Enhanced expression of cystathionine β-synthase and cystathionine γ-lyase during acute cholecystitis-induced gallbladder inflammation

PLoS One. 2013 Dec 9;8(12):e82711. doi: 10.1371/journal.pone.0082711. eCollection 2013.

Abstract

Background: Hydrogen sulfide (H2S) has recently been shown to play an important role in the digestive system, but the role of endogenous H2S produced locally in the gallbladder is unknown. The aim of this study was to investigate whether gallbladder possesses the enzymatic machinery to synthesize H2S, and whether H2S synthesis is changed in gallbladder inflammation during acute acalculous cholecystitis (AC).

Methods: Adult male guinea pigs underwent either a sham operation or common bile duct ligation (CBDL). One, two, or three days after CBDL, the animals were sacrificed separately. Hematoxylin and eosin-stained slides of gallbladder samples were scored for inflammation. H2S production rate in gallbladder tissue from each group was determined; immunohistochemistry and western blotting were used to determine expression levels of the H2S-producing enzymes cystathionine β-synthase (CBS) and cystathionine γ-lyase (CSE) in gallbladder.

Results: There was a progressive inflammatory response after CBDL. Immunohistochemistry analysis showed that CBS and CSE were expressed in the gallbladder epithelium, muscular layer, and blood vessels and that the expression increased progressively with increasing inflammation following CBDL. The expression of CBS protein as well as the H2S-production rate was significantly increased in the animals that underwent CBDL, compared to those that underwent the sham operation.

Conclusions: Both CBS and CSE are expressed in gallbladder tissues. The expression of these enzymes, as well as H2S synthesis, was up-regulated in the context of inflammation during AC.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cholecystitis, Acute / etiology
  • Cholecystitis, Acute / metabolism*
  • Cholecystitis, Acute / pathology
  • Common Bile Duct / surgery
  • Cystathionine beta-Synthase / metabolism*
  • Cystathionine gamma-Lyase / metabolism*
  • Disease Models, Animal
  • Gallbladder / metabolism
  • Gallbladder / pathology
  • Guinea Pigs
  • Histocytochemistry
  • Immunohistochemistry
  • Ligation
  • Male
  • Mucous Membrane / metabolism
  • Mucous Membrane / pathology
  • Sulfites / metabolism

Substances

  • Sulfites
  • Cystathionine beta-Synthase
  • Cystathionine gamma-Lyase
  • hydrogen sulfite

Grants and funding

This work was supported by National Natural Science Foundation of China (No. 81170351) and the Fundamental Research Funds for the Central Universities (No.2012302020213). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.