Weight Management References 35245

Samenuk D et al. Adverse cardiovascular events temporally associated with ma huang, an herbal source of ephedrine. Mayo Clin Proc. 77(1): 12-16, 2002. www.mayo.edu/proceedings.

Boozer CN et al. Herbal ephedra/caffeine for weight loss: a 6-month randomized safety and efficacy trial. Int J Obesity. 26: 593-604, 2002. www.nature.com/ijo.

Fugh-Berman A. Herb-drug interactions. Lancet. 355(9198):134-8, 2000. www.thelancet.com.

Waluga M et al. Cardiovascular effects of ephedrine, caffeine and yohimbine measured by thoracic electrical bioimpedance in obese women. Clin Physiol. 18(1):69-76, 1998. www.blackwell-synergy.com.

Andersen T, Fogh J. Weight loss and delayed gastric emptying following a South American herbal preparation in overweight patients. J Hum Nutr Diet. 14(3):243-50, 2001. www.blackwell-science.com.

Boozer CN et al. An herbal supplement containing ma huang-guarana for weight loss: a randomized, double blind trial. Int J Obes Relat Metab Disord. 25(3):316-24, 2001. www-us.ebsco.com/online/OnlineTitles.asp.

Morelli V, Zoorob RJ. Alternative therapies: Part I. Depression, diabetes, obesity. Am Fam Physician. 62(5):1051-60, 2000. www.aafp.org/afp.

Heymsfield SB et al. Garcinia cambogia (hydroxycitric acid) as a potential antiobesity agent: a randomized controlled trial. JAMA. 280(18):1596-600, 1998. www.jama.com.

Mattes RD, Bormann L. Effects of (-)-hydroxycitric acid on appetitive variables. Physiol Behav. 71(1-2):87-94, 2000. www.elsevier.com.

Thom H. Hydroxycitrate in the treatment of obesity. Int J Obesity. 20:75, 1996. www.nature.com/ijo.

Preuss HG et al. Weight management and mechanism of appetite suppression by a novel, natural extract of ()-hydroxycitric acid. Int Sci Conf Comp Alt Int Med Res. (Harvard Medical School), p. 9, Abs. 141, April 12, 2002. www.interhealthusa.com.

Jena BS et al. Chemistry and biochemistry of (-)-hydroxycitric Acid from garcinia. J Agric Food Chem. 50(1):10-22, 2002. http://pubs.acs.org.

Leonhardt M et al. Effect of hydroxycitrate on food intake and body weight regain after a period of restrictive feeding in male rats. Physiol Behav. 74(1-2):191-6, 2001. www.elsevier.com.

Ahmad F et al. Insulin and glucagon releasing activity of coleonol (forskolin) and its effect on blood glucose level in normal and alloxan diabetic rats. Acta Diabetol Lat. 28(1):71-7, 1991. http://link.springer.de/link/service/journals/00592.

Sabinsa Corporation. Effect of ForsLean on body weight, body fat and lean body mass in overweight subjects. Unpublished. www.forslean.com.

Beckles GLA et al. Population-based assessment of the level of care among adults with diabetes in the U.S. Diabetes Care 21(9):1432-8, 1998. http://care.diabetesjournals.org.

Bishayee A, Chatterjee M. Hypolipidemic and antiatherosclerotic effects of oral Gymnema sylvestre R.Br. leaf extract in albino rats fed on a high fat diet. Phytother Res. 8:118-20, 1994. www.interscience.wiley.com/jpages/0951-418X.

Pathak B et al. Thermic effect of citrus aurantium in obese subjects. U.S. Patent #6,224,873. www.nutratechinc.com.

Colker CM et al. Effects of Citrus aurantium extract, caffeine and St. Johns wort on body fat loss, lipid levels and mood states in overweight healthy adults. Curr Ther Res. 60(3):145-53, 1999. www.currenttherapeuticres.com.

Smedman A, Vessby B. Conjugated linoleic acid supplementation in humans--metabolic effects. Lipids. 36:773-81, 2001. www.aocs.org.

