Simmondsia chinensis

Simmondsia chinensis (Jojoba) is a commonly used skin health supplement that may have appetite suppressing effects.

This page features 15 unique references to scientific papers.

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1Sources and Summary

1.1. Sources

Simmondsia chinensis is a plant known as Jojoba (not to be confused with Jujube) which is native to the Sonora desert of North America.[1][2]

1.2. Composition

The seeds of Simmondsia chinensis are commonly processed to remove the fatty acids (Jojoba Oil) from the rest of the seeds (Jojoba Meal), with the former having market value as a cosmeticeutical and the latter usually seen as a waste product.

Components of Jojoba Oil, which comprise about half of the seeds by weight,[3] include:

  • Eicos-11-enol (47.3% total oil)[3]

  • Docos-13-enol (45.8% total oil)[3]

  • Tetracos-15-enol (6.0% total oil)[3]

  • Octadec-9-enol (0.9% total oil)[3]

  • The 4-methylsterols Obtusifoliol, Gramisterol, Citrostadienol, and Cycloeucalenol[3]

  • The 4-demethylsterols Campesterol, Stigmasterol, Sitosterol[4] and Isofucosterol[3]

  • Cycloartenol, 24-methylenecycloartenol, and Cyclobranol[3]

The sterols mentioned above (last three bullet points) comprise 0.4% of the oil by weight, and the division of sterols in this 0.4% is high in sitosterol (63%), 24-methylcholesterol (18%) isofucosterol (7%) and stigmasterol (7%).[3]

Components of Jojoba Meal include:

  • Simmondsin (aka. 2-cyanomethylene-3 hydroxy 4,5 dimethoxy cyclohexyl-d-glucoside[1])


2Neurology

2.1. Appetite

Simmondsin appears to have a marked suppressive effect on appetite, as the first toxicological investigation into Jojoba meal (after the oil was extracted) noted that 5-10% of Joboba meal in the diet reduced food intake to a degree where rats died from emanciation after 94 days.[5] It appears to exert its mechanism of action in the intestines, as injections of large doses of Simmondsin fail to suppress appetite (and also fail to exert toxicity, which occurs with high doses of Simmondsin).[6]

Simmondsin appears to have a same profile of effects after ingestion as Cholecystokinin,[7] and the satiety induced by oral Simmondsin appears to be abolished with the CCKA receptor antagonist Devazepide.[8] It did not appear to be direct activation of the receptor, but indirect through the Vagus Nerve; Vagotomy partially abolishes the effect.[9][8]

Simmondsin appears to interact with the Vagus Nerve in the intestines and vicariously through Cholecystokinin (CCK) receptors to suppress food intake

When lean rats are fed Simmondsin for 8 weeks up to 0.5% of the diet noted that 0.15% of the diet reduced weight gain by 6% while 0.5% lowered weight below that of baseline despite being fed ad libitum, noted after 1 week but then maintaining weight up to 7 weeks.[1] 0.25% has been tested in other studies in lean rats and shown efficacy.[10]

When obese rats are fed Simmondsin for 16 weeks at 0.25-0.5% of the diet, dose-dependent reductions in food intake and weight are noted with the respective doses reducing carcass weight after 16 weeks by 17% and 26%.[1] Obese rats appear to be more sensitive to appetite suppression relative to lean rats.[10]

This appetite suppressing effect has been noted in other species such as dogs,[11] and is commonly observed in toxicology tested[12][1][6] insofar it was been thought to result in death of some rats at very high doses via reductions in food intake.[5]

Appears to have repeated evidence for appetite suppression in rats, and the potency of low doses of Simmondsin appear to be quite remarkable


3Interactions with Aesthetics

3.1. Skin

The fatty acid component of Jojoba seeds is sometimes referred to as Jojoba Liquid Wax (JLW) or Jojoba Oil and is the fragment used in cosmetics,[3] and appears to have been used topically by native americans in the regions Simmondsia Chinensis grows (southern US and Mexico) for bruises and wound healing.[13]

