds of sesquiterpene: nigriterpenes A through F.[34]

    • Fommanoxin has significant anti-inflammatory and nootropic effects.[34]

    • Gamma-amino-butyric acid (GABA) is an anti-excitatory and inhibitory neurotransmitter that promotes rest and relaxation.[35] GABA is the antagonist of glutamate, an excitatory neurotransmitter. As it turns out, XN contains an enzyme called glutamate decarboxylase, which converts glutamate into GABA.[35]

    Xylaria nigripes’ effect on sleep

    Zylaria Relaxation

    Get relaxed with Zylaria

    According to one study published by Chinese Pharmaceutical Journal in 1991, mice who were treated with Xylaria were observed to have higher concentrations of GABA and GABA precursors in their blood, both of which go a long way toward promoting restful sleep.[36]

    One particularly interesting thing about this study is that the mice also had a higher density of GABA receptors, meaning that in addition to having more GABA, the GABA they had was more active than usual.[36]

    In 2010, the Chinese Archives of Traditional Chinese Medicine published a study that found that of a group of subjects who took a Xylaria supplement, 57.5% saw improvements in Pittsburgh Sleep Quality Index (PSQI) scores, a questionnaire designed to quantify insomnia severity.[37]

    A 2022 meta-analysis of 19 different placebo-controlled, randomized trials with a cumulative total of 1,850 participants found that Xylaria supplements consistently outperformed placebo controls when it came to improving subjects’ PSQI scores.[38] The average effect size in these studies was 2 points,[38] which is a pretty substantial difference on a 21-point scale like the PSQI.

    We can help contextualize a 2 point PSQI improvement by explaining that any score over 5 points is considered by sleep scientists to constitute a serious sleep disturbance.[39]

    While the authors of the meta-analysis caution that several of the Xylaria studies showed evidence of statistical bias,[38] there’s at least one randomized, double-blind, placebo-controlled study showing that the fungi can significantly improve sleep. Published in 2015, this was actually a study on depression that wound up discovering Xylaria’s effect on sleep quality can improve depressive symptoms.[40]

    Xylaria helps mitigate the cognitive effects of sleep deprivation

    Xylaria Benefits

    Overall quality of life improvements and more from Xylaria! Note that the Wu Ling Group is xylaria.[40]

    Insomnia is a truly crippling condition that can affect many aspects of human health and functioning. But arguably, the worst thing insomnia does is interfere with cognitive function. Fortunately for us, there’s some good evidence that Xylaria can help protect our brains against the effects of sleep deprivation.

    One 2014 study found that sleep-deprived mice who’d taken Xylaria had significantly more cyclic adenosine monophosphate (cAMP)-response element-binding protein (CREB), compared to control mice.[35]

    The reason that’s important is CREB is crucial for neuroplasticity, which is the process by which your brain physically remodels itself in response to learning. CREB is also important for long-term potentiation, the process of consolidating short-term memories into long-term ones.[35,41]

    Thus, the sleep-derived and Xylaria-treated mice did better on cognitive performance tests than sleep-deprived controls.[35]

  • Sensoril Ashwagandha (Withania somnifera) Extract (root and leaf) – 240 mg

    Ashwagandha is an evergreen shrub with a long history of use in traditional systems of folk medicine all over the world.

    Ashwagandha significantly reduces cortisol

    Ashwagandha is an adaptogenic herb that helps lower cortisol in addition to improving VO2 Max.

    It’s what we call an adaptogen, a supplement capable of normalizing various biological processes. For instance, if you have too little cortisol, an adaptogen can increase your cortisol production, whereas if you have too much cortisol, the same supplement can decrease your cortisol production.

    This paradoxical effect, tailored to each unique individual, is what makes adaptogens such a powerful tool in the supplement consumer’s arsenal.

    When it comes to ashwagandha specifically, tons of research has borne out its usefulness in managing both physical and mental stress.[42-45]

    By modulating the hypothalamic-pituitary axis (HPA),[42] the hormone synthesis pathway responsible for making stress and adrenal hormones,[42] ashwagandha can lower cortisol levels in people with elevated cortisol, and raise testosterone levels in men.[42]

    Based on these benefits, you’d probably guess that supplementing with ashwagandha leads to a lower subjective feeling of stress, which is precisely what double-blind, randomized, placebo-controlled studies have consistently found.[43-45]

    Insomnia is closely associated with HPA dysfunction and high cortisol levels.[46] So if you’re trying to sleep better, ashwagandha may help you get much closer to your goal.[46]

    Ashwagandha’s anti-obesity effects

    Besides supporting healthy body composition through improving sleep quality, ashwagandha has at least one more anti-obesity mechanism: it helps activate the browning of body fat, the same mechanism we discussed extensively in the MitoBurn section.

    Sensoril Ashwagandha

    Sensoril Ashwagandha uses both the root and the plant for a full spectrum of benefits! Image courtesy Natreon

    First, it upregulates mitochondrial function in existing BAT, helping it burn even more calories. Second, it helps fledging adipocytes (fat cells) differentiate into beige cells, which, in the long run, sets your body up for an even higher proportion of brown fat.[47]

    Sensoril ashwagandha

    Sensoril is a patented ashwagandha extract. What makes Sensoril special is that unlike competing extracts, which generally emphasize one of ashwagandha’s bioactive constituents at the expense of others, Sensoril consists of whole leaf and root extract.

    Specifically, root-only extracts tend to lack withaferin A, one of ashwagandha’s most powerful bioactives. Sensoril doesn’t suffer from this problem. It’s complete with both withaferin A and withanolides.

  • L-Theanine – 200 mg

    Theanine is an amino acid that naturally occurs in tea leaves. We should clarify that by tea we mean Camellia sinensis, the true tea plant that is the source of green tea, oolong tea, and black tea, among others.

