Oral supplementation with ginseng polysaccharide promotes food intake in mice

Brain Behav. 2019 Sep;9(9):e01340. doi: 10.1002/brb3.1340. Epub 2019 Aug 8.

Abstract

Introduction: Ginseng polysaccharide (GPS, same as Panax polysaccharide) is a kind of polysaccharide extracted from ginseng. It has been reported that GPS has the ability to activate innate immunity, regulates blood sugar balance, and improves antioxidant capacity, but the effect on feeding behavior and its mechanism remains unclear.

Method: To investigate the possible effect of GPS on feeding behavior of animals, mice were supplied with GPS in water, and food intake, hedonic feeding behavior, anxiety-like behavior, expression of appetite-regulation peptides in the central nervous system and glucose-related hormone levels in the serum of mice were measured.

Results: Ginseng polysaccharide significantly increased the average daily food intake in mice and promoted hedonic eating behavior. Meanwhile, the levels of serum glucose and glucagon were significantly reduced by GPS, and GPS promoted hypothalamic neuropeptide Y expression, inhibited proopiomelanocortin (POMC) expression, and reduced dopamine D1 receptor (DRD1) levels in the midbrain. We also found that the anxiety level of mice was significantly lower after GPS intake. In conclusion, oral supplementation with GPS promoted food intake in mice, most likely through the regulation of circulating glucose levels.

Keywords: blood glucose; feeding behavior; hypothalamus; panax; polysaccharides.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Anxiety
  • Behavior, Animal / drug effects
  • Blood Glucose / drug effects
  • Blood Glucose / metabolism
  • Dietary Supplements
  • Dopamine Plasma Membrane Transport Proteins / drug effects
  • Dopamine Plasma Membrane Transport Proteins / genetics
  • Eating / drug effects
  • Feeding Behavior / drug effects*
  • Glucagon / drug effects
  • Glucagon / metabolism
  • Hypothalamus / drug effects
  • Hypothalamus / metabolism
  • Insulin / metabolism
  • Male
  • Mesencephalon / drug effects
  • Mesencephalon / metabolism
  • Mice
  • Neuropeptide Y / drug effects
  • Neuropeptide Y / metabolism
  • Panax*
  • Polysaccharides / pharmacology*
  • Pro-Opiomelanocortin / drug effects
  • Pro-Opiomelanocortin / metabolism
  • RNA, Messenger / drug effects
  • RNA, Messenger / metabolism
  • Receptors, Dopamine D1 / drug effects
  • Receptors, Dopamine D1 / genetics
  • Receptors, Dopamine D2 / drug effects
  • Receptors, Dopamine D2 / genetics

Substances

  • Blood Glucose
  • DRD2 protein, mouse
  • Dopamine Plasma Membrane Transport Proteins
  • Drd1 protein, mouse
  • Insulin
  • Neuropeptide Y
  • Polysaccharides
  • RNA, Messenger
  • Receptors, Dopamine D1
  • Receptors, Dopamine D2
  • Pro-Opiomelanocortin
  • Glucagon