The liquid wax of Jojoba has displayed wound healing mechanisms in vitro, where 0.5-1% JLW solution was able to increase the wound repair capabilities of fibroblasts and keratinocytes (via PI3K-Akt-mTOR, as it was abolished by rapamycin) and was effective as platelet lysate (clinically used wound dressing agent) in inducing repair mechanisms.[13]


4Safety and Toxicity

Ingestion of 750mg/kg isolated simmondsin for 14 weeks is sufficient to kill mice (5/8) with the remaining mice experiencing hepatotoxicity and intestinal hemorrhage.[6] Oddly, no appetetite suppression nor toxicity was noted with injections.[6]

Ingestion of 250mg/kg Simmondsin in rats for 5 days fails to find any toxicological signs in the pancreas, liver, intestines, testes, or kidneys.[12] Simmondsin up to 0.5% of the diet in lean rats for 8 weeks failed to alter the weight of the liver, and caused a slight increase in percent of kidney weight relative to body weight (absolute kidney weight did not change, and this study did not weight loss due to food intake reduction); the same lack of organ weight changes were noted over 16 weeks in obese rats.[1] Histological examination did not note any remarkable abnormalities.[1]

Pregnant rats fed Simmondin appear to reduce their own food intake, which was deemed the reason birth weight in the offspring was reduced; no other development abnormalities were noted.[14]

In regards to blood parameters, 0.5% of the diet as Simmondsin appears to be associated with reductions of red and white blood cells as well as total lymphocytes with no significant effects at lower doses;[1] replicated from a previous study using 0.5% Simmondsin for 52 days.[15] There did not appear to be alterations in blood clotting, and feeding Simmondsin for 8 weeks and then ceasing ingestion for 8 weeks reverses the decline.[1]

Scientific Support & Reference Citations

References

  1. Boozer CN, Herron AJ Simmondsin for weight loss in rats . Int J Obes (Lond). (2006)
  2. Wistrom C, et al Distribution of glassy-winged sharpshooter and threecornered alfalfa hopper on plant hosts in the San Joaquin Valley, California . J Econ Entomol. (2010)
  3. Content and Composition of Free Sterols and Free Fatty Alcohols in Jojoba Oil
  4. Identification of the trace components of jojoba oil
  5. Booth AN, Elliger CA, Waiss AC Jr Isolation of a toxic factor from jojoba meal . Life Sci. (1974)
  6. Verbiscar AJ, et al Detoxification of jojoba meal . J Agric Food Chem. (1980)
  7. Flo G, et al Comparison of the effects of simmondsin and cholecystokinin on metabolism, brown adipose tissue and the pancreas in food-restricted rats . Horm Metab Res. (1998)
  8. Cokelaere MM, et al Devazepide reverses the anorexic effect of simmondsin in the rat . J Endocrinol. (1995)
  9. Flo G, et al The vagus nerve is involved in the anorexigenic effect of simmondsin in the rat . Appetite. (2000)
  10. Flo G, et al Effects of simmondsin on food intake, growth, and metabolic variables in lean (+/?) and obese (fa/fa) Zucker rats . Br J Nutr. (1999)
  11. Hawthorne AJ, Butterwick RF The satiating effect of a diet containing jojoba meal (Simmondsia chinensis) in dogs . J Nutr. (1998)
  12. Investigation of possible toxicological influences of simmondsin after subacute administration in the rat
  13. Ranzato E, Martinotti S, Burlando B Wound healing properties of jojoba liquid wax: an in vitro study . J Ethnopharmacol. (2011)
  14. Cokelaere M, et al Teratological studies in defatted jojoba meal-supplemented rats . Food Chem Toxicol. (2001)
  15. THE DETRIMENTAL EFFECT OF SIMMONDSIN ON FOOD INTAKE AND BODY WEIGHT OF RATS