1. The present study examined the efficacy of Chlorophytum borivilianum root (powder) in modulating the hyperlipaemic/hypercholesteraemic conditions in male albino rats. 2. Administration of C. borivilianum (0.75 and 1.5 g root powder/rat per day for 4 weeks) to hypercholesteraemic rats significantly increased high-density lipoprotein-cholesterol levels and decreased plasma and hepatic lipid profiles. 3. In addition, there were significant increases in faecal cholesterol, neutral sterol and bile acid excretion with elevated hepatic 3-hydroxy-3-methylglutaryl coenzyme A reductase activity and bile acid production. 4. Furthermore, the hypercholesteraemic rats treated with both doses of C. borivilianum also exhibited increases in superoxide dismutase and ascorbic acid levels. 5. Normocholesteraemic animals treated with both doses of C. borivilianum root powder did not show any significant variation in either lipid or anti-oxidant profiles, except for an increase in the hepatic ascorbic acid concentration compared with their untreated counterparts. 6. The hypolipaemic/hypocholesteraemic effect of C. borivilianum root powder appears to be mediated by an increase in cholesterol turnover via increased faecal cholesterol excretion and, second, through an endogenous cholesterol conversion into bile acid. 7. Administration of C. borivilianum root powder also increased the activities of anti-oxidant enzymes and vitamin C levels, which may have enhanced the anti-oxidant capacity of the liver.
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http://dx.doi.org/10.1111/j.1440-1681.2007.04579.x | DOI Listing |
J Ethnopharmacol
January 2024
Department of Physiology, Faculty of Medicine, University Malaya, 50603, Kuala Lumpur, Malaysia; Centre for Natural Products and Drug Discovery (CENAR), Faculty of Science, University Malaya, 50603, Kuala Lumpur, Malaysia. Electronic address:
Ethnopharmacological Relevance: Chlorophytum borivilianum (C. borivilianum) (CB) has traditionally been used to treat male sexual dysfunctions and has been claimed to possess aphrodisiac properties.
Aim Of The Study: To investigate the ability of CB to ameliorate HO-induced oxidative stress in testes and sperm in mice and prevent HO-induced oxidative in human sperm.
Front Cell Dev Biol
March 2023
Department of Zoology, University of Rajasthan, Jaipur, India.
L. is a recognized herbal medicine for the management of impotency in South Asian countries. In , it is used for the management of multiple health conditions, including diabetes, infection, and cardiovascular diseases.
View Article and Find Full Text PDFPlant Cell Rep
May 2023
Department of Biotechnology, BMS Block I, Panjab University, Sector 25, Chandigarh, 160014, India.
CbSE overexpression increased stigmasterol levels and altered plant morphology. The genes upstream and downstream of CbSE were found to be upregulated, which confirms its regulatory role in the saponin biosynthetic pathway. Chlorophytum borivilianum is a high-value medicinal plant with many promising preclinical applications that include saponins as a major active ingredient.
View Article and Find Full Text PDFFront Pharmacol
January 2022
Department of Zoology, University of Rajasthan, Jaipur, India.
Oxidative stress induced by radiation causes variable expression of antioxidant enzymes in a tissue-specific manner. Testicular tissues carry out the complex process of spermatogenesis, and studies indicate that testicular damages due to irradiation require long-term recovery before complete resumption. Ionizing radiation also causes oxidative stress in tissues, leading to testicular damage.
View Article and Find Full Text PDFIndian J Pharmacol
January 2020
Department of Pharmacology and Therapeutics, Seth G S Medical College and KEM Hospital, Mumbai, Maharashtra, India.
Objectives: The objective was to study the adaptogenic effect of (CB) on physical performance when exposed to accustomed activity (AA) and unaccustomed activity (UA) and the effect of CB on heart rate (HR) and blood pressure (BP) in the presence of UA and the effect on muscle strength in comparison with placebo.
Materials And Methods: A placebo-controlled, double-blind clinical study was initiated after ethics committee approval in healthy volunteers with fixed-dose regimen. Consented volunteers ( = 60) were assigned randomly into two groups of study drug (3 g/day) or placebo (3 g/day) for 2 months.
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