HO
Hoodia Gord.

Hoodia Gordonii

herb· General
D-Tier · Preliminary28 citations
Found in 1 products
Quick Answer:The clinical dose of Hoodia Gordonii is 1000mg (Extract). Hoodia gordonii contains a steroidal glycoside known as P57, which was theorized to act on the hypothalamus similarly to glucose to signal fullness and suppress appetite.Found in 1 products on SuppVault.
// Ask SuppVault anything...
what dose do I need?which pre-workout has the most?safe with my meds?
Products Containing Hoodia Gordonii
1 products contain Hoodia Gordonii.
Shop All 1 Products with Hoodia Gordonii →
Mechanism of Action

The Biochemistry of P57 and Hypothalamic Satiety Signaling

The primary bioactive compound in Hoodia gordonii is an oxypregnane steroidal glycoside known as P57 (specifically, P57AS3). The theoretical mechanism of action for P57 centers on its ability to influence the central nervous system, specifically the hypothalamus, which is the brain's primary control center for hunger and satiety. In vitro and animal models initially suggested that P57 mimics the effects of glucose on hypothalamic neurons. Normally, when blood glucose levels rise after a meal, glucose enters hypothalamic neurons and is metabolized, leading to an increase in the intracellular ratio of ATP to AMP. This rise in ATP closes ATP-sensitive potassium (K-ATP) channels, depolarizing the cell membrane and opening voltage-gated calcium channels. The resulting influx of calcium triggers the firing of pro-opiomelanocortin (POMC) neurons, which release alpha-melanocyte-stimulating hormone (α-MSH), a potent appetite suppressant.

Early research hypothesized that P57 could bypass the metabolic steps of glucose and directly increase intracellular ATP levels in these hypothalamic neurons by up to 50-150%. By artificially inflating ATP levels, P57 was thought to trick the brain into a state of perceived satiety, thereby drastically reducing the drive to consume food.

Pharmacokinetics: The Blood-Brain Barrier and Bioavailability Failures

While the in vitro mechanism of P57 appeared promising, the translation to human in vivo pharmacokinetics revealed catastrophic flaws. For a compound to exert central appetite-suppressing effects, it must survive first-pass metabolism in the liver, enter systemic circulation, and successfully cross the highly selective blood-brain barrier (BBB). P57 fails on multiple fronts. As a bulky steroidal glycoside, P57 is highly susceptible to enzymatic degradation in the gastrointestinal tract and rapid metabolism by hepatic cytochrome P450 enzymes.

More critically, the intact P57 molecule exhibits extremely poor permeability across the blood-brain barrier. Human clinical trials have demonstrated that oral ingestion of Hoodia gordonii extracts fails to achieve the central nervous system concentrations required to alter hypothalamic ATP ratios. Because the active molecule cannot reach its target receptors in the brain at therapeutic doses, the theoretical appetite-suppressing mechanism is rendered entirely inert in humans.

Toxicological Mechanisms and Off-Target Effects

The failure of Hoodia gordonii is compounded by its toxicological profile. In the lone independent randomized controlled trial assessing its efficacy, the dosage required to match the theoretical therapeutic threshold was found to be synonymous with the toxic dose observed in murine models. Supplementation with Hoodia gordonii extract was associated with a statistically significant increase in total bilirubin. Bilirubin is a byproduct of the normal breakdown of red blood cells; elevated levels can indicate either increased hemolysis (destruction of red blood cells) or hepatic stress, as the liver struggles to conjugate and excrete the compound.

Furthermore, Hoodia supplementation has been linked to increases in blood pressure and heart rate. While the exact mechanism for this cardiovascular stress is not definitively established, it is hypothesized to be related to off-target sympathetic nervous system activation or the presence of unidentified vasoactive alkaloids within the plant matrix. Additionally, the gastrointestinal distress (nausea, vomiting) frequently reported with Hoodia use may be a localized reaction to the high concentration of steroidal saponins, which are known to irritate the gastric mucosa.

