Cissus quadrangularis

Cissus quadrangularis is a traditional medicine for joint and bone health (as well as various feminine disorders and menopause), and shows promise in promoting bone growth rates. It is popular as a joint aid for athletes, with preliminary evidence supporting this property of cissus.

This page features 61 unique references to scientific papers.


All Essential Benefits/Effects/Facts & Information

Cissus quadrangularis is a traditional medicine usually said to come from Ayurveda but appears to have a wide range of locations which have used it medicinally due to it growing in numerous locations. Its traditional usages are mostly catered around treating feminine disorders (menopause, libido, and menstrual disorders) or treating bones (increasing bone mass or accelerating fracture healing rates) which gives it the traditional name of the 'Bone Setter'; some other traditional usages are in regards to its supposed antiulcer properties, antihemhorroid properties, and pain relieving properties.

It is most frequently used by athletes, and the anecdotes of cissus seem to precede much of the science on the topic. It appears to be a very effective pain killer in rodent studies, but at this moment in time only one preliminary study has been conducted in humans; while it showed promise in athletes who experienced joint pain due to exercise (by reducing overall joint symptoms by about a third) it was still a lone study. More research is needed, but it seems promising as an alterative for joint pain in athletes since most Joint Health supplements do not have evidence in athletes (rather, most research is in osteoarthritis persons).

Although a potential complication in athletes is that preliminary rodent evidence suggests that cissus has sedative and muscle relaxing properties at high doses (active within 30 minutes of ingestion), suggesting that it might not make the best pre-workout supplement.

In regards to bone health, there are limited human reports of increased fracture healing rate which are poor quality of evidence due to not disclosing adequate methodlogy (ie. how they did the study) and not disclosing the source of the compound. Animal studies do show a great deal of promise in promoting bone growth, but this traditional claim also needs to be assessed in greater detail.

Finally, there are two human studies which suggest that cissus can be used as a fat loss agent but they have problems with their structure. In particular both studies are confounded with possible financial biases and since the supplements were consumed before meals with water (and cissus is known to have gum forming properties) while food intake was not measured making it wholly possible the observed effects could be due to reduced food intake, which is what happens when a gum (glucomannan, for example) is taken before a meal with water.

Overall, cissus has a good deal of promise in regards to joint and bone health in regards to athletic adults and menopausal women alike but requires a great deal more evidence to fully evaulate this promise.

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Things To Know

Also Known As

Harjor, Asthi Shrinkhala, Bone Setter

Things to Note

  • Cissus may have muscle relaxing properties (estimated to occur with 20-40mg/kg of the water extract in humans) active within 30 minutes, suggesting it may not make a good preworkout

How to Take

Recommended dosage, active amounts, other details

The one study to note benefit with oral supplementation in humans (for the purpose of reducing joint pain) has used 3,200mg of cissus quadrangularis as a daily supplement, which is also in the range for what animal studies suggest sedative and pain killing effects should occur with the water extract.

Elsewhere, 300-600mg of a cissus quadrangularis extract standardized to 2.5% ketosteroids has shown biological activity in humans.

Either of the two aforementioned doses should work (former probably more relevant for athletes), but the optimal dose is not known as this moment in time.

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Human Effect Matrix

The Human Effect Matrix looks at human studies (it excludes animal and in vitro studies) to tell you what effects cissus quadrangularis has on your body, and how strong these effects are.

Grade Level of Evidence
Robust research conducted with repeated double-blind clinical trials
Multiple studies where at least two are double-blind and placebo controlled
Single double-blind study or multiple cohort studies
Uncontrolled or observational studies only
Amount of Evidence
? The amount of high quality evidence. The more evidence, the more we can trust the results.
Outcome Magnitude of effect
? The strength of the outcome. Some supplements can have an increasing effect, others have a decrease effect, and others have no effect.
Consistency of research results
? Scientific research does not always agree. HIGH or VERY HIGH means that most of the scientific research agrees.
Plasma Serotonin Notable Very High See study
Increase in plasma serotonin was significant (30-39%) and fairly noteworthy, deserves more research.
Creatinine Minor Very High See study
An increase in creatinine has been noted alongside weight loss; practical significance of this information is not known.
Lipid Peroxidation Minor Very High See study
A minor reduction in lipid peroxidation has been seen in serum associated with weight loss; uncertain significance.
Total Cholesterol Minor Very High See study
Reductions in total cholesterol not overly remarkable relative to placebo and confounded with weight loss which occurred with cissus
Triglycerides Minor Very High See study
Reduction in triglycerides is not overly potent and occurred alongside weight loss, which was likely a confounding factor.
Weight Minor Very High See study
There may be a small weight loss associated with 300mg cissus (2.5% ketosteroids) which was seen alongside a reduction in appetite in obese persons; no known direct fat burning properties.
Hemorrhoids - Very High See study
Although some traditional usage of the herb suggests otherwise, limited (accessible) human data does not support a role for cissus in the treatment of hemhorroids
Functionality in Elderly or Injured Notable Very High See study
An increase in the function of the joint appears to occur alongside reductions in perceived pain and soreness when cissus treats athletic joint pain; one of the few options that sees to benefit athletes.
Pain Notable Very High See study
Joint pain appears to be reduced following supplementation of cissus, and while the magnitude is not remarkable (respectable, but comparable to other supplements) it seems to be one of the few validated in athletes with nonpathological joint pain.
Blood Pressure - Very High See study
In otherwise healthy athletic men, there is no significant influence of supplementation over eight weeks on blood pressure.
Bone Healing Rate - Very High See study
More evidence is required, as the one study noting that cissus was ineffective in isolation noted that combination therapy with cissus and calcium was quite effective. There may be a role of Cissus, but it currently is not demonstrated
Heart Rate - Very High See study
No significant influence on heart rate when taken over the course of eight weeks.