    Theanine functions as a neurotransmitter in the brain, where it has calming, anxiolytic effects[48-51] due to its ability to inhibit neuronal activity (as opposed to exciting it, i.e. being excitatory like the neurotransmitter glutamate).

    Meta Burn PM

    Have you ever noticed that despite its caffeine content, a nice warm cup of tea can have a deeply relaxing effect? Theanine is a big part of the reason why.

    Theanine improves time to sleep onset and sleep quality

    The 200-milligram dose of theanine is standard, and its efficacy has been repeatedly attested to in research literature.[52] This is partly because theanine is GABAergic.[52,53]

    In fact, one study found that a daily 200-milligram dose of theanine taken for 4 weeks led to improved PSQI scores by about 2 points.[52] As we discussed in the Zylaria section, that’s a significant effect size.

    This study, conducted in stressed humans, found that theanine also improved verbal fluency and cognitive performance, partly because of its effects on sleep.[52]

    L-theanine can decrease time to sleep onset, helping you fall asleep faster,[54] in addition to improving sleep quality.[52,54]

    Theanine’s anti-obesity effects

    Theanine has actually been identified by at least one study as an anti-obesity constituent of green tea,[55] as it works synergistically with caffeine and catechins to suppress certain blood biomarkers that are associated with body fat accumulation.

    In fact, theanine activates the browning of body fat[56] that we discussed in the MitoBurn section.

    This is a powerful mechanism for accelerating fat loss. Anything that drives fat browning is a thumbs-up weight loss ingredient for PricePlow.

  • Rutaecarpine (100 mg)

    Now this is an interesting ingredient we want more of our readers to look into!

    Rutaecarpine (sometimes spelled rutecarpine) is an alkaloid with one particularly interesting effect: it increases your body’s rate of caffeine metabolism. Or, in other words, it decreases the half-life of caffeine in your body.[57]

    Rutaecarpine Caffeine Rats

    Possibly the most interesting chart you’ll see today. Rutaecarpine helps rats tear through caffeine![57]

    How much faster will you metabolize caffeine? One study found that rats who consumed caffeine without rutaecarpine saw peak blood-concentration levels of about 16.7 μg/mL, compared to a peak concentration of only 5.22 μg/mL in rats who got the same dose of caffeine, plus some rutaecarpine.

    Peak concentration of caffeine metabolites were roughly the same between both groups, indicating that the difference can be attributed to an increase in the rate of caffeine metabolism.[57]

    Another study in rats found that the activity of the CYP1A2 enzymes, which are created in the liver in order to metabolize caffeine, were somewhere between 3 to 7 times as active in rutaecarpine-treated rats, depending on how much time had elapsed since the rutaecarpine treatment.[58]

    This is very strong evidence that rutaecarpine can speed up the rate of caffeine detoxification in mammals. We’d love to know the pharmacokinetic effect size in humans, but as far as we’re aware, human studies have not been conducted yet.

    The CYP1A2 enzymes are responsible for removing a lot of toxic substances besides caffeine, so upregulating them can come with a number of health benefits. Among other things, high CYP1A2 activity is associated with reduced risk of breast cancer,[59] thanks to the role these enzymes play in controlling blood estrogen levels.

    In fact, rutaecarpine has a long history of use in traditional Chinese medicine (TCM) for the treatment of liver diseases.[60]

    Why caffeine elimination matters

    Caffeine’s half-life in the human body, on average, is about five hours.[61] This means that if you consume 200 milligrams of caffeine 15 hours before going to sleep (this is a pretty standard pattern of caffeine consumption) you can expect still have about 25 milligrams of caffeine in your bloodstream when you get into bed.

    Just one or two cups of coffee is enough to get you 200 milligrams of caffeine, and 25 milligrams is about what you’d expect to find in a cup of green tea. So essentially, even if you stop drinking caffeinated beverages early in the morning, the amount of caffeine in your system at bedtime could be about the same as the amount you’d get from drinking a cup of green tea immediately before bed.

    AstroFlav MetaBurn PM

    Now, individual caffeine tolerances vary, but it’s safe to say that many individuals will struggle to achieve restful sleep under these circumstances. This isn’t even considering the fact that many American adults consume significantly more than one or two cups of coffee’s worth of caffeine in a day, and generally do not cease to consume caffeine until the afternoon, or even later.

    If you’re after more restful sleep but don’t want to reduce or eliminate your caffeine intake, rutaecarpine can definitely help move the needle in the direction you want. It can help eliminate caffeine from your system significantly faster than you’d be able to naturally.

    Rutaecarpine’s anti-obesity effects

    Once again, consistent with the pattern of ingredient choice in MetaBurn PM, we see that besides potentially improving sleep quality in caffeine users (most of us), rutaecarpine can have direct anti-obesity effects.

    Rutaecarpine has been shown to increase fat browning and drive non-shivering thermogenesis in BAT by activating the energy metabolic pathway, AMP-activated protein kinase (AMPK)/PGC-1α axis.[62]

    Rutaecarpine’s safety profile

    For some reason, there’s occasionally an argument in supplement circles that rutaecarpine can cause liver injury. However, we’re not aware of any rigorous evidence showing this to be the case. On the contrary, CYP1A2 upregulation constitutes an improvement in liver function.

    In fact, a mouse study found that rutaecarpine actually protected the mice’s livers from acetaminophen-induced damage.[25]

    A safety study found that the median lethal dose of rutaecarpine in mice is about 65 milligrams per kilogram of bodyweight, the human equivalent of which is about 11 milligrams per kilogram.[63]

    Another safety study found that rutaecarpine protected mouse livers against damage from tert-butyl hydroperoxide (t-BHP), another known liver toxin.[64]

    Again, we haven’t seen safety studies conducted in humans, so it’s impossible to say definitively that rutaecarpine is safe for human consumption. But so far, all the actual evidence points the other way: rutaecarpine appears to potentially improve liver health and function. Additionally, note that the dosage here is nowhere near what is tested in the studies cited above.

