Advanced search×

Studies on the metabolism and toxicology of emerging capsinoids.

Expert Opin Drug Metab Toxicol 7(5):533-42 (2011) PMID 21355789

INTRODUCTION: Capsinoids are nonpungent compounds that are found in almost all pungent peppers and are abundant in the sweet pepper cultivar CH-19 Sweet. Since the discovery of capsinoids 13 years ago, various physiological effects of these compounds - especially reduction of visceral fat - have been observed both in rodents and humans. Recently, capsules containing capsinoids have become commercially available and comprehensive studies have been performed on the metabolism and toxicity of capsinoids. AREAS COVERED: This article reviews all the literature from 1998 to date providing details on the nature and physiological effects of capsinoids. In addition to this, the article also looks at their metabolism as well as their acute and chronic toxicity including their genotoxicity and teratology. EXPERT OPINION: Capsinoids are the most promising compounds among all known transient receptor potential vanilloid 1 agonists. The physiological activities of capsinoids are similar to those of capsaicin, the most pungent food component of red pepper, but appear to be much safer to use as a therapeutic compound. That said, there is still a need for further research into the capsinoid mechanism of action before it can be 'green-lighted' for therapeutic use.

Version: za2963e q8zaf q8zb5 q8zc1 q8zd2 q8ze1 q8zf6 q8zgd

Similar articles you may find interesting…

  1. UDP-glucuronosyltransferase 2B15 (UGT2B15) is the Major Enzyme Responsible for Sipoglitazar Glucuronidation in Humans: Retrospective Identif...

    Drug Metab Pharmacokinet (2013) PMID 23648677

    These results show that sipoglitazar is a good example to elucidate the relationship between phenotype and genotype for UGT2B15 from in vitro analysis....
  2. The many facets of PEDF in drug discovery and disease: a diamond in the rough or split personality disorder?

    Expert Opin Drug Discov (2013) PMID 23642051

    Pigment epithelium-derived factor (PEDF) was discovered as a neurotrophic factor secreted by retinal pigment epithelial cells. A decade later, it re-emerged as a powerful angiogenesis inhibitor guarding ocular function. Since then, significant advances were made identifying PEDF's mechanisms, target...
  3. Frequency of the functionally relevant aryl hydrocarbon receptor repressor (AhRR) Pro185Ala SNP in Papua New Guinea.

    Drug Metab Pharmacokinet (2013) PMID 23648678

    We can hypothesize that a high frequency of the AhRR SNP can be a risk factor in the incidence of oral cancer and other neoplasias in PNG due to higher inducibility of CYP1A2. The potential role of AhRR pharmacogenetics in the risk of developing cancers associated with betel quid chewing and smoking...