Scientific Research

Table of Contents:

  1. 1 Sources and Composition
    1. 1.1 Sources
    2. 1.2 Composition
  2. 2 Neurology
    1. 2.1 GABAergic Neurotransmission
    2. 2.2 Sedation
    3. 2.3 Epilepsy and Convulsion
    4. 2.4 Analgesia
  3. 3 Cardiovascular Health
    1. 3.1 Endothelium
  4. 4 Interactions with Glucose Metabolism
    1. 4.1 Type II Diabetes
  5. 5 Obesity and Body Mass
    1. 5.1 Interventions
  6. 6 Skeletal Muscle and Physical Performance
    1. 6.1 Power Output
  7. 7 Bone and Joint Health
    1. 7.1 Osteoblasts
    2. 7.2 Joints
    3. 7.3 Fractures
    4. 7.4 Bone Loss
  8. 8 Interactions with Hormones
    1. 8.1 Estrogen
    2. 8.2 Cortisol
    3. 8.3 Testosterone
  9. 9 Inflammation and Immunology
    1. 9.1 Macrophages
    2. 9.2 Allergies
  10. 10 Interactions with Organs
    1. 10.1 Stomach
    2. 10.2 Liver
    3. 10.3 Intestines
  11. 11 Pregnancy and Sexuality
    1. 11.1 Libido
    2. 11.2 Pregnancy
  12. 12 Safety and Toxicity
    1. 12.1 General
    2. 12.2 Genotoxicity

1Sources and Composition

1.1. Sources

Cissus quadrangularis (of the family vitaceae) is a joint and bone health herb (known to 'accelerate the rate of bone healing'[1]) from Ayurveda under the name of Asthi Shrinkhala (Sanskrit)[2] with is also used for treatment of digestive, asthmatic, and menstrual disorders as well as the health of the eyes and ears[3][1] and less frequently for muscle pain (both smooth and contractile).[4][5] The plant is known to grow indigenously in India, Malaysia, Sri Lanka, Thailand, and Africa where it is used medicinally and bears other names such as hadjod (Hindi) and 'Bone Setter' in reference to its bone healing properties.[6]

Cissus quadrangularis is a traditional medicine for female health and for the health/function of both bones and joints, with some minor uses in digestive health

1.2. Composition

Cissus quadrangularis (aerial parts unless otherwise specified) tend to contain:

  • 6′-O-trans-cinnamoyl-catalpol, 6-O-{2,3-dimethoxy}-t-cinnamoyl-catalpol, and 6-O-m-methoxy-benzoyl catalpol (acetylated glycosides of catalpol)[7][8]
  • Friedelin (pentacyclic triterpenoid), possibly up to 2.5% in 70% ethanolic extracts of the aerial parts (IND-HE)[9][6]
  • Two isomeric ketosteroids, onocer-7-ene-3α,21β-diol and onocer-7-ene-3β,21α-diol[10] and some others including 7-oxoonocer-8-ene-3β,21α-diol[10]
  • δ-amyrin and δ-amyrone[11][10]
  • 3,3',4,4'-tetrahydroxybiphenyl[10]
  • Quercetin (0.007634-0.042649%[12]) and Kaempferol[11]
  • Stilbene compounds such as Resveratrol (0.000264-0.000676%[12]) or Piceatannol,[13] resveratrol glycosides,[11] and other stilbenes such as pallidol, parthenocissine A, and quadrangularin A-C (both resveratrol dimers)[7][13] genistein and daidzein[7]
  • Vitamin C at around 327mg per 100g[14]
  • Vitamin E at around 696mg per 100g[14]
  • β-sitosterol (1.15% methanolic extract, 0.5% ethyl acetate extracts, undetectable in water[15]) and stimasterol (0.47%, 0.16%, and undetectable respectively[15])

The main molecules of concern here seem to be the triterpenoids, where the very unique looking 'asymmetrical tetracyclic triterpenoids' (usually called ketosteroids) and freidelin seem active. Other bioactives may include the stilebenes such as resveratrol (and its unique dimers, such as Quadrangularin A) and the molecules based off of catalpol

Cissus Quadrangulus extract (stem) has an anti-oxidative phenolic capacity of 585.40+/-0.16mg gallic acid equivalents (GAE) per 100g[14] which are thought to underlie some of the observed antioxidant effects[14][16] and also contains a 16.2mg/kg alkaloid content (expressed by dry weight of the plant).[17] Flavonoid content is 169.2+/-1.97mg QE (Quercetin equivalent) per 100g.[17]

Cissus species of plants possess a gum (oleoresin) similar to some other nutritional herbs such as Irvingia gabonensis or khaya grandifoliola,[18] and these gums normally serve roles in either rapidly absorbing water in solution (demonstrated with khaya gum[19]) or causing coingested drugs to have a time-release; this is thought to be the reason it has been used with the intent of an appetite suppressant.[20][21]

The plant has a general antioxidant capacity (not overly impressive relative to some other herbs or pure antioxidants)