    As always, if you aren’t sure whether you can take rutaecarpine, ask your doctor before doing so.

  • Apigenin – 50 mg

    Apigenin is a flavonoid that’s known for activating benzodiazepine receptors[65] which can produce a state of relaxation and reduce anxiety. In fact, apigenin has been proposed as the molecule behind the sedative effects of chamomile,[66,67] a well-known over-the-counter sleep aid that we’ve written about multiple times on the PricePlow Blog.

    AstroFlav IsoMix

    AstroFlav IsoMix – a delicious pure whey protein isolate with “Out of This World Flavor” – is back with six flavors, boosted by MCT and inulin.

    Chamomile extracts are sometimes standardized for apigenin, but AstroFlav decided to cut out the middleman and go straight for pure apigenin. We think this is a good idea – chamomile is about 1% apigenin by weight, so to get a 50-milligram dose of apigenin from chamomile, you’d need about 6 grams of chamomile.[67] That’s a big enough dose to mostly fill ten veggie caps on its own, which isn’t practical for inclusion in a multi-ingredient sleep supplement.

    Of course, promoting sleep is only half of the MetaBurn PM value proposition: we also want to torch fat and improve metabolic health, which apigenin can help with as well.

    Apigenin is an aromatase inhibitor and reduces estrogen levels

    It’s somewhat common knowledge that being overweight can increase aromatase activity,[28] an enzyme that converts androgens (like testosterone) into estradiol (a strong form of estrogen).[68]

    What’s discussed a lot less is that the causal relationship is bi-directional: having elevated estrogen levels can also contribute to unwanted weight gain.[26,27] The estrogen hypothesis of obesity proposes that increased estrogen levels may even be the primary cause of obesity.[27]

    With that in mind, it’s good to know that apigenin is a strong natural aromatase inhibitor.[69]

    Aromatase inhibiting supplements are particularly useful in 21st-century America, as estrogen dominance is a growing concern for supplement consumers. Unfortunately, our environment is increasingly populated by synthetic xenoestrogen compounds, which mimic the action of natural estrogens by activating estrogen receptors, thus contributing to your body’s overall estrogen burden.[70]

    Of course, apigenin’s aromatase-inhibiting effects can’t compete with those of pharmaceutical aromatase inhibitors, but a little extra inhibition of aromatase usually can’t hurt (it’s possible, though unlikely, to have too little estrogen. So talk to your doctor if you aren’t sure where you fall on the estrogen spectrum).

    Apigenin drives fat browning

    We’re not done yet. Once again, we have yet another ingredient that can contribute to WAT to BAT conversion. Apigenin has been shown to induce the browning of white fat cells through VEGF-PRDM16 signaling.[71]

  • BioPerine – 15 mg

    BioPerine is an extract from black pepper that works to enhance the bioavailability of whatever it’s stacked with. Put another way, BioPerine makes every other ingredient in MetaBurn PM more effective than normal. And here, we have three times the usual dose!

    The molecule responsible for BioPerine’s bioavailability enhancement is piperine,[72] a powerful antioxidant[73] that inhibits stomach enzymes, which ordinarily break down ingredients before they can be absorbed through the intestinal wall.

    Piperine’s anti-obesity effects

    AstroFlav MetaBurn PM

    Piperine also upregulates a protein called glucose transporter 4 (GLUT4), which promotes glucose uptake by your muscle cells. This naturally helps keep blood glucose under control and, as a result, usually improves overall metabolic health. In fact, in mice, GLUT4 overexpression has been shown to reverse insulin resistance and diabetes.[74]

    Piperine can also increase insulin sensitivity while removing adipose tissue from the liver.[75] This is a big deal because the untoward accumulation of fat in the liver – known as non-alcoholic fatty liver disease (NAFLD) – is associated with metabolic dysfunction, a condition that can culminate with diabetes and obesity.[76]

    Defatting the liver is a potentially powerful way to improve metabolic function in people whose metabolic health has already been compromised. And even if you don’t have fatty liver, taking supplements like BioPerine can be a great preventative measure against NAFLD.

    Piperine and non-shivering thermogenesis

    Yet again, we see an ingredient in MetaBurn PM that prioritizes non-shivering thermogenesis in BAT – piperine has been shown to upregulate UCP1 and increase the amount of energy your body expends in thermogenesis.[77]

  • Melatonin (as MicroActive) – 2 mg

    Melatonin is a hormone responsible for regulating your circadian rhythm, which signals to your body that it’s time for sleep.[78] Although the body synthesizes some melatonin on its own, research shows that supplemental melatonin can improve sleep onset and quality.

    How melatonin secretion interacts with blue light

    One of melatonin’s functions is to synchronize circadian rhythms – to set your body’s internal clock for waking and sleeping.[79] Here’s how it works: melatonin is produced by an enzyme called arylalkylamine N-acetyltransferase that’s suppressed when we’re exposed to a lot of light (i.e., when the sun comes up,[80] which wakes us up in part by suppressing melatonin production).[81]

    Melatonin Benefits

    Melatonin supplementation improves QOS (quality of sleep) and has a relatively high response rate, even at low doses.

    The component of sunlight that suppresses melatonin most prominently is the blue light,[82] which makes intuitive sense since the color blue usually dominates our perception of the daytime sky.

    Unfortunately, other sources of blue light, such as television screens, computer monitors, and cell phones, can also suppress arylalkylamine N-acetyltransferase.[83] So our gadgets can suppress melatonin production exactly the same way that sunlight does!

    Thanks to artificial light and the increasing role that technology plays in daily life, we’re all being exposed to unprecedented amounts of artificial blue light, especially in the evening hours when our natural circadian clock is supposed to be winding us down for sleep.

