| Literature DB >> 31680350 |
Xiaoxv Dong1, Yawen Zeng1, Yi Liu1, Longtai You1, Xingbin Yin1, Jing Fu2, Jian Ni3.
Abstract
Aloe-emodin is a naturally anthraquinone derivative and an active ingredient of Chinese herbs, such as Cassia occidentalis, Rheum palmatum L., Aloe vera, and Polygonum multiflorum Thunb. Emerging evidence suggests that aloe-emodin exhibits many pharmacological effects, including anticancer, antivirus, anti-inflammatory, antibacterial, antiparasitic, neuroprotective, and hepatoprotective activities. These pharmacological properties lay the foundation for the treatment of various diseases, including influenza virus, inflammation, sepsis, Alzheimer's disease, glaucoma, malaria, liver fibrosis, psoriasis, Type 2 diabetes, growth disorders, and several types of cancers. However, an increasing number of published studies have reported adverse effects of aloe-emodin. The primary toxicity among these reports is hepatotoxicity and nephrotoxicity, which are of wide concern worldwide. Pharmacokinetic studies have demonstrated that aloe-emodin has a poor intestinal absorption, short elimination half-life, and low bioavailability. This review aims to provide a comprehensive summary of the pharmacology, toxicity, and pharmacokinetics of aloe-emodin reported to date with an emphasis on its biological properties and mechanisms of action.Entities:
Keywords: aloe-emodin; mechanisms; pharmacokinetics; pharmacology; toxicology
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Year: 2019 PMID: 31680350 DOI: 10.1002/ptr.6532
Source DB: PubMed Journal: Phytother Res ISSN: 0951-418X Impact factor: 5.878