2.1. GABAergic Neurotransmission

The whole plant of cissus quadrangularis (methanolic extract) appears to have relatively low binding affinity to the GABAA benzodiazepine site in the concentration range of 0.1-10mg/mL.[22]

While there are some GABAergic properties thought to occur due to the enhancement of sleep time induced by diazepam (see the sedation section), there is currently a lack of information on what bioactives are working and how they are working

2.2. Sedation

When tested in a model of diazepam induced sleep, cissus quadrangularis (250-500mg/kg of the water extract) in mice appears to reduce sleep latency (by 47%) and prolong time asleep (a 10-fold increase from 21+/-8 minutes to 215+/-38 minutes) relative to the diazepam control at the higher dose only.[4]

There appears to be an enhancement of benzodiazepine induced sleep time seen with cissus quadrangularis oral intake in high but reasonable doses, suggesting an enhancement of GABAA signalling

2.3. Epilepsy and Convulsion

250-500mg/kg of the water extract fed to mice an hour before seizure induction (Isonicotinic Hydrazide Acid (IHA) or electrical shock) was reported to reduce convulsions by 60-75% (electric shock) and delay seizures by 36-77% (IHA), both of which were significantly protective but less than the reference drug of 10mg/kg diazepam (83% reduction and 117% delay, respectively).[4]

There appears to be respectable anticonvulsive properties associated with this plant based on preliminary animal evidence

2.4. Analgesia

The early phase of the formalin test (analgesic test) has shown benefit from cissus quadrangularis (10-40mg/kg of the methanolic extract; 11.82% yield) by inhibiting 22-47% of the licking response, outperforming the reference drug of aspirin (300mg/kg; 28%) despite aspirin being significantly more effective in the late phase (96% relative to 33-68%).[23] There is also analgesia in the acetic-acid writhing test, with 10-40mg/kg exerting 34-72% inhibition while aspirin reached 66%[23] and the water extract (250-500mg/kg; orally) has shown efficacy in a hot plate test with similar potency over 90 minutes.[4]

In animal testing, cissus quadrangularis appears to be effective in reducing pain at oral doses low enough to be feasible with oral supplementation in humans

These analgesic effects have been noted in exercise trained men reporting (nonpathological) joint pain associated with exercise, where supplementaiton of 3,200mg of a cissus quadrangularis supplement reduced joint pain as assessed by the WOMAC rating scale (no placebo control nor reference drug for comparison).[24]

Preliminary human evidence supports a pain killing effect in athletic persons associated with oral intake of the extract

3Cardiovascular Health

3.1. Endothelium

In isolated endothelial cells (ECV304) cissus quadrangularis appears to be able to reduce H2O2 mediated oxidative damage with an IC50 of 7.49+/-0.20mg/mL and secondary to this protective effect there was an increase in antioxidant enzymes and eNOS activity;[12] this was thought to be due to the low Resveratrol and Quercetin content, as both molecules were significantly more protective.[12]

Some possible, but not overly potent nor relevant, protective effects on the endothelium thought to be mostly due to two other dietary supplements which are minor components of cissus

4Interactions with Glucose Metabolism

4.1. Type II Diabetes

Supplementation of cissus quadrangularis methanolic extract at 10% of an obesogenic diet over 60 days appears to be able to attenuate the increases in blood glucose and insulin, as well as improve insulin sensitivity, with a comparable potency to Metformin;[14] there was no signifiant influence of cissus treatment to normal rats, and the dose may be too impractically high to be seen with standard oral supplementation of cissus in humans.

At this moment in time, there is no significant nor relevant antidiabetic properties demonstrated with standard doses of the supplement and higher oral doses seem to confer some protective effects in overfed rats (common to many supplements)

5Obesity and Body Mass

5.1. Interventions

In a sample of obese persons (n=72), 300mg Cissus daily standardized to 2.5% ketosteroids was able to reduce body fat levels from 33.07+/-10.26% to 30.81+/-5.92% by 4 weeks and 28.23+/-6.12% by 10 weeks, in which only 10 weeks was significantly different than placebo.[20] This dose was able to reduce body weight by 8lbs over 10 weeks, and was slightly more effective when paired with Irvingia gabonensis.[20]

Another study utilizing Cissus (standardized to 2.5% ketosteroids and 15% fiber) but with other confounds in the same capsules (Green Tea Catechins and B-vitamins) found that obese persons had a weight reduction of 6.9% over 8 weeks and overweight persons 4.8% over the same time period; pairing a 2200kcal diet with the supplement in obese persons resulted in 8.5% body weight reduction.[21] Obese persons lost 6% of their body fat and overweight persons 4.7% without diet.[21] Another study using this same formulation found similar results, although did not have a group taking only Cissus without a dietary intervention.[25]

At this moment in time, most studies on cissus quadrangularis and fat reduction are conducted in obese persons in which a reduction in food intake (and thus weight loss due to less food intake) cannot be ruled out. Due to this, the potential influence of study financing, and no plausible mechanism for cissus to reduce fat supplementation of cissus for the purpose of fat loss does not seem overly promising

6Skeletal Muscle and Physical Performance

6.1. Power Output

250-500mg/kg of the water extract appears to have muscle relaxant properties within 30 minutes of oral ingestion in mice as assessed by a rotarod test, with the higher dose being nonsignificantly less impairing than 5mg/kg diazepam.[4]

High doses of the water in mice (correlating to around 20-40mg/kg in humans, a feasible dose) appear to have muscle relaxing properties alongside the sedative propertis which can act 30 minutes after oral ingestion; while not shown to work in humans yet, it may be prudent to not take cissus as a pre-workout supplement due to this