The Adulteration Factor: Sibutramine and Synthetic Stimulants

Because genuine Hoodia gordonii is an endangered species that grows extremely slowly in the Kalahari Desert, the raw material is exceptionally rare and expensive. This economic reality, combined with the plant's lack of natural efficacy, has led to widespread adulteration in the supplement industry. Many products marketed as Hoodia have been found by the FDA to contain no actual Hoodia gordonii. Instead, they are frequently spiked with sibutramine, a synthetic, centrally acting serotonin-norepinephrine reuptake inhibitor (SNRI) that was banned from the global market in 2010 due to severe cardiovascular risks, including myocardial infarction and stroke. The presence of sibutramine artificially creates the appetite suppression and cardiovascular side effects (hypertension, tachycardia) that consumers mistakenly attribute to the Hoodia plant itself.

Questions About Hoodia Gordonii
What does hoodia do to your body? +
In clinical trials, Hoodia gordonii has been shown to have no significant effect on appetite suppression or weight loss. Instead, it may cause adverse effects such as increased blood pressure, elevated heart rate, nausea, and increased bilirubin levels, which can indicate liver stress.
What are the concerns with Hoodia gordonii? +
The primary concerns with Hoodia are its lack of efficacy, potential for mild toxicity (including cardiovascular and hepatic stress), and rampant product adulteration. Many commercial Hoodia products are counterfeit, and some have been found spiked with dangerous, banned pharmaceutical drugs like sibutramine.
What is Hoodia gordonii? +
Hoodia gordonii is a spiky, cactus-like succulent shrub native to the Kalahari Desert in southern Africa. It was traditionally chewed by the indigenous San Bushmen to stave off hunger and thirst during long hunting trips, which led to its commercialization as a weight-loss supplement.
Is Hoodia gordonii approved by the FDA? +
No, Hoodia gordonii is not approved by the FDA for weight loss or any other medical condition. In fact, the FDA has issued warnings against specific Hoodia products that were found to be adulterated with banned, dangerous substances.
Does hoodia raise blood pressure? +
Yes, clinical trials have demonstrated that supplementation with Hoodia gordonii extract can cause significant increases in both blood pressure and heart rate. This makes it particularly dangerous for individuals with pre-existing cardiovascular conditions.
What medications should you not take with Hoodia? +
You should avoid taking Hoodia if you are on blood pressure medications, heart medications, diabetes drugs, or blood thinners like aspirin, warfarin, or heparin. Hoodia's effects on blood sugar sensing and cardiovascular markers can cause dangerous interactions.
Does Hoodia actually suppress appetite? +
No. While it was theorized to suppress appetite by tricking the brain into feeling full, human clinical trials have proven that Hoodia extracts do not reduce caloric intake or promote weight loss compared to a placebo.
What is P57 in Hoodia? +
P57 is an oxypregnane steroidal glycoside found in the Hoodia plant. It is the active compound that researchers believed was responsible for appetite suppression, though studies later showed it cannot effectively cross the human blood-brain barrier.
Why is Hoodia considered an endangered species? +
Hoodia gordonii grows extremely slowly in the harsh conditions of the Kalahari Desert. The massive surge in global demand for Hoodia as a weight-loss supplement led to severe over-harvesting, threatening the wild populations and leading to strict international trade protections.
Can Hoodia cause liver damage? +
Clinical studies have shown that Hoodia supplementation can lead to elevated levels of bilirubin in the blood. While not definitive proof of severe liver damage, elevated bilirubin is a biomarker for hepatic stress or red blood cell destruction, indicating mild toxicity.
Are Hoodia supplements fake? +
A large percentage of Hoodia supplements on the market are counterfeit. Because genuine Hoodia is rare and expensive, many products contain cheap fillers like prickly pear cactus or are entirely devoid of the active P57 compound.
Why did the FDA ban some Hoodia products? +
The FDA issued warnings and recalls for certain Hoodia products, such as 'P57 Hoodia', because laboratory testing revealed they contained sibutramine. Sibutramine is a synthetic weight-loss drug that was banned globally due to its risk of causing heart attacks and strokes.
What is sibutramine and why is it in Hoodia? +
Sibutramine is a banned pharmaceutical appetite suppressant known to cause severe cardiovascular issues. Unscrupulous manufacturers illegally spike fake Hoodia supplements with sibutramine to artificially create the weight-loss effects that the Hoodia plant fails to provide.
How did the San Bushmen use Hoodia? +
The nomadic San Bushmen of the Kalahari Desert traditionally sliced off the stem of the wild Hoodia plant and chewed it raw. They used it as a 'famine food' to suppress the sensations of hunger and thirst during grueling, multi-day hunting expeditions.
Is Hoodia a cactus? +
Despite its spiky, fleshy appearance, Hoodia gordonii is not actually a cactus. Botanically, it is classified as a succulent shrub belonging to the Apocynaceae family (the dogbane family).
What is the recommended dosage for Hoodia? +
There is no recommended dosage because Hoodia is proven to be ineffective and potentially toxic. Clinical trials used roughly 1,000 mg of purified extract per day, but this dose failed to cause weight loss and resulted in adverse side effects.
Can diabetics take Hoodia? +
Diabetics should strictly avoid Hoodia. The plant's active compound is theorized to interfere with how the brain senses glucose, which could unpredictably alter blood sugar regulation and interact dangerously with diabetes medications.
Does Hoodia interact with blood thinners? +
Yes, Hoodia is contraindicated for individuals taking blood-thinning medications such as warfarin, heparin, or aspirin. It may interfere with blood clotting mechanisms, increasing the risk of bleeding disorders.
Research Highlights
Blom WA, et al., 2011RCT
Effects of 15-d repeated consumption of Hoodia gordonii puri
The extract failed to reduce ad libitum energy intake or body weight compared to placebo, and was associated with significant increases in blood pressure, heart rate, and bilirubin levels, indicating mild toxicity.
Deep Content
Everything About Hoodia Gordonii Article

