Chronic rhein treatment improves recognition memory in high-fat diet-induced obese male mice

J Nutr Biochem. 2016 Oct:36:42-50. doi: 10.1016/j.jnutbio.2016.07.008. Epub 2016 Aug 4.

Abstract

High-fat (HF) diet modulates gut microbiota and increases plasma concentration of lipopolysaccharide (LPS) which is associated with obesity and its related low-grade inflammation and cognitive decline. Rhein is the main ingredient of the rhubarb plant which has been used as an anti-inflammatory agent for several millennia. However, the potential effects of rhein against HF diet-induced obesity and its associated alteration of gut microbiota, inflammation and cognitive decline have not been studied. In this study, C57BL/6J male mice were fed an HF diet for 8 weeks to induce obesity, and then treated with oral rhein (120 mg/kg body weight/day in HF diet) for a further 6 weeks. Chronic rhein treatment prevented the HF diet-induced recognition memory impairment assessed by the novel object recognition test, neuroinflammation and brain-derived neurotrophic factor (BDNF) deficits in the perirhinal cortex. Furthermore, rhein inhibited the HF diet-induced increased plasma LPS level and the proinflammatory macrophage accumulation in the colon and alteration of microbiota, including decreasing Bacteroides-Prevotella spp. and Desulfovibrios spp. DNA and increasing Bifidobacterium spp. and Lactobacillus spp. DNA. Moreover, rhein also reduced body weight and improved glucose tolerance in HF diet-induced obese mice. In conclusion, rhein improved recognition memory and prevented obesity in mice on a chronic HF diet. These beneficial effects occur via the modulation of microbiota, hypoendotoxinemia, inhibition of macrophage accumulation, anti-neuroinflammation and the improvement of BDNF expression. Therefore, supplementation with rhein-enriched food or herbal medicine could be beneficial as a preventive strategy for chronic HF diet-induced cognitive decline, microbiota alteration and neuroinflammation.

Keywords: Gut microbiota; Inflammation; Lipopolysaccharide; Perirhinal cortex; Recognition memory; Rhein.

MeSH terms

  • Animals
  • Anthraquinones / therapeutic use*
  • Anti-Inflammatory Agents, Non-Steroidal / therapeutic use*
  • Anti-Obesity Agents / therapeutic use
  • Brain-Derived Neurotrophic Factor / metabolism
  • Colon / immunology
  • Colon / metabolism
  • Colon / microbiology
  • Colon / pathology
  • Diet, High-Fat / adverse effects
  • Dietary Supplements*
  • Dysbiosis / etiology
  • Dysbiosis / microbiology
  • Dysbiosis / prevention & control*
  • Endotoxemia / etiology
  • Endotoxemia / prevention & control
  • Gastrointestinal Agents / therapeutic use
  • Glucose Intolerance / etiology
  • Glucose Intolerance / prevention & control
  • Intestinal Mucosa / immunology
  • Intestinal Mucosa / metabolism
  • Intestinal Mucosa / microbiology
  • Intestinal Mucosa / pathology
  • Male
  • Memory Disorders / etiology
  • Memory Disorders / prevention & control*
  • Mice, Inbred C57BL
  • Neuritis / etiology
  • Neuritis / prevention & control
  • Neurons / immunology
  • Neurons / metabolism
  • Neurons / pathology
  • Nootropic Agents / therapeutic use*
  • Obesity / diet therapy*
  • Obesity / immunology
  • Obesity / pathology
  • Obesity / physiopathology
  • Perirhinal Cortex / immunology
  • Perirhinal Cortex / metabolism
  • Perirhinal Cortex / pathology
  • Recognition, Psychology

Substances

  • Anthraquinones
  • Anti-Inflammatory Agents, Non-Steroidal
  • Anti-Obesity Agents
  • Brain-Derived Neurotrophic Factor
  • Gastrointestinal Agents
  • Nootropic Agents
  • rhein