7Bone and Joint Health

7.1. Osteoblasts

In SaOS-2 osteoblasts, cissus quadrangularis (water extract of the aerial parts) at 1-10μg/mL was able to concentration-dependnetly increase the basal secretion of IGF-1 (mRNA increased by 42.6-69.26% and protein levels by 38.4-84.6%), IGF-II (mRNA by 35.51-77.95% and protein by 71.43-104%), and there was also an increase the expression of the IGF receptor with the mRNA being increased by 50.66-62.66% whereas the actual receptor content was increased by 27.39-67.8%;[26] while there was no increase in the mRNA levels of the IGF binding protein which suppresses IGF activity (IGFBP-3), there was an increase in the protein content by 28.47-52.89% in the same concentration range.[26]

These effects may be related to either the estrogenic properties of cissus quadrangularis (as estrogen itself can increase IGF secretion from osteoblasts[27]) but this has not yet been confirmed.

There appears to be a concentration dependent increase in the secretion of insulin-like growth factors in osteoblasts at a concentration range which seems feasible to occur following oral ingestion

Cissus quadrangularis (ethanolic extract of aerial parts) at a range of 0.1-100µg/mL noted that there was no time-dependent increase in the proliferation of SaOS-2 osteoblasts at 0.1µg/mL (100nM) where proliferation was increased by 14-21%, but at 10µg/mL there was a time-dependent increase reaching 68-80% peaking after 48 hours.[28]

Differentiation of osteoblasts also occurs in the active range due to an increase in alkaline phosphatase (ALP) secretion at 1-10µg/mL or the water extract (53-105% increase in mRNA[28]) or 100-300µg/mL of the petroleum ether extract[29] alongside an increase in the mRNA of RunX2 (66-118%) as well as its transcriptional activity with the water extract;[28] the increase in ALP activity seems due to MAPK activation, mostly p38.[30] And both mineral nodule formation and mineralization have been noted to be increased under the influence of cissus quadrangularis.[28][30]

Elsewhere, the differentiation of mesenchymal stem cells into osteoblasts also appears to be enhanced with incubation of cissus (100-300µg/mL of the petroleum ether extract) in a manner that is additive with estrogens.[29]

The proliferation of osteoblasts may be related to 6′-O-trans-cinnamoyl-catalpol which has been noted to have osteogenic activity by itself, which was active in the range of 1-1,000pM and similarly effective to rutin from allophylus serratus and a few phenolics in vitex negundo similar in structure to the one in cissus.[8]

It seems that the extracts from cissus quadrangularis can promote osteoblastic proliferation and differentiation, and may influence the promotion of mesenchymal stem cells into osteoblasts

7.2. Joints

Collagen synthesis (mRNA levels) appears to be increased with 1-10µg/mL cissus quadrangularis in SaOS-2 (osteoblast) cells, to the degree of 85-106% over baseline.[28]

Collagen synthesis has been noted to be increased in osteoblasts; significance to joints unknown

A study in exercise trained men who experienced chronic joint pain due to said exercise given 3,200mg of cissus quadrangularis daily for eight weeks noted that supplementation noted that supplementation was associated with a 31% reduction in total WOMAC score (self-reported joint pain and impairment) relative to baseline.[24]

Preliminary evidence in athletic men with joint injuries arising from exercise appears to support a role for cissus quadrangularis in reducing joint pain and improving mobility

7.3. Fractures

Cissus quadrangularis is famous in traditional medicine for healing bones, insofar that it is referred to as the 'bone setter'[6] and is commonly used for this purpose according to surveys of traditional medicine usage (Ghana);[31] while there has been a large amount of research in animal models that is seen as not relevant to humans (due to placing cissus quadrangularis directly into bone tissue during surgeries or injecting it[32][33][34][35][36]) there does appear to be one (preliminary) study in humans where in persons with mandibular fractures noted benefit in regards to reducing pain after a week of supplementation, but beyond that week and in all other parameters (swelling, tenderness, mobility) it was not significantly better than placebo over the course of six weeks.[37]

It is thought that the improvement in fractures is in part due to suppressing corticosteroid signalling (by acting as a receptor of the glucocorticoid receptor) and preserving anabolism of bone tissue, while also directly promoting osteoblastic proliferation and differentation;[33][32] these claims have not yet been fully proven in oral studies.

The bone healing properties of cissus quadrangularis are one of its most popular traditional claims, but at this moment in time there does not appear to be good human evidence to support the usage of cissus for this goal

7.4. Bone Loss

Oral intake of cissus quadrangularis (petroleum ether extract of the stem; 0.07% yield) in a rat model mimicking menopause (ovarectomized rats) at a dose of 500mg/kg for ninety days is able to fully prevent losses of bone strength and prevent up to 86% of the losses in bone thickness;[38] cissus quadrangularis showed comparable efficacy to 5.4mg/kg of the SERM known as raloxifene, and while this study is duplciated in Medline[39] the design has been replicated where a month of cissus quadrangularis supplementation (500mg/kg petroleum ether extract) was comparable in efficacy 25mg/kg raloxifene in ovarectomized rats.[40]

In mice, 500mg/kg cissus quadrangularis has been noted to reverse the ovarectomy induced increase in inflammatory cytokines (TNF-α) and augment the increase in IL-1β from 39% to 322%;[41] these changes were associated with near absolute preservation of corticol and cancellous bone mineral density and thickness.[41]

