Gastroprotective and Healing Effects of Polygonum cuspidatum Root on Experimentally Induced Gastric Ulcers in Rats

Nutrients. 2020 Jul 27;12(8):2241. doi: 10.3390/nu12082241.

Abstract

Polygonum cuspidatum is widely used as food and medicine in Korea, China, and Japan. Its major bioactive components, resveratrol and emodin, reportedly protect against gastric lesions. We therefore aimed to investigate: (1) the gastroprotective effects of P. cuspidatum roots in hydrochloric acid/ethanol (HCl/EtOH)- and indomethacin-induced acute gastric ulcer rat models; (2) the healing effects in an acetic acid-induced ulcer model; and (3) potential mechanisms by measuring gastric acid secretion-related parameters in a pyloric ligation-induced ulcer model, and by measuring antioxidant enzyme and prostaglandin E2 levels in the gastric tissue of HCl/EtOH-treated rats. Oral administration of P. cuspidatum extract (PCE) at doses of 100 and 300 mg/kg significantly decreased HCl/EtOH- and indomethacin-induced gastric lesions. PCE at 300 mg/kg significantly reduced gastric lesions in acetic acid-induced ulcers. PCE increased superoxide dismutase (SOD)activity and glutathione(GSH) and prostaglandin E2 levels in gastric tissue, whereas it did not alter gastric acid secretion-related parameters. Our findings indicate that PCE has gastroprotective effects against HCl/EtOH and non-steroidal anti-inflammatory drugs(NSAIDs) and promotes healing of acetic acid-induced ulcers. These gastric mucosal protection and ulcer healing effects are associated with antioxidant effects and the augmentation of prostaglandin E2 and suggest that P. cuspidatum might be a promising preventive and therapeutic agent for treating gastric ulcers.

Keywords: Polygonum cuspidatum; antioxidant; gastric acid; gastric ulcer; gastritis; prostaglandin E2.

MeSH terms

  • Acetic Acid
  • Animals
  • Anti-Inflammatory Agents, Non-Steroidal / adverse effects
  • Antioxidants / metabolism
  • Dinoprostone / metabolism
  • Disease Models, Animal
  • Ethanol
  • Fallopia japonica*
  • Gastric Mucosa / metabolism
  • Gastrointestinal Agents / pharmacology*
  • Hydrochloric Acid
  • Indomethacin
  • Male
  • Plant Extracts / pharmacology*
  • Plant Roots*
  • Protective Agents / pharmacology*
  • Rats
  • Rats, Sprague-Dawley
  • Stomach Ulcer / chemically induced
  • Stomach Ulcer / therapy*

Substances

  • Anti-Inflammatory Agents, Non-Steroidal
  • Antioxidants
  • Gastrointestinal Agents
  • Plant Extracts
  • Protective Agents
  • Ethanol
  • Dinoprostone
  • Acetic Acid
  • Hydrochloric Acid
  • Indomethacin