The efficacy of a sulphated polysaccharide fraction from Hypnea musciformis against diarrhea in rodents

Int J Biol Macromol. 2016 May:86:865-75. doi: 10.1016/j.ijbiomac.2016.02.028. Epub 2016 Feb 12.

Abstract

Seaweeds are sources of diverse bioactive compounds, such as sulphated polysaccharides. This study was designed to evaluate the chemical composition and anti-diarrheal activity of a fraction of sulphated polysaccharide (PLS) obtained from the red seaweed Hypnea musciformis in different animal models, and to elucidate the underlying mechanisms. PLS was obtained by aqueous extraction, with a yield of 31.8% of the seaweed dry weight. The total carbohydrate content accounted for 99% of the sample. The sulfate content of the polysaccharide was 5.08% and the percentage of carbon was 25.98%. Pretreatment with all doses of PLS inhibited castor oil-induced diarrhea, with reduction of the total amount of stool, diarrheal stools, and the severity of diarrhea. PLS (90 mg/Kg) decreased castor oil- and PGE2-induced enteropooling. In addition, PLS (90 mg/Kg) increased the Na(+)/K(+)-ATPase activity in the small intestine and reduced gastrointestinal transit, possibly via activation of cholinergic receptors. Interestingly, the cholera toxin-induced fluid secretion and Cl(-) ion levels decreased in the intestinal contents of the animals pretreated with PLS (90 mg/kg), probably via reduction of toxin-GM1 receptor binding. In conclusion, PLS exerts anti-diarrheal activity by increasing Na(+)/K(+)-ATPase activity, inhibiting gastrointestinal motility, and blocking the toxin-GM1 receptor binding.

Keywords: Algae; Cholera; Sulfated polysaccharide.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Castor Oil / adverse effects
  • Cholera Toxin / toxicity
  • Diarrhea / chemically induced
  • Diarrhea / drug therapy*
  • Diarrhea / metabolism
  • Diarrhea / physiopathology
  • Female
  • Gastrointestinal Transit / drug effects
  • Intestinal Absorption / drug effects
  • Intestine, Small / drug effects
  • Intestine, Small / metabolism
  • Intestine, Small / physiopathology
  • Male
  • Mice
  • Narcotic Antagonists / pharmacology
  • Polysaccharides / chemistry*
  • Polysaccharides / pharmacology*
  • Polysaccharides / therapeutic use
  • Rats
  • Receptors, Cell Surface / metabolism
  • Rhodophyta / chemistry*
  • Sodium-Potassium-Exchanging ATPase / metabolism
  • Sulfates / chemistry*

Substances

  • Narcotic Antagonists
  • Polysaccharides
  • Receptors, Cell Surface
  • Sulfates
  • ganglioside receptor
  • Castor Oil
  • Cholera Toxin
  • Sodium-Potassium-Exchanging ATPase