The aerial parts (stem and leaves) of this plant have been noted elsewhere to be effective, where 75-100mg/kg of a phytoestrogen rich extract (70% ethanolic with 2.5% friedelin) in ovarectomized rats was able to increased circulating estrogen and Vitamin D in serum while the higher dose was comparable to estrogen in promoting bone strength and thickness but not density.[9]

In rat studies, oral ingestion of various extracts of cissus quadrangularis appear to exert near maximal protection against the losses in bone strength seen with ovarectomy, although the one study measuring bone mineral density failed to find a significant protective effect of comparable potency

8Interactions with Hormones

8.1. Estrogen

In ovarectomized rats (a model of estrogen deficiency), oral supplementation of a 70% ethanolic extract (2.5% friedelin content) has been noted to increase estrogen relative to the ovarectomized control by 194% (75mg/kg) and 232% (100mg/kg) which were statistically significant but less than the reference drug of 17β-estradiol injections (568%);[9] despite the difference, both were comparable in preserving bone integrity.[9] This study is duplicated in Pubmed (due to the exact same magnitude of serum estrogen increases), where estrogenic effects were confirmed by vaginal histology and uterine weight.[6]

A 70% ethanolic extract of this plant appears to possess estrogenic properties related more to increasing serum estrogen rather than directly acting on estrogen receptors; practical significance in male rodents and humans not yet known

8.2. Cortisol

Compounds in Cissus Quadrangularis have been shown to act as glucocorticoid antagonists when placed in bone tissue (potency as assessed by IC50 values not given), which would reduce their catabolic effects by occupying the receptor.[33][32]

Potential role as a glucocorticoid antagonist (which would reduce the effects of cortisol) but this has not yet been linked to oral supplementation in any species

8.3. Testosterone

Due to the ability of cissus quadrangularis to act as a glucocorticoid antagonist, it has been proposed to possess anabolic/androgenic activity;[32] no studies have yet addressed this topic.

9Inflammation and Immunology

9.1. Macrophages

Cissus quadrangularis ethyl acetate extract has been noted to suppress LPS induced activation of macrophages in the 50-400μg/mL range (IC50 of 53.88μg/mL; full suppression of nitrite production at 400μg/mL)[42] and the acetone is associated with inhibiting most inflammatory enzymes such as COX1 (IC50 of 106.46μg/mL), COX2 (25.9μg/mL), and 5-LOX (550μg/mL).[43] These antiinflammatory effects seem to be partly mediated by induction of heme-oxygenase 1 (HO-1) since inhibiting HO-1 attenuated the antiinflammatory effects seen with cissus ethyl acetate[42] but since not all was prevented it suggests that the enzyme inhibitors in the acetone extract may be independently active.[43]

The acetone extract has been further purified to an AFCQ extract, with more potent inhibitory properties on COX1 (IC50 of 7μg/mL), COX2 (400ng/mL), and 5LOX (20μg/mL) and comprised of mostly tannin structures.[43] This purified extract had an IC50 value of 65μg/mL in reducing LPS induced nitrite formation,[43] similar to the ethyl acetate extract elsewhere[42] which is less potent on the aformentioned enzymes.

It appears that cissus quadrangularis contains antioxidant compounds that activate HO-1 which then suppresses inflammation, but also contains some currently unknown tannin-like structures that are potent COX inhibitors when tested in vitro; both of these mechanisms are thought to underlie antiinflammatory effects

9.2. Allergies

The crude powder of cissus quadrangularis given to rats at the dose of 500-2,000mg/kg bodyweight one day and then again one hour before a carrageenin injections noted that the middle dose (1,000mg/kg) was able to significantly reduce the early phase swelling (indicative of histamine release) by 44%, outperforming 15mg/kg hydrocorticone.[44]

Some very limited evidence suggests a respectable antihistamine effect, but this has not been replicated and the application of cissus as an antiallergic compound is still ambiguous (due to a lack of information on mast cells and T cells)

10Interactions with Organs

10.1. Stomach

Cissus quadrangularis appears to have proton pump inhibitory (PPI) properties when the methanolic extract is tested in vitro of a potency (IC50 in inhibiting the H+/K+ ATPase pump of 38μg/mL) similar to omeprazole (reference at 26μg/mL).[17]

Cissus quadrangularis methanolic extract appears to have the ability to act as a proton pump inhibitor

In vitro, water extracts of cissus quadrangularis appear to have antibacterial properties against helicobacter pylori with MIC values in the range of 40μg/mL pending on when the plant said extract was derived from.[45]

May have some protective effects against helicobacter pylori infections, practical significance of this information is not yet known

Pretreatment of cissus quadrangularis before ulceration by NSAID drugs appears to be nearly prevented with 250-500mg/kg of the methanolic extract associated with normalization of the damaged occurring to the gastric wall[46] and reducing inflammatory and oxidative DNA damage seen in the stomach with NSAID ulceration.[47] 1,000mg/kg of this extract for a week prior to ulceration from aspirin (NSAID) has been noted to normalize ulceration to control levels, a potency similar to 30mg/kg rantidine (pharmaceutical PPI) by reducing ulceration 71.2-71.9%.[48][49]

