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Humanin

HN, S14G-Humanin

Quick Stats
Studies 491
Trials 100
Score 2
2021 pubmed 8 citations

The role of humanin in the regulation of reproduction.

Lei. Hui H; Rao. Meng M

Key Findings

  • Humanin reduces oxidative stress and apoptosis in ovaries and testes
  • It works by influencing several cell‑signaling pathways
  • Researchers see potential for humanin‑based therapies for infertility, contraception, and PCOS‑related glucose issues

Practical Outcomes

  • At this stage humanin is still a research target, not a supplement you can dose. Keep an eye on future studies for possible humanin‑based products, but there’s no actionable protocol to try today.

Summary

Humanin is a tiny protein made by mitochondria that seems to protect male and female reproductive cells from damage caused by stress and cell death. The paper says it could one day be used to help with infertility, birth control, or conditions like PCOS, but it doesn’t give any concrete ways to use it now.

Abstract

Humanin, a mitochondria-derived peptide, has been found to exert variously protective function in many tissues, especially in the nervous tissues. However, relatively limited studies have focused on the role of humanin in the regulation of reproduction. Current observations indicate that humanin plays an important role in regulating the response of the cell to oxidative stress and apoptosis in ovaries and testes via the modulation of several signaling pathways, especially when the body is in an abnormal state. Even so, the detailed mechanism of humanin function needs to be explored urgently. In this passage, we demonstrate how humanin exerts its protective role in female and male reproduction and raise several questions that need further investigations. Given humanin's new frontier for the design of novel therapeutic approaches for male infertility, male contraception, female infertility, and glucose metabolism in polycystic ovary syndrome, it is worthy of further study on its protective effects and clinical applications in reproductive function.

Study Information

Provider

pubmed

Year

2021

Date

2021-10-07T00:00:00.000Z

DOI

10.1016/j.bbagen.2021.130023

Citations

8

References

39