    Melatonin supplements, when taken at the right time (i.e., shortly before bed), can help correct this problem. They often improve sleep quality without significant adverse effects, particularly in adults 55 years of age and older.[84]

    Other studies have found that supplemental melatonin can even correct severe sleep disturbances.[85,86]

    We recommend taking melatonin supplements only at the appropriate time, which is shortly before bed, and combining them with good sleep hygiene practices like limiting your exposure to blue light in the evening.[87]

    Melatonin’s anti-obesity effects

    Again, like most of the other ingredients in AstroFlav MetaBurn, melatonin has been shown to increase brown fat non-shivering thermogenesis by increasing the expression of UCP1.[88] Spotting a trend in MetaBurn PM?!

No flavor? No problem. AstroFlav Continues to Impress

AstroFlav Full Tank Intra-Workout

Make your last sets as strong as your first with AstroFlav’s Full Tank Intra-Workout Supplement.

The best supplements are organized around a coherent idea, and AstroFlav’s MetaBurn PM is a prime example of how this approach can be successful.

Almost all of the ingredients in this product improve sleep quality and accelerate fat burning. And what’s even better is that almost all of the fat-burning ingredients act on the same mechanism, which is the upregulation of non-shivering thermogenesis, either by increasing mitochondrial activity in existing brown fat or driving the conversion of white fat to brown fat.

It’s clear that AstroFlav put a lot of thought into their ingredient selection. We expect MetaBurn to not only improve the quality of your sleep, but also send your brown-fat activity levels into the stratosphere through the additive effects of multiple ingredients that act on brown fat by complementary mechanisms.

AstroFlav MetaBurn PM Label

AstroFlav MetaBurn PM – Deals and Price Drop Alerts

Get Price Alerts

No spam, no scams.

Disclosure: PricePlow relies on pricing from stores with which we have a business relationship. We work hard to keep pricing current, but you may find a better offer.

Posts are sponsored in part by the retailers and/or brands listed on this page.

About the Author: Mike Roberto

Mike Roberto

Mike Roberto is a research scientist and water sports athlete who founded PricePlow. He is an n=1 diet experimenter with extensive experience in supplementation and dietary modification, whose personal expertise stems from several experiments done on himself while sharing lab tests.

Mike's goal is to bridge the gap between nutritional research scientists and non-academics who seek to better their health in a system that has catastrophically failed the public.

No Comments | Posted in | Tagged , , , , , , , , , , , , , , , , , , , , , .