Cissus has shown accelerated healing against ulcer formation induced by acetic acid when cissus was given at 250-500mg/kg of a methanolic extract (3.2% yield) the day after ulceration and for one week afterwards, where cissus performed equally to the reference drug sucralfate;[50] these rehabilitative effects were seen alongside an increased polyamine content, cell proliferation, and thymidine uptake in the gastric fluid of treated rats associated with a preservation of TGF-α.[50] Polyamines themselves are known to be highly rehabilitative in regards to ulcers (reducing polyamines reduces the healing rate[51]) and TGF-α is also a gastroprotective factor.[52]

While the PPI properties of cissus quadrangularis are thought to play a role, the aforementioned 500mg/kg methanolic extract dosage (which is optimal, due to being more protective than 250mg/kg and 750mg/kg[49]) appears to be associated with less neutrophil infiltration into gastric tissue.[49][53]

While it hasn't been directly linked to the PPI properties of cissus, this herb appears to have relatively potent anti-ulcer properties when given in either a prevenative or rehabilitative manner based on preliminary animal evidence; the oral doses used in these studies seem to be higher than other studies (estimated human dose being 80-160mg/kg with the higher dose being optimal)

10.2. Liver

One study in rats has noted that cissus quadrangularus at 10% of the diet when they were fed an obesogenic diet (high fructose and high fat), supplementation over the course of 60 days was able to reduce the increase in hepatic peroxidation and liver enzymes in serum.[14] There was no influence on liver enzymes, lipid peroxidation, or the lipid/cholesterol content of rats on a normal diet given cissus.[14]

A lower dose has been used elsewhere, where 500mg/kg of the methanolic extract of cissus quadrangularus was able to reduce the liver damage done by rifampicin or isoniazid both with nonsignificantly less potency than 50mg/kg silymarins (from Milk Thistle).[54][55]

There appears to be a protective effect when high doses of the herb are ingested, but they may be too impractically high to be relevant

10.3. Intestines

Cissus quadrangularis appears to be a (Thai) traditional medicine for hemhorroids[23] and has been noted to be a venotropic agent when tested in isolated umbilical veins at a concentration of 100-400µg/mL which was similar in potency to 400µg/mL Daflon (a mixture of Diosmetin and Hesperidin at 9:1).[23] Venotropic agents such as Daflon (other popular ones being Horse Chestnut and Pycnogenol) are known to also confer anti-hemhorroid properties, but when tested in humans supplementation of cissus quadrangularis has failed to outperform placebo despite Daflon being effective.[56] There appears to be another study that cannot be located online reporting benefit with 500mg twice daily supplementation (reported vicariously through these two studies[23][57]).

Should theoretically be a venotropic agent (increases blood flow in veins) and has been traditionally used as such, but the one study showing benefit cannot be located online to evaluated and the one that is available online failed to find a significant therapeutic effect

11Pregnancy and Sexuality

11.1. Libido

When 75-100mg/kg of the 70% ethanolic extract (2.5% friedelin) is given to a menopausal model of rats (ovarectomized) appeared to have libido promoting effects when the rats were exposed daily for over two months, with greater effects after two months relative to one; there were no immediate effects notable, and it appeared to be less significant than the reference drug of 17β-estradiol.[6]

At least one study has noted pro-libido enhancing properties in ovarectomized rats. It is not certain if this will occur in rats not undergoing ovarectomy, since it may be due to an estrogen increase and it isn't certain if estrogen is increased in youthful female rats or humans

11.2. Pregnancy

One study using 500mg/kg of the petroleum ether extract in pregnant rats noted that supplementation from the beginning of the second trimester until delivery was able to enhance bone mass (corticol and trabecular) in the newborn pups relative to control;[58] this appears to have been reported previously with the ethanolic extract (750mg/kg),[59] but while no complications were noted in either study there was no in depth toxicity testing on the pups.[58][59]

Appears to promote bone growth in newborn pups when orally ingested by the mother starting from the second trimester, but insufficient toxicology testing has been conducted

12Safety and Toxicity

12.1. General

One toxicology study found that, when using CQR-300 in rats, that a dose of 2500mg/kg bodyweight for 90 days was not associated with any observable side-effects (and established the NOAEL at this level), although some non-toxic changes occurred in blood clotting parameters at the higher doses.[3] Previously, a rat study on dosages up to 3g/kg bodyweight over a period of 3 months did not find any abnormal effects of Cissus supplementation,[60] the last dose (3g/kg) being 100-fold greater than the human therapeutic dose equivalent, and also noted non-toxic changes in blood parameters such as RBC count and clotting time (all within normal physiological range). From these results, it is postulated that a dose of 150g Cissus Quadrangularis daily is free from observable side-effects.[3][60]

Elsewhere, investigating the petroleum ether extract which appears to concentration anti-osteoporotic effects has been noted to be safe up to 5,000mg/kg oral ingestion in acute toxicity studies (with a single dose not causing harm over 30 days of observation).[38]

Two human trials using Cissus at dosages of 300mg daily (from CQR-300) found no observable side-effects[25][21] and a pilot study of 3,200mg daily for eight weeks in exercise trained men has similarly failed to find adverse effects.[24]

Appears to be safe at the doses commonly consumed, as toxicity has not been recorded in animal studies or traditionally via Ayurveda. The human studies using 300mg daily did not experience any differences from placebo in regards to side-effects

12.2. Genotoxicity

Cissus has been shown to produce genotoxic effects in vitro using a concentration of 500 and 1000ug/plate.[61] Replicated these tests in revertant colonies failed to replicated the results, and in vivo tests do not show this method of damage.[3]

