Antidiarrheal effects of water-soluble proteins from Plumeria pudica latex in mice

Biomed Pharmacother. 2018 Jan:97:1147-1154. doi: 10.1016/j.biopha.2017.11.019. Epub 2017 Nov 11.

Abstract

The water-soluble protein fraction obtained from Plumeria pudica (LPPp) latex has previously been demonstrated to have anti-inflammatory and antinociceptive effects. In the present study, LPPp was tested for activity against diarrhea induced by castor oil, prostaglandin E2 (PGE2) or cholera toxin. Different doses of LPPp (10, 20 or 40mg/kg) significantly inhibited the percentage of diarrheal stools (31.18%, 42.97% and 59.70%, respectively) induced by castor oil. This event was followed by significant reduction of both intestinal fluid accumulation (31.42%; LPPp 40mg/kg) and intestinal transit (68.4%; LPPp 40mg/kg). The pretreatment of animals with LPPp (40mg/kg) prevented glutathione and malondialdehyde alterations induced by castor oil. The effects of LPPp against diarrhea induced by castor oil were lost when the fraction was submitted to protein denaturing treatment with heat. LPPp (40mg/kg) also inhibited the average volume of intestinal fluid induced by PGE2 (inhibition of 46.0%). Furthermore, LPPp (40mg/kg) prevented intestinal fluid secretion accumulation (37.7%) and chloride ion concentration (50.2%) induced by cholera toxin. In parallel, colorimetric assays demonstrated that proteinases, chitinases and proteinase inhibitors were found in LPPp. Our data suggest that the antidiarrheal effect of LPPp is due to its protein content and is probably associated with its anti-inflammatory properties.

Keywords: Castor oil; Chitinases; Cholera; PGE(2); Proteinase; Proteinase inhibitor.

MeSH terms

  • Animals
  • Anti-Inflammatory Agents / administration & dosage
  • Anti-Inflammatory Agents / isolation & purification
  • Anti-Inflammatory Agents / pharmacology
  • Antidiarrheals / administration & dosage
  • Antidiarrheals / isolation & purification
  • Antidiarrheals / pharmacology*
  • Apocynaceae / chemistry*
  • Diarrhea / drug therapy*
  • Disease Models, Animal
  • Dose-Response Relationship, Drug
  • Glutathione / metabolism
  • Intestinal Mucosa / metabolism
  • Intestines / drug effects
  • Male
  • Malondialdehyde / metabolism
  • Mice
  • Plant Extracts / administration & dosage
  • Plant Extracts / pharmacology*
  • Plant Proteins / administration & dosage
  • Plant Proteins / isolation & purification
  • Plant Proteins / pharmacology*
  • Solubility
  • Water / chemistry

Substances

  • Anti-Inflammatory Agents
  • Antidiarrheals
  • Plant Extracts
  • Plant Proteins
  • Water
  • Malondialdehyde
  • Glutathione