References

  1. Meerman, R., and A. J. Brown. “When Somebody Loses Weight, Where Does the Fat Go?” BMJ, vol. 349, no. dec16 13, 16 Dec. 2014, pp. g7257–g7257, 10.1136/bmj.g7257; https://www.bmj.com/content/349/bmj.g7257
  2. Van Cauter, E et al. “Modulation of glucose regulation and insulin secretion by circadian rhythmicity and sleep.” The Journal of clinical investigation vol. 88,3 (1991): 934-42. doi:10.1172/JCI115396; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC295490/
  3. Sidossis, L, et al; “Glucose and insulin-induced inhibition of fatty acid oxidation: the glucose-fatty acid cycle reversed”; American Journal of Physiology; 270(4 Pt 1):E733-8; April 1996; https://pubmed.ncbi.nlm.nih.gov/8928782
  4. Bonadonna, R; “Dose-dependent effect of insulin on plasma free fatty acid turnover and oxidation in humans”; The American Journal of Physiology; 259(5 Pt 1):E736-50; November 1990; https://pubmed.ncbi.nlm.nih.gov/2240211
  5. Chaput, Jean-Philippe, and Angelo Tremblay. “Adequate sleep to improve the treatment of obesity.” CMAJ : Canadian Medical Association journal = journal de l’Association medicale canadienne vol. 184,18 (2012): 1975-6. doi:10.1503/cmaj.120876 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3519150/
  6. Nedeltcheva, Arlet V et al. “Insufficient sleep undermines dietary efforts to reduce adiposity.” Annals of internal medicine vol. 153,7 (2010): 435-41. doi:10.7326/0003-4819-153-7-201010050-00006 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2951287/
  7. Tanianskii, Dmitrii A et al; “Beta-Aminoisobutyric Acid as a Novel Regulator of Carbohydrate and Lipid Metabolism”; Nutrients; vol. 11,3 524; February 28, 2019; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6470580/
  8. Schnyder, Svenia, Handschin, Christoph; “Skeletal muscle as an endocrine organ: PGC-1α, myokines and exercise”; Bone; Volume 80, Pages 115-125; November 2015; https://www.sciencedirect.com/science/article/abs/pii/S8756328215000459
  9. Roberts, L, et al; “b-Aminoisobutyric Acid Induces Browning of White Fat and Hepatic b-Oxidation and Is Inversely Correlated with Cardiometabolic Risk Factors”; Cell Metabolism; Volume 19, Issue 1, pp 96-108; 2014; https://www.cell.com/cell-metabolism/fulltext/S1550-4131(13)00497-X
  10. Rosenwald M, Wolfrum C; “The origin and definition of brite versus white and classical brown adipocytes”; Adipocyte; 2014;3(1):4-9; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3917931/
  11. Sugita, J., Yoneshiro, T., et al; “Grains of paradise (Aframomum melegueta) extract activates brown adipose tissue and increases whole-body energy expenditure in men”; British Journal of Nutrition; (2013) 110(4), pp. 733–738; https://www.cambridge.org/core/journals/british-journal-of-nutrition/article/grains-of-paradise-aframomum-melegueta-extract-activates-brown-adipose-tissue-and-increases-whole-body-energy-expenditure-in-men/517F8F0D73864C919E42D502537BA01D/core-reader
  12. Sugita J, Yoneshiro T, et al; “Daily ingestion of grains of paradise (Aframomum melegueta) extract increases whole-body energy expenditure and decreases visceral fat in humans”; Journal of Nutritional Science and Vitaminology; 2014, 60(1): 22-27; https://www.jstage.jst.go.jp/article/jnsv/60/1/60_22/_pdf
  13. Kim SH, Plutzky J; “Brown Fat and Browning for the Treatment of Obesity and Related Metabolic Disorders”; Diabetes & Metabolism Journal. 2016;40(1):12-21; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4768046/
  14. “Brown Adipose Tissue – an Overview | ScienceDirect Topics.”; ScienceDirect; https://www.sciencedirect.com/topics/medicine-and-dentistry/brown-adipose-tissue
  15. Porter, Craig. “Quantification of UCP1 function in human brown adipose tissue.” Adipocyte vol. 6,2 (2017): 167-174. doi:10.1080/21623945.2017.1319535 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5477712/
  16. ‌Kozak, L P, and R Anunciado-Koza. “UCP1: its involvement and utility in obesity.” International journal of obesity (2005) vol. 32 Suppl 7,Suppl 7 (2008): S32-8. doi:10.1038/ijo.2008.236; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2746324/
  17. Bostrom, P., et al. (2012). A PGC1-a-dependent myokine that drives brown-fat-like development of white fat and thermogenesis. Nature, 481: 463-482; https://www.ncbi.nlm.nih.gov/pubmed/22237023
  18. Begriche, Karima, et al. “β-Aminoisobutyric Acid Prevents Diet-Induced Obesity in Mice with Partial Leptin Deficiency.” Obesity, vol. 16, no. 9, Sept. 2008, pp. 2053–2067, 10.1038/oby.2008.337; https://onlinelibrary.wiley.com/doi/full/10.1038/oby.2008.337
  19. Maisonneuve, C, et al; “Effects of zidovudine, stavudine and beta-aminoisobutyric acid on lipid homeostasis in mice: possible role in human fat wasting”; Antiviral Therapy; 9(5):801-10; October 2004; https://pdfs.semanticscholar.org/ad85/0e69e7a66f59bd0491fbf2b39da15f6eb2cf.pdf
  20. Jung, Tae Woo, et al; “BAIBA attenuates insulin resistance and inflammation induced by palmitate or a high fat diet via an AMPK–PPARδ-dependent pathway in mice”; Diabetologia; September 2015, Volume 58, Issue 9, pp 2096–2105; https://link.springer.com/article/10.1007/s00125-015-3663-z
  21. Note, Reine et al; “Mitochondrial and metabolic effects of nucleoside reverse transcriptase inhibitors (NRTIs) in mice receiving one of five single- and three dual-NRTI treatments”; Antimicrobial agents and Chemotherapy; vol. 47,11: 3384-92; 2013; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC253807/
  22. Kammoun, HL and Febbraio, MA; “Come on BAIBA Light My Fire;” Cell Metabolism; 2014;19(1), pp 1-2; https://www.sciencedirect.com/science/article/pii/S1550413113005020
  23. Kitase, Yukiko et al; “β-aminoisobutyric Acid, l-BAIBA, Is a Muscle-Derived Osteocyte Survival Factor”; Cell Reports; vol. 22,6 (2018): 1531-1544; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5832359/