Some data has noted a potential genotoxic effect in bacteria, but has failed to be replicated; practical significance of this information at this moment in time is not known but it is thought to not be relevant due to no observed genotoxicity in rodent models

Scientific Support & Reference Citations


  1. Gupta AK, Shah N, Thakar AB Effect of Majja Basti (therapeutic enema) and Asthi Shrinkhala (Cissus quadrangularis) in the management of Osteoporosis (Asthi-Majjakshaya) . Ayu. (2012)
  2. Potu BK, Rao MS, Sirasanagandla SR Effect of Majja Basti (therapeutic enema) and Asthi Shrinkhala (Cissus quadrangularis) in the management of Osteoporosis (Asthi-Majjakshaya) . Ayu. (2012)
  3. Kothari SC, et al Safety assessment of Cissus quadrangularis extract (CQR-300): subchronic toxicity and mutagenicity studies . Food Chem Toxicol. (2011)
  4. Kumar R, et al CNS activity of aqueous extract of root of Cissus quadrangularis Linn. (Vitaceae) . J Diet Suppl. (2010)
  5. Udayakumar R, Sundaran M, Krishna R Mineral and biochemical analysis of various parts of cissus quadrangularis linn . Anc Sci Life. (2004)
  6. Aswar UM, et al Estrogenic activity of friedelin rich fraction (IND-HE) separated from Cissus quadrangularis and its effect on female sexual function . Pharmacognosy Res. (2010)
  7. Singh G, Rawat P, Maurya R Constituents of Cissus quadrangularis . Nat Prod Res. (2007)
  8. Kumar M, et al Anti-osteoporotic constituents from Indian medicinal plants . Phytomedicine. (2010)
  9. Aswar UM, Mohan V, Bodhankar SL Antiosteoporotic activity of phytoestrogen-rich fraction separated from ethanol extract of aerial parts of Cissus quadrangularis in ovariectomized rats . Indian J Pharmacol. (2012)
  10. Mehta M, Kaur N, Bhutani KK Determination of marker constituents from Cissus quadrangularis Linn. and their quantitation by HPTLC and HPLC . Phytochem Anal. (2001)
  11. Phytochemical Studies on Cissus quadrangularis Linn.
  12. Sapsrithong T, et al Cissus quadrangularis ethanol extract upregulates superoxide dismutase, glutathione peroxidase and endothelial nitric oxide synthase expression in hydrogen peroxide-injured human ECV304 cells . J Ethnopharmacol. (2012)
  13. Stilbene Derivatives from Cissus quadrangularis
  14. Chidambaram J, Carani Venkatraman A Cissus quadrangularis stem alleviates insulin resistance, oxidative injury and fatty liver disease in rats fed high fat plus fructose diet . Food Chem Toxicol. (2010)
  15. Shah UM, et al Development and Validation of a Simple Isocratic HPLC Method for Simultaneous Estimation of Phytosterols in Cissus quadrangularis . Indian J Pharm Sci. (2010)
  16. Chidambara Murthy KN, et al Antioxidant and antimicrobial activity of Cissus quadrangularis L . J Med Food. (2003)
  17. Yadav P, Ganeshpurkar A, Rai G In vitro H(+) -K(+) ATPase inhibitory potential of methanolic extract of Cissus quadrangularis Linn . Pharmacognosy Res. (2012)
  18. Odeku OA, Okunlola A, Lamprecht A Microbead design for sustained drug release using four natural gums . Int J Biol Macromol. (2013)
  19. Odeku OA, Fell JT Evaluation of khaya gum as a directly compressible matrix system for controlled release . J Pharm Pharmacol. (2004)
  20. Oben JE, et al The use of a Cissus quadrangularis/Irvingia gabonensis combination in the management of weight loss: a double-blind placebo-controlled study . Lipids Health Dis. (2008)
  21. Oben J, et al The use of a Cissus quadrangularis formulation in the management of weight loss and metabolic syndrome . Lipids Health Dis. (2006)
  22. Bah S, et al Antiplasmodial and GABA(A)-benzodiazepine receptor binding activities of five plants used in traditional medicine in Mali, West Africa . J Ethnopharmacol. (2007)
  23. Panthong A, et al Analgesic, anti-inflammatory and venotonic effects of Cissus quadrangularis Linn . J Ethnopharmacol. (2007)
  24. Bloomer RJ, et al Cissus quadrangularis reduces joint pain in exercise-trained men: A pilot study . Phys Sportsmed. (2013)
  25. Oben JE, et al The effect of Cissus quadrangularis (CQR-300) and a Cissus formulation (CORE) on obesity and obesity-induced oxidative stress . Lipids Health Dis. (2007)
  26. Muthusami S, et al Cissus quadrangularis augments IGF system components in human osteoblast like SaOS-2 cells . Growth Horm IGF Res. (2011)
  27. Mochizuki S, et al Effects of estriol on proliferative activity and expression of insulin-like growth factor-I (IGF-I) and IGF-I receptor mRNA in cultured human osteoblast-like osteosarcoma cells . Gynecol Endocrinol. (2005)
  28. Muthusami S, et al Effects of Cissus quadrangularis on the proliferation, differentiation and matrix mineralization of human osteoblast like SaOS-2 cells . J Cell Biochem. (2011)
  29. Potu BK, et al Petroleum ether extract of Cissus quadrangularis (Linn.) enhances bone marrow mesenchymal stem cell proliferation and facilitates osteoblastogenesis . Clinics (Sao Paulo). (2009)