The Legend of Hoodia Gordonii: From the Kalahari to the Supplement Aisle

For decades, the weight-loss industry has been on a relentless quest to find the ultimate natural appetite suppressant. In the early 2000s, the spotlight turned to the harsh, arid landscapes of the Kalahari Desert in southern Africa. Here grows Hoodia gordonii, a spiky, cactus-like succulent (though botanically a shrub) that produces tan flowers with a notoriously unpleasant odor.

The sudden global interest in this obscure plant was sparked by the traditional practices of the San Bushmen, an indigenous nomadic people. Anthropologists noted as early as 1937 that the San people would slice off the stem of the Hoodia plant and chew it to stave off the agonizing pangs of hunger and thirst during multi-day hunting expeditions in the sparsely vegetated desert. This historical use as a "famine food" was all the marketing material the dietary supplement industry needed. Almost overnight, Hoodia gordonii was hailed as a miracle weight-loss cure, promising to effortlessly shut down the human appetite.

However, the transition from a raw plant chewed in the desert to a processed extract in a plastic bottle revealed a stark contrast between traditional folklore and clinical reality. Today, rigorous scientific scrutiny has largely debunked the claims surrounding Hoodia, exposing a trail of failed clinical trials, alarming side effects, and rampant industry fraud.

The Biochemistry of P57: A Flawed Mechanism

To understand why Hoodia gordonii became so popular, one must look at the science that initially supported it. Researchers isolating the compounds within the plant discovered a unique oxypregnane steroidal glycoside, which they named P57.

In laboratory settings, P57 appeared to be a groundbreaking discovery. The human brain regulates hunger primarily through the hypothalamus. After you eat a meal, blood glucose levels rise, and this glucose enters the hypothalamic neurons. The metabolism of glucose increases the intracellular ratio of ATP (energy) to AMP. This spike in ATP acts as a signaling mechanism, telling the brain that the body is fed, which triggers the release of appetite-suppressing hormones.

In vitro studies suggested that P57 could bypass the need for actual food. It appeared to directly increase ATP levels in hypothalamic neurons by up to 150%, effectively tricking the brain into a state of perceived fullness. On paper, P57 was the perfect appetite suppressant: it mimicked the satiety signals of a large meal without contributing a single calorie.

The Blood-Brain Barrier Problem

The fatal flaw of Hoodia gordonii lies in its pharmacokinetics—specifically, how the human body processes the P57 molecule. For P57 to trick the hypothalamus, it must first survive the digestive tract, pass through the liver, enter the bloodstream, and finally cross the blood-brain barrier (BBB).

The blood-brain barrier is a highly selective semipermeable border that prevents circulating toxins and large molecules from entering the central nervous system. P57 is a bulky, complex steroidal glycoside. Clinical pharmacokinetic studies have definitively shown that P57 has abysmal oral bioavailability. It is rapidly degraded by liver enzymes, and the fraction that does survive cannot easily penetrate the blood-brain barrier. Consequently, the concentration of P57 required to alter ATP levels in the hypothalamus is never reached in humans following oral supplementation. The mechanism that worked so beautifully in a petri dish completely fails in the human body.