Riserus U et al. Conjugated linoleic acid (CLA) reduced abdominal adipose tissue in obese middle-aged men with signs of the metabolic syndrome: a randomized controlled trial. Int J Obesity. 25(8):1129-35, 2001. www.naturesj.com/ijo.

Thom E et al. Conjugated linoleic acid reduces body fat in healthy exercising humans. J Int Med Res. 29(5):392-96, 2001. www.jimronline.net.

Terpstra AHM et al. The decrease in body fat in mice fed conjugated linoleic acid is due to increases in energy expenditure and 3energy loss in the excreta. J Nutr. 132:940-5, 2002. www.nutrition.org.

Kakuda T et al. Hypoglycemic effect of extracts from Lagerstroemia speciosa L. leaves in genetically diabetic KK-AY mice. Biosci Biotechnol Biochem. 60(2):204-8, 1996. http://wwwsoc.nii.ac.jp/jsbba/index-e.html.

Suzuki Y et al. Antiobesity activity of extracts from Lagerstroemia speciosa L. leaves on female KK-Ay mice. J Nutr Sci Vitaminol (Tokyo). 45(6):791-5, 1999. http://eishoku.bcasj.or.jp/journal-e.html.

Bell SJ, Goodrick GK. A functional food product for the management of weight. Crit Rev Food Sci Nutr. 42(2):163-78, 2002. www4.infotrieve.com.

Crawford V et al. Effects of niacin-bound chromium supplementation on body composition in overweight African-American women. Diabetes Obes Metab. 1(6):331-7, 1999. www.blackwell-synergy.com.

Kaats GR et al. A randomized, double masked, placebo-controlled study of the effects of chromium picolinate supplementation on body composition: a replication and extension of a previous study. Curr Ther Res. 59(6):379-88, 1998. www.currenttherapeuticres.com.

Volpe SL et al. Effect of chromium supplementation and exercise on body composition, resting metabolic rate and selected biochemical parameters in moderately obese women following an exercise program. J Am Coll Nutr. 20(4):293-306, 2001. www.am-coll-nutr.org/jacn/jacn.htm.

Carruth BR, Skinner JD. The role of dietary calcium and other nutrients in moderating body fat in preschool children. Int J Obesity. 25(4):559-66, 2001. www.naturesj.com/ijo.

Rehder D et al. In vitro study of the insulin-mimetic behaviour of vanadium (IV, V) coordination compounds. J Biol Inorg Chem. 7(4-5):384-96, 2002. http://link.springer.de/link/service/journals/00775/index.htm.

Semiz S et al. Effects of diabetes, vanadium and insulin on glycogen synthase activation in Wistar rats. Mol Cell Biochem. 231(1-2):23-35, 2002. www.wkap.nl. 

Vinson et al. White bean extract reduces starch absorption by 66% in pilot study. Unpublished. www.pharmachemlabs.com.

Consorzio RTC et al. Standardized bean extract promotes weight loss in humans. Unpublished. www.pharmachemlabs.com.

Koike D et al. Effect of a wheat amylase inhibitor on canine carbohydrate digestion, gastrointestinal function and pancreatic growth. Gastroenterology. 108(4):1221-9, 1995. www.gastrojournal.org.

Choudhury et al. Character of a wheat amylase inhibitor preparation and effects on fasting human pancreaticobiliary secretions and hormones. Gastroenterology. 111(5):1313-20, 1996. www.gastrojournal.org.

Schiller RN et al. A randomized, double blind, placebo-controlled study examining the effects of a rapidly soluble chitosan dietary supplement on weight loss and body composition in overweight and mildly obese individuals. JANA. 4(1):42-9, 2001. www.americanutra.com/jana.html.

Gades MD, Stern JS. Chitosan supplementation does not affect fat absorption in healthy males fed a high-fat diet, a pilot study. Int J Obes Relat Metab Disord. 26(1):119-22, 2002. www-us.ebsco.com/online/OnlineTitles.asp.

Ho SC et al. In the absence of dietary surveillance, chitosan does not reduce plasma lipids or obesity in hypercholesterolaemic obese Asian subjects. Singapore Med J. 42(1):6-10, 2001. www.sma.org.sg/smj/smjcurrent.html.