  24. Wang, H, et al; “β-Aminoisobutyric acid ameliorates the renal fibrosis in mouse obstructed kidneys via inhibition of renal fibroblast activation and fibrosis”; Journal of Pharmacological Sciences; Volume 133, Issue 4; Pages 203-213; April 2017; https://www.sciencedirect.com/science/article/pii/S1347861317300038
  25. Choi, Jae Ho et al. “Rutaecarpine Protects against Acetaminophen-Induced Acute Liver Injury in Mice by Activating Antioxidant Enzymes.” Antioxidants (Basel, Switzerland) vol. 10,1 86. 10 Jan. 2021, doi:10.3390/antiox10010086 ; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7827407/
  26. Brigitte Leeners, Nori Geary, Philippe N. Tobler, Lori Asarian, Ovarian hormones and obesity, Human Reproduction Update, Volume 23, Issue 3, May-June 2017, Pages 300–321; https://academic.oup.com/humupd/article/23/3/300/3058798
  27. ‌Grantham, James P., and Maciej Henneberg. “The Estrogen Hypothesis of Obesity.” PLoS ONE, vol. 9, no. 6, 10 June 2014; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4051760/
  28. Mair, Kirsty M et al. “Obesity, estrogens and adipose tissue dysfunction – implications for pulmonary arterial hypertension.” Pulmonary circulation vol. 10,3 2045894020952019. 18 Sep. 2020, doi:10.1177/2045894020952023; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7506791/
  29. Ko, Huey-Jiun, et al. “Antioxidant and Antiradical Activities of Wu Ling Shen in a Cell Free System.” The American Journal of Chinese Medicine, vol. 37, no. 04, Jan. 2009, pp. 815–828, 10.1142/s0192415x09007260; https://pubmed.ncbi.nlm.nih.gov/19655417/
  30. Ko, Huey-Jiun, et al. “Immunomodulatory Properties of Xylaria Nigripes in Peritoneal Macrophage Cells of Balb/c Mice.” Journal of Ethnopharmacology, vol. 138, no. 3, 8 Dec. 2011, pp. 762–768, 10.1016/j.jep.2011.10.022; https://pubmed.ncbi.nlm.nih.gov/22044578/
  31. Zhao, Zhengqing, et al. “Xylaria Nigripes Mitigates Spatial Memory Impairment Induced by Rapid Eye Movement Sleep Deprivation.” International Journal of Clinical and Experimental Medicine, vol. 7, no. 2, 15 Feb. 2014, pp. 356–362. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3931588/
  32. Li, DQ. “Wuling Capsule Promotes Hippocampal Neurogenesis by Improving Expression of Connexin 43 in Rats Exposed to Chronic Unpredictable Mild Stress.” Journal of Chinese Integrative Medicine, vol. 8, no. 7, 15 July 2010, pp. 662–669, 10.3736/jcim20100710; https://pubmed.ncbi.nlm.nih.gov/20619143/
  33. Chadwick, Martin, et al. “Sesquiterpenoids Lactones: Benefits to Plants and People.” International Journal of Molecular Sciences, vol. 14, no. 6, 19 June 2013, pp. 12780–12805, 10.3390/ijms140612780; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3709812/
  34. Chang, Jung-Chun, et al. “Bioactive Constituents from the Termite Nest-Derived Medicinal Fungus Xylaria Nigripes.” Journal of Natural Products, vol. 80, no. 1, 27 Jan. 2017, pp. 38–44, 10.1021/acs.jnatprod.6b00249; https://pubmed.ncbi.nlm.nih.gov/28055210/
  35. Zhao, Zhengqing, et al. “Xylaria Nigripes Mitigates Spatial Memory Impairment Induced by Rapid Eye Movement Sleep Deprivation.” International Journal of Clinical and Experimental Medicine, vol. 7, no. 2, 15 Feb. 2014, pp. 356–362; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3931588/
  36. Ma, Zhizhang, et al. “Studies on the sedative and sleeping effects of Wuling mycelia and its pharmacological mechanism.” Chinese Pharmaceutical Journal, vol. 34, 1999, pp. 374–77; https://en.cnki.com.cn/Article_en/CJFDTotal-ZGYX906.006.htm
  37. Song, Xiu-Hua, et al. “Research on treatment effects of Wuling capsule for sub-healthy state insomnia.” Chinese Archives of Traditional Chinese Medicine, vol. 28, 2010, pp. 477–78; https://en.cnki.com.cn/Article_en/CJFDTotal-ZYHS201003015.htm
  38. Zhou H, Zhao Y, Peng W, Han W, Wang D, Wang Z, Ren X, Pan G, Lin Q, Wang X. Efficacy and safety of Wuling capsule for insomnia disorder: a systematic review and meta-analysis of randomized controlled trials. Sleep Med. 2022 May;93:1-14. doi: 10.1016/j.sleep.2022.03.014; https://www.sciencedirect.com/science/article/pii/S1389945722000909
  39. “Pittsburgh Sleep Quality Index – an Overview | ScienceDirect Topics.” Science Direct; https://www.sciencedirect.com/topics/medicine-and-dentistry/pittsburgh-sleep-quality-index
  40. Peng, Wei-Feng, et al. “The Anti-Depression Effect of Xylaria Nigripes in Patients with Epilepsy: A Multicenter Randomized Double-Blind Study.” Seizure – European Journal of Epilepsy, vol. 29, 1 July 2015, pp. 26–33, 10.1016/j.seizure.2015.03.014. https://www.seizure-journal.com/article/S1059-1311(15)00084-9/fulltext
  41. Kaleem, Afshan et al. “CREB in long-term potentiation in hippocampus: role of post-translational modifications-studies In silico.” Journal of cellular biochemistry vol. 112,1 (2011): 138-46. doi:10.1002/jcb.22909 https://onlinelibrary.wiley.com/doi/10.1002/jcb.22909
  42. Lopresti, Adrian L et al. “An investigation into the stress-relieving and pharmacological actions of an ashwagandha (Withania somnifera) extract: A randomized, double-blind, placebo-controlled study.”; Medicine vol. 98,37 (2019): e17186; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6750292/
  43. Chandrasekhar, K et al. “A prospective, randomized double-blind, placebo-controlled study of safety and efficacy of a high-concentration full-spectrum extract of ashwagandha root in reducing stress and anxiety in adults.” Indian journal of psychological medicine vol. 34,3 (2012): 255-62; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3573577/
  44. Andrade C, Aswath A, Chaturvedi SK, et al. “A double-blind, placebo-controlled evaluation of the anxiolytic efficacy of an ethanolic extract of withania somnifera”; Indian J Psychiatry 2000;42:295–301; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2958355/
