Menu
Peptide Database
Results
No peptides found
Featured

Use search to browse all 100+ peptides

Kisspeptin-10

KP-10, Metastin (45-54), Kisspeptin-10 (human), KiSS-1

Quick Stats
Studies 877
Trials 47
Score 2
2016 pubmed 14 citations

Investigation of the effects of kisspeptin-10 in methionine-induced lipid peroxidation in testicle tissue of young rats.

Akkaya. Hatice H; Eyuboglu. Signem S; Erkanlı Senturk. Gozde G; Yilmaz. Bayram B

Key Findings

  • Kisspeptin‑10 raised catalase activity and mRNA levels in testicular tissue under oxidative stress
  • Superoxide dismutase activity and its gene expression also increased with kisspeptin‑10
  • Spermatogenic cell structure was preserved and no obvious harm to sperm cells was seen

Practical Outcomes

  • The results hint that kisspeptin could offer antioxidant protection for male reproductive health, but the evidence is limited to animal models. No human dosing or safety data are available, so it’s not ready for a DIY protocol yet.

Summary

In a rat study, giving kisspeptin‑10 helped boost antioxidant enzymes in the testes and reduced damage caused by a high‑methionine diet, without harming sperm cells. The hormone changes were modest, and the work is only in young rats, not people.

Abstract

Disruption of the balance oxidants, antioxidants cause various pathophysiological conditions such as lipid peroxidation, protein degradation, or DNA damage. We have examined possible effects of kisspeptin-10 on the structural damage produced by methionine-induced lipid peroxidation in testicle tissue of young rats. Kisspeptin-10 did not significantly affect spermatogenic cells in seminiferous tubules. Testosterone levels decreased in the methionine group as compared with the control group but without statistical significance. Luteinizing hormone levels decreased in the methionine group as compared with the control group (P < 0.001). Catalase enzyme activity increased in the kisspeptin-10 group (P < 0.01) as compared with the other groups. Catalase mRNA expression was decreased in the methionine group as compared with the kisspeptin group (P < 0.001). Total superoxide dismutase enzyme activity and superoxide dismutase mRNA expression were increased in the kisspeptin group as compared with the methionine group (P < 0.05). In conclusion, kisspeptin treatment may protect the structure of spermatogenic cells against methionine-induced damage.

Study Information

Provider

pubmed

Year

2016

Date

2016-11-30T00:00:00.000Z

DOI

10.1002/jbt.21881

Citations

14

References

38