  30. Parisuthiman D, et al Cissus quadrangularis extract enhances biomineralization through up-regulation of MAPK-dependent alkaline phosphatase activity in osteoblasts . In Vitro Cell Dev Biol Anim. (2009)
  31. Upadhya V, et al Ethnomedicinal plants used to treat bone fracture from North-Central Western Ghats of India . J Ethnopharmacol. (2012)
  32. Chopra SS, Patel MR, Awadhiya RP Studies of Cissus quadrangularis in experimental fracture repair : a histopathological study . Indian J Med Res. (1976)
  33. Chopra SS, et al Studies on Cissus quadrangularis in experimental fracture repair: effect on chemical parameters in blood . Indian J Med Res. (1975)
  36. UDUPA KN, PRASAD GC Cissus quadrangularis in healing of fractures. A clinical study . J Indian Med Assoc. (1962)
  37. Singh V, et al Clinical evaluation of cissus quadrangularis and moringa oleifera and osteoseal as osteogenic agents in mandibular fracture . Natl J Maxillofac Surg. (2011)
  38. Potu BK, et al Anti-osteoporotic activity of the petroleum ether extract of Cissus quadrangularis Linn. in ovariectomized Wistar rats . Chang Gung Med J. (2010)
  39. Potu BK, et al Evidence-based assessment of antiosteoporotic activity of petroleum-ether extract of Cissus quadrangularis Linn. on ovariectomy-induced osteoporosis . Ups J Med Sci. (2009)
  40. Potu BK, et al Effect of Cissus quadrangularis Linn on the development of osteopenia induced by ovariectomy in rats . Clin Ter. (2011)
  41. Banu J, et al Inhibition of Bone Loss by Cissus quadrangularis in Mice: A Preliminary Report . J Osteoporos. (2012)
  42. Srisook K, et al Anti-inflammatory effect of ethyl acetate extract from Cissus quadrangularis Linn may be involved with induction of heme oxygenase-1 and suppression of NF-κB activation . J Ethnopharmacol. (2011)
  43. Bhujade AM, et al Evaluation of Cissus quadrangularis extracts as an inhibitor of COX, 5-LOX, and proinflammatory mediators . J Ethnopharmacol. (2012)
  44. Begum VH, Sadique J Anti histaminic activity of cissus quadragularis . Anc Sci Life. (1999)
  45. Austin A, Jegadeesan M, Gowrishankar R In-vitro screening of cissus quadrangularis L. Variant ii against helicobacter pylori . Anc Sci Life. (2003)
  46. Jainu M, Vijai Mohan K, Shyamala Devi CS Gastroprotective effect of Cissus quadrangularis extract in rats with experimentally induced ulcer . Indian J Med Res. (2006)
  47. Jainu M, Devi CS Gastroprotective action of Cissus quadrangularis extract against NSAID induced gastric ulcer: role of proinflammatory cytokines and oxidative damage . Chem Biol Interact. (2006)
  48. Antiulcerogenic activities of the Methanolic extract of Cissus quadrangularis in wistar
  49. Jainu M, Mohan KV, Devi CS Protective effect of Cissus quadrangularis on neutrophil mediated tissue injury induced by aspirin in rats . J Ethnopharmacol. (2006)
  50. Jainu M, Vijaimohan K, Kannan K Cissus quadrangularis L. extract attenuates chronic ulcer by possible involvement of polyamines and proliferating cell nuclear antigen . Pharmacogn Mag. (2010)
  51. Shin VY, et al Cigarette smoke extracts delay wound healing in the stomach: involvement of polyamine synthesis . Exp Biol Med (Maywood). (2002)
  52. Yetkin G, et al The healing effect of TGF-alpha on gastric ulcer induced by acetylsalicylic acid in rats . Int J Pharm. (2004)
  53. Jainu M, Shyamala Devi CS Attenuation of neutrophil infiltration and proinflammatory cytokines by Cissus quadrangularis: a possible prevention against gastric ulcerogenesis . J Herb Pharmacother. (2005)
  54. Viswanatha Swamy AH, et al Evaluation of hepatoprotective activity of Cissus quadrangularis stem extract against isoniazid-induced liver damage in rats . Indian J Pharmacol. (2010)
  55. Swamy AH, et al Hepatoprotective Effect of Cissus quadrangularis Stem Extract Against Rifampicin-induced Hepatotoxicity in Rats . Indian J Pharm Sci. (2012)
  56. Panpimanmas S, et al Experimental comparative study of the efficacy and side effects of Cissus quadrangularis L. (Vitaceae) to Daflon (Servier) and placebo in the treatment of acute hemorrhoids . J Med Assoc Thai. (2010)
  57. Pharmacognostic and traditional properties of Cissus quadrancularis Linn -An overview
  58. Potu BK, et al Petroleum ether extract of Cissus quadrangularis (LINN) stimulates the growth of fetal bone during intra uterine developmental period: a morphometric analysis . Clinics (Sao Paulo). (2008)
  60. Subchronic toxicity of Cissus quadrangularis Linn
  61. Sivaswamy SN, et al Mutagenic activity of south Indian food items . Indian J Exp Biol. (1991)

(Common misspellings for Cissus quadrangularis include Quadrangulus, Quadranglus, Sissus, Cisus, Sisus, Sisis, Quadralangus, Quadralangis)

(Editors who contributed to this page include smoomaster, , , akabalik, )