  45. Auddy B, Hazra J, Mitra A, et al. A standardized Withania Somnifera extract significantly reduces stress-related parameters in chronically stressed humans: a double-blind, randomized, placebo-controlled study. J Am Nutraceut Assoc 2008;11:50–6; https://www.semanticscholar.org/paper/A-Standardized-Withania-Somnifera-Extract-Reduces-A-Auddy-Hazra/46bdaebfcf4f00730ad217fd6bb88228964e4c2e
  46. Dressle, Raphael J et al. “HPA axis activity in patients with chronic insomnia: A systematic review and meta-analysis of case-control studies.” Sleep medicine reviews vol. 62 (2022): 101588. doi:10.1016/j.smrv.2022.101588; https://www.sciencedirect.com/science/article/abs/pii/S1087079222000016?via%3Dihub
  47. Lee, Da-Hye et al. “Withania somnifera Extract Enhances Energy Expenditure via Improving Mitochondrial Function in Adipose Tissue and Skeletal Muscle.” Nutrients vol. 12,2 431. 7 Feb. 2020, doi:10.3390/nu12020431 https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/32046183/
  48. Juneja, L. R., et al; “L-Theanine-a Unique Amino Acid of Green Tea and Its Relaxation Effect in Humans.;” Trends in Food Science & Technology; Elsevier; 17 Dec. 1999; https://www.sciencedirect.com/science/article/abs/pii/S0924224499000448
  49. Lu, Kristy, et al; “The Acute Effects OfL-Theanine in Comparison with Alprazolam on Anticipatory Anxiety in Humans.”; Human Psychopharmacology: Clinical and Experimental; vol. 19; no. 7; 2004; pp. 457–465; https://espace.library.uq.edu.au/view/UQ:284103
  50. Haskell, C F, et al; “The Effects of L-Theanine, Caffeine and Their Combination on Cognition and Mood.”; Current Neurology and Neuroscience Reports; U.S. National Library of Medicine; Feb. 2008; https://www.ncbi.nlm.nih.gov/pubmed/18006208
  51. Lu, K; The acute effects of L-theanine in comparison with alprazolam on anticipatory anxiety in humans; Human Psychopharmacology, 19 7: 457-465; 2004; http://espace.library.uq.edu.au/view/UQ:284103
  52. Hidese, Shinsuke et al. “Effects of L-Theanine Administration on Stress-Related Symptoms and Cognitive Functions in Healthy Adults: A Randomized Controlled Trial.” Nutrients vol. 11,10 2362. 3 Oct. 2019, doi:10.3390/nu11102362; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6836118/
  53. Haskell, C F, et al; “The Effects of L-Theanine, Caffeine and Their Combination on Cognition and Mood.”; Current Neurology and Neuroscience Reports; U.S. National Library of Medicine; Feb. 2008; https://www.ncbi.nlm.nih.gov/pubmed/18006208
  54. Kim, Suhyeon et al. “GABA and l-theanine mixture decreases sleep latency and improves NREM sleep.” Pharmaceutical biology vol. 57,1 (2019): 65-73. doi:10.1080/13880209.2018.1557698; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6366437/
  55. Zheng, Guodong et al. “Anti-obesity effects of three major components of green tea, catechins, caffeine and theanine, in mice.” In vivo (Athens, Greece) vol. 18,1 (2004): 55-62. http://iv.iiarjournals.org/cgi/pmidlookup?view=long&pmid=15011752
  56. Peng, Wan-Qiu et al. “l-Theanine Activates the Browning of White Adipose Tissue Through the AMPK/α-Ketoglutarate/Prdm16 Axis and Ameliorates Diet-Induced Obesity in Mice.” Diabetes vol. 70,7 (2021): 1458-1472. doi:10.2337/db20-1210 https://diabetesjournals.org/diabetes/article-lookup/doi/10.2337/db20-1210
  57. Noh K, et al; “Effects of rutaecarpine on the metabolism and urinary excretion of caffeine in rats”; Arch Pharm Res. (2011); https://www.ncbi.nlm.nih.gov/pubmed/21468923
  58. Estari, Rohit Kumar et al. “Time effect of rutaecarpine on caffeine pharmacokinetics in rats.” Biochemistry and biophysics reports vol. 28 101121. 6 Sep. 2021, doi:10.1016/j.bbrep.2021.101121; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8429912/
  59. Hong, Chi-Chen et al. “Cytochrome P450 1A2 (CYP1A2) activity and risk factors for breast cancer: a cross-sectional study.” Breast cancer research : BCR vol. 6,4 (2004): R352-65. doi:10.1186/bcr798; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC468638/
  60. Li, Xiaojiaoyang et al. “Evodiamine and rutaecarpine from Tetradium ruticarpum in the treatment of liver diseases.” Phytomedicine : international journal of phytotherapy and phytopharmacology vol. 68 (2020): 153180. doi:10.1016/j.phymed.2020.153180 https://linkinghub.elsevier.com/retrieve/pii/S0944-7113(20)30013-1
  61. US), Medicine. “Pharmacology of Caffeine.” Nih.gov, National Academies Press (US), 2014; https://www.ncbi.nlm.nih.gov/books/NBK223808/
  62. Chen, Dandan et al. “Rutaecarpine Promotes Adipose Thermogenesis and Protects against HFD-Induced Obesity via AMPK/PGC-1α Pathway.” Pharmaceuticals (Basel, Switzerland) vol. 15,4 469. 13 Apr. 2022, doi:10.3390/ph15040469 https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/35455466/
  63. Yang, X-W et al. “Studies on the alkaloid constituents of Evodia rutaecarpa (Juss) Benth var. bodinaieri (Dode) Huang and their acute toxicity in mice.” Journal of Asian natural products research vol. 8,8 (2006): 697-703. doi:10.1080/10286020412331286425; https://pubmed.ncbi.nlm.nih.gov/17145657/
  64. Jin, Sun Woo et al. “Protective effect of rutaecarpine against t-BHP-induced hepatotoxicity by upregulating antioxidant enzymes via the CaMKII-Akt and Nrf2/ARE pathways.” Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association vol. 100 (2017): 138-148. doi:10.1016/j.fct.2016.12.031; https://linkinghub.elsevier.com/retrieve/pii/S0278-6915(16)30492-6
  65. Viola, H et al. “Apigenin, a component of Matricaria recutita flowers, is a central benzodiazepine receptors-ligand with anxiolytic effects.” Planta medica vol. 61,3 (1995): 213-6. doi:10.1055/s-2006-958058; https://www.thieme-connect.com/products/ejournals/abstract/10.1055/s-2006-958058
  66. Srivastava, Janmejai K et al. “Chamomile: A herbal medicine of the past with bright future.” Molecular medicine reports vol. 3,6 (2010): 895-901. doi:10.3892/mmr.2010.377; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2995283/