Clinical Evidence: The Nail in the Coffin

The ultimate test for any dietary supplement is a randomized, double-blind, placebo-controlled human trial. For Hoodia gordonii, the definitive study was published in 2011 by Blom and colleagues.

The researchers recruited 49 healthy, overweight women and administered either a placebo or a highly purified Hoodia gordonii extract (standardized to contain over 70% steroidal glycosides) for 15 days. The dosage used was approximately 1,110 mg per day, taken before meals. The study meticulously tracked the participants' ad libitum energy intake (how much they chose to eat), body weight, and various safety markers.

The results were unequivocally negative. The women taking the Hoodia extract experienced zero significant reduction in their daily caloric intake compared to the placebo group. Furthermore, there was no difference in weight loss between the two groups. The study proved that even when using a highly purified, clinically standardized extract, Hoodia gordonii does not suppress appetite in humans.

Safety and Toxicity Concerns

The failure to induce weight loss was only half of the bad news from the 2011 clinical trial. The researchers also uncovered alarming safety signals.

Participants taking the Hoodia extract experienced a statistically significant increase in total bilirubin levels. Bilirubin is a yellowish pigment produced during the normal breakdown of red blood cells; elevated levels can indicate hepatic (liver) stress or increased hemolysis (red blood cell destruction).

Additionally, the Hoodia group experienced notable increases in both blood pressure and heart rate. This cardiovascular stress is particularly dangerous given that the target demographic for Hoodia supplements—overweight and obese individuals—are already at an elevated risk for hypertension and heart disease. Other reported side effects included nausea, vomiting, and strange skin sensations.

Examine.com, a leading independent authority on supplement science, notes a grim reality regarding Hoodia's safety profile: the dosage required to even attempt to reach therapeutic levels in humans is virtually identical to the dose that causes toxicity in mice.

The Adulteration Epidemic and FDA Warnings

Beyond the inherent ineffectiveness and toxicity of the plant itself, consumers face another massive risk: industry fraud.

Hoodia gordonii is an endangered species. It grows incredibly slowly, taking years to reach maturity in the harsh conditions of the Kalahari Desert. Due to over-harvesting driven by the supplement craze, international trade of Hoodia is now strictly regulated by CITES (the Convention on International Trade in Endangered Species of Wild Fauna and Flora).

Because genuine Hoodia is rare, expensive, and heavily regulated, the vast majority of "Hoodia" products sold online and in retail stores are completely counterfeit. Independent laboratory analyses have repeatedly shown that many commercial Hoodia supplements contain absolutely no P57. Instead, manufacturers fill the capsules with cheap fillers like prickly pear cactus, maltodextrin, or ordinary dietary fiber.

More maliciously, some manufacturers have spiked their fake Hoodia products with illegal pharmaceutical drugs to artificially create the weight-loss effect consumers expect. In 2011, the FDA issued a severe public warning regarding a product called "P57 Hoodia." Laboratory testing revealed that the product contained sibutramine, a dangerous, centrally acting weight-loss drug that was pulled from the global market in 2010. Sibutramine is known to substantially increase blood pressure and pulse rate, presenting a life-threatening risk to patients with a history of coronary artery disease, congestive heart failure, arrhythmias, or stroke.

Conclusion: A Supplement to Avoid

The story of Hoodia gordonii is a cautionary tale about the dangers of extrapolating traditional folklore and preliminary animal research into human dietary supplements.

While the San Bushmen may have found utility in chewing the raw plant for survival in the desert, modern science has definitively shown that oral Hoodia extracts do not work for weight loss. The active compound, P57, cannot reach the brain to suppress appetite. Worse, the doses required to even attempt efficacy result in cardiovascular stress and potential liver toxicity. When combined with the rampant fraud and dangerous adulteration in the Hoodia market, the conclusion is clear: Hoodia gordonii holds no promise as a dietary supplement and should be strictly avoided by consumers seeking safe and effective weight management solutions.

📱Questions about Hoodia Gordonii?
Text us your goals. We'll match you to the right product and dose.
Real humans + SuppVault AI · Msg rates apply · Reply STOP
← Back to Supplement Periodic Table
Shop All 1 Products with Hoodia Gordonii →