The potential of artemisinins as anti-obesity agents via modulating the immune system

Pharmacol Ther. 2020 Dec:216:107696. doi: 10.1016/j.pharmthera.2020.107696. Epub 2020 Oct 3.

Abstract

Artemisinin and its derivatives are the most effective antimalarial drugs. Besides anti-malarial activity, artemisinin and its derivatives have displayed wide-spectrum bioactivities such as anti-parasite, anti-tumor, and anti-obesity effects. Obesity is an epidemic worldwide which is a big threat to human health, but there are only a few approved anti-obesity drugs in the world. Also, these drugs are efficient to limited patients partly because their safety and efficacy are questioned. Anti-inflammatory therapies may be valuable in obesity treatment since growing evidence shows chronic metabolic inflammation is implicated in metabolic disease pathogenesis. As artemisinin and its derivatives display effective anti-inflammatory and immunoregulatory properties with less toxicity, it provides an insight for novel drug development in obesity therapeutic strategies via immune-regulatory mechanisms. In this review, the potential of artemisinin and its derivatives to treat various metabolic diseases such as obesity and diabetes is discussed.

Keywords: Anti-inflammatory; Artemisinin; Diabetes; Drug development; Multi-target; Obesity.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Anti-Inflammatory Agents / adverse effects
  • Anti-Inflammatory Agents / chemistry
  • Anti-Inflammatory Agents / therapeutic use*
  • Anti-Obesity Agents / adverse effects
  • Anti-Obesity Agents / chemistry
  • Anti-Obesity Agents / therapeutic use*
  • Artemisinins / adverse effects
  • Artemisinins / chemistry
  • Artemisinins / therapeutic use*
  • Endoplasmic Reticulum Stress / drug effects
  • Energy Metabolism / drug effects
  • Humans
  • Immune System / drug effects*
  • Immune System / immunology
  • Immune System / metabolism
  • Immune System / physiopathology
  • Inflammation Mediators / metabolism
  • Insulin Resistance
  • Molecular Structure
  • Obesity / drug therapy*
  • Obesity / immunology
  • Obesity / metabolism
  • Obesity / physiopathology
  • Signal Transduction
  • Structure-Activity Relationship

Substances

  • Anti-Inflammatory Agents
  • Anti-Obesity Agents
  • Artemisinins
  • Inflammation Mediators