pregna-4-17-diene-3-16-dione has been researched along with Obesity* in 3 studies
1 review(s) available for pregna-4-17-diene-3-16-dione and Obesity
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Guggulipid: A Promising Multi-Purpose Herbal Medicinal Agent.
Herbal medicines therapy is appreciated by many research works because herbal drugs have relatively high therapeutic window, lower side effects and more cost effective. Guggulipid is an ethyl acetate extract of resin known as guggul from the tree Topics: Acne Vulgaris; Arthritis; Commiphora; Epilepsy; Humans; Inflammation; Lipid Metabolism Disorders; Liver Diseases; Obesity; Pain; Peptic Ulcer; Plant Extracts; Plant Gums; Pregnenediones; Stereoisomerism | 2020 |
2 other study(ies) available for pregna-4-17-diene-3-16-dione and Obesity
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The appetite regulatory effect of guggulsterones in rats: a repertoire of plasma hormones and neurotransmitters.
Guggulsterone or guggulipid is a steroidal constituent present in the neutral fraction of gum resin of Commiphora mukul, commonly known as guggul. The traditional uses of guggul-resin extract are well documented in the Ayurveda-where it is prescribed to treat a variety of ailments including lipid-related disorders such as obesity and arteriosclerosis. The hypolipidemic activity of the extracts known since ancient times can be traced to the two closely related steroidal ketones, E-guggulsterone and Z-guggulsterone. In this study, we have investigated the dose dependent (100, 200, 400 mg/kg body weight) effect of guggulsterones on appetite regulating hormones [ghrelin, leptin, cholecystokinin (CCK)] and neurotransmitters (serotonin and dopamine), which play a major role in the energy homeostasis and thus influence obesity related factors. We have also studied its effect on food intake, body weight and plasma triglycerides and glucose in rats. Guggulsterones at the dose of 400 mg/kg body weight was able to significantly reduce food intake and limit body weight gain over a period of 15 days. It also significantly decreased the plasma ghrelin, glucose, triglyceride levels and increased plasma leptin, serotonin, dopamine levels, but did not show much effect on CCK levels. Topics: Animals; Appetite; Blood Glucose; Cholecystokinin; Commiphora; Dopamine; Dose-Response Relationship, Drug; Eating; Energy Intake; Ghrelin; Leptin; Male; Obesity; Plant Extracts; Plant Gums; Pregnenediones; Rats, Wistar; Resins, Plant; Serotonin; Triglycerides; Weight Gain | 2014 |
Anti-obesity effects of xanthohumol plus guggulsterone in 3T3-L1 adipocytes.
Xanthohumol (XN) and guggulsterone (GS) have each been shown to inhibit adipogenesis and induce apoptosis in adipocytes. In the present study effects of the combination of XN + GS on 3T3-L1 adipocyte apoptosis and adipogenesis were investigated. Mature adipocytes were treated with XN and GS individually and in combination. XN and GS individually decreased cell viability, but XN + GS caused an enhanced decrease in viability and potentiated induction of apoptosis. Likewise, XN + GS caused a potentiated increase in caspase-3/7 activation, whereas neither of the compounds showed any effect individually. In addition, western blot analysis revealed that XN + GS increased Bax expression and decreased Bcl-2 expression, whereas individual compounds did not show any significant effect. XN and GS both decreased lipid accumulation. Individually, XN at 1.5 microM and GS at 3.12 microM decreased lipid accumulation by 26 +/- 4.5% (P < .001) each, whereas XN1.5 + GS3.12 decreased lipid accumulation by 78.2 +/- 1.8% (P < .001). Moreover, expression of the adipocyte-specific proteins was down-regulated with XN1.5 + GS3.12, but no effect was observed with the individual compounds. Finally, XN + GS caused an enhanced stimulation of lipolysis. Thus, combination of XN and GS is more potent in exerting anti-obesity effects than additive effects of the individual compounds. Topics: 3T3-L1 Cells; Adipocytes; Adipogenesis; Animals; Anti-Obesity Agents; Apoptosis; bcl-2-Associated X Protein; Caspases; Cell Survival; Commiphora; Down-Regulation; Drug Therapy, Combination; Flavonoids; Gene Expression; Lipid Metabolism; Lipolysis; Mice; Obesity; Phytotherapy; Plant Extracts; Pregnenediones; Propiophenones; Proto-Oncogene Proteins c-bcl-2 | 2009 |