Omega-3 polyunsaturated fatty acids alleviate hydrogen sulfide-induced blood-testis barrier disruption in the testes of adult mice

Reprod Toxicol. 2020 Dec:98:233-241. doi: 10.1016/j.reprotox.2020.10.007. Epub 2020 Oct 15.

Abstract

Hydrogen sulfide (H2S), a gaseous intracellular signal transducer, participates in multiple physiological and pathological conditions, including reproductive conditions, and disrupts spermatogenesis. The blood-testis barrier (BTB) plays a vital role in spermatogenesis. However, the effect of H2S on the BTB and the underlying mechanism remain unclear. Herein, we examined the effect of H2S and omega-3 polyunsaturated fatty acids (ω-3 PUFAs) on the BTB and testicular functions. ICR male mice were randomly divided into the following groups: control, H2S exposure, and H2S exposure with ω-3 PUFAs intervention. The sperm parameters (sperm concentration and sperm motility) declined in the H2S group and improved in the ω-3 intervention group. BTB integrity was severely disrupted by H2S, and the BTB-related gene levels (ZO-1, Occludin, Claudin 11) decreased; ω-3 supplementation could alleviate BTB disruption by upregulating BTB-related genes, and TM4 Sertoli cells had a similar trend in vitro. p38 MAPK phosphorylation was upregulated in the Na2S treatment group and downregulated after ω-3 cotreatment. These findings suggest that H2S can impair the BTB and that ω-3 PUFAs supplementation can attenuate H2S toxicity in the male reproductive system. Our study elucidated the relationship between a gasotransmitter (H2S) and the BTB and identified the potential therapeutic effect of ω-3 PUFAs.

Keywords: Sertoli cell; blood-testis barrier; hydrogen sulfide; omega-3 PUFAs; p38.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blood-Testis Barrier / drug effects*
  • Blood-Testis Barrier / metabolism
  • Cell Line
  • Fatty Acids, Omega-3 / pharmacology*
  • Gene Expression Regulation / drug effects
  • Male
  • Mice, Inbred ICR
  • Sperm Count
  • Sperm Motility / drug effects
  • Spermatozoa / drug effects
  • Sulfides / toxicity*
  • Testosterone / blood
  • Tight Junction Proteins / genetics
  • p38 Mitogen-Activated Protein Kinases / metabolism

Substances

  • Fatty Acids, Omega-3
  • Sulfides
  • Tight Junction Proteins
  • Testosterone
  • p38 Mitogen-Activated Protein Kinases
  • sodium sulfide