  67. “Chamomile – an Overview | ScienceDirect Topics.” ScienceDirect; https://www.sciencedirect.com/topics/agricultural-and-biological-sciences/chamomile
  68. ‌Shay DA, Vieira-Potter VJ and Rosenfeld CS (2018) Sexually Dimorphic Effects of Aromatase on Neurobehavioral Responses. Front. Mol. Neurosci. 11:374. doi: 10.3389/fnmol.2018.00374; https://www.frontiersin.org/articles/10.3389/fnmol.2018.00374/full
  69. Balunas, Marcy J et al. “Natural products as aromatase inhibitors.” Anti-cancer agents in medicinal chemistry vol. 8,6 (2008): 646-82; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3074486/
  70. Reddy, Varun et al. “Xenoestrogens impact brain estrogen receptor signaling during the female lifespan: A precursor to neurological disease?.” Neurobiology of disease vol. 163 (2022): 105596. doi:10.1016/j.nbd.2021.105596; https://linkinghub.elsevier.com/retrieve/pii/S0969-9961(21)00345-4
  71. Sreeku, Sreelekshmi, et al. Apigenin Induces Browning in White Adipocytes Mediated by VEGF-PRDM16 Signaling. 7 Jan. 2022; https://www.researchgate.net/publication/357664159_Apigenin_Induces_Browning_in_White_Adipocytes_Mediated_by_VEGF-PRDM16_Signaling
  72. Kesarwani, Kritika et al. “Bioavailability enhancers of herbal origin: an overview.” Asian Pacific journal of tropical biomedicine vol. 3,4 (2013): 253-66. doi:10.1016/S2221-1691(13)60060-X; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3634921/
  73. Mittal R, Gupta RL. In vitro antioxidant activity of piperine. Methods Find Exp Clin Pharmacol. 2000 Jun;22(5):271-4. doi: 10.1358/mf.2000.22.5.796644; https://pubmed.ncbi.nlm.nih.gov/11031726/
  74. Carvalho, Eugenia, et al. “Adipose-Specific Overexpression of GLUT4 Reverses Insulin Resistance and Diabetes in Mice Lacking GLUT4 Selectively in Muscle.” American Journal of Physiology-Endocrinology and Metabolism, vol. 289, no. 4, Oct. 2005, pp. E551–E561, 10.1152/ajpendo.00116.2005; https://journals.physiology.org/doi/full/10.1152/ajpendo.00116.2005
  75. Choi S, Choi Y, Choi Y, Kim S, Jang J, Park T. Piperine reverses high fat diet-induced hepatic steatosis and insulin resistance in mice. Food Chem. 2013 Dec 15;141(4):3627-35. doi: 10.1016/j.foodchem.2013.06.028; https://pubmed.ncbi.nlm.nih.gov/23993530/
  76. Targher, Giovanni, et al. “The Complex Link between NAFLD and Type 2 Diabetes Mellitus — Mechanisms and Treatments.” Nature Reviews Gastroenterology & Hepatology, vol. 18, no. 9, 1 Sept. 2021, pp. 599–612; 10.1038/s41575-021-00448-y; https://www.nature.com/articles/s41575-021-00448-y
  77. ‌Kim, Nami, et al. “Piperine Regulates UCP1 through the AMPK Pathway by Generating Intracellular Lactate Production in Muscle Cells.” Scientific Reports, vol. 7, no. 1, 24 Jan. 2017, 10.1038/srep41066; https://www.nature.com/articles/srep41066
  78. Tordjman, Sylvie et al. “Melatonin: Pharmacology, Functions and Therapeutic Benefits.” Current neuropharmacology vol. 15,3 (2017): 434-443. doi:10.2174/1570159X14666161228122115 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5405617/
  79. Xie, Zizhen et al. “A review of sleep disorders and melatonin.” Neurological research vol. 39,6 (2017): 559-565. doi:10.1080/01616412.2017.1315864 https://pubmed.ncbi.nlm.nih.gov/28460563/
  80. Hardeland, R. “Melatonin, hormone of darkness and more: occurrence, control mechanisms, actions and bioactive metabolites.” Cellular and molecular life sciences : CMLS vol. 65,13 (2008): 2001-18. doi:10.1007/s00018-008-8001-x. https://pubmed.ncbi.nlm.nih.gov/18344019/
  81. Gooley, Joshua J et al. “Exposure to room light before bedtime suppresses melatonin onset and shortens melatonin duration in humans.” The Journal of clinical endocrinology and metabolism vol. 96,3 (2011): E463-72. doi:10.1210/jc.2010-2098. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3047226/
  82. Tähkämö, Leena et al. “Systematic review of light exposure impact on human circadian rhythm.” Chronobiology international vol. 36,2 (2019): 151-170. doi:10.1080/07420528.2018.1527773 https://www.tandfonline.com/doi/full/10.1080/07420528.2018.1527773
  83. Tähkämö, Leena et al. “Systematic review of light exposure impact on human circadian rhythm.” Chronobiology international vol. 36,2 (2019): 151-170. doi:10.1080/07420528.2018.1527773. https://pubmed.ncbi.nlm.nih.gov/30311830/
  84. Lemoine, Patrick, et al. “Prolonged-release melatonin improves sleep quality and morning alertness in insomnia patients aged 55 years and older and has no withdrawal effects.” Journal of Sleep Research vol 16,4 (2007): 372-80. doi:10.111/j.1365-2869.2007.00613.x https://onlinelibrary.wiley.com/doi/full/10.1111/j.1365-2869.2007.00613.x
  85. Alstadhaug, K. B., et al. “Prophylaxis of Migraine with Melatonin: A Randomized Controlled Trial.” Neurology, vol. 75, no. 17, 25 Oct. 2010, pp. 1527–1532, 10.1212/wnl.0b013e3181f9618c; https://pubmed.ncbi.nlm.nih.gov/20975054/
  86. Luthringer, Remy, et al. “The Effect of Prolonged-Release Melatonin on Sleep Measures and Psychomotor Performance in Elderly Patients with Insomnia.” International Clinical Psychopharmacology, vol. 24, no. 5, Sept. 2009, pp. 239–249, 10.1097/yic.0b013e32832e9b08; https://pubmed.ncbi.nlm.nih.gov/19584739/
  87. van Geijlswijk, Ingeborg M et al. “Evaluation of sleep, puberty and mental health in children with long-term melatonin treatment for chronic idiopathic childhood sleep onset insomnia.” Psychopharmacology vol. 216,1 (2011): 111-20. doi:10.1007/s00213-011-2202-y; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3111733/
  88. Guan, Qingyun et al. “Mechanisms of Melatonin in Obesity: A Review.” International journal of molecular sciences vol. 23,1 218. 25 Dec. 2021, doi:10.3390/ijms23010218 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8745381/

Comments and Discussion (Powered by the PricePlow Forum)