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Humanin

HN, S14G-Humanin

Quick Stats
Studies 491
Trials 100
Score 4
2019 pubmed 17 citations

Potent humanin analogue (HNG) protects human sperm from freeze-thaw-induced damage.

Yang. Chao C; Xu. Ling L; Cui. Yingdong Y; Wu. Bo B; Liao. Zhaolin Z

Key Findings

  • HNG at 2‑10 µM improves sperm motility and viability after freeze‑thaw
  • HNG reduces mitochondrial damage, DNA fragmentation, oxidative stress, and caspase‑3 activity in frozen sperm
  • Increasing HNG to 20 µM does not further improve outcomes over 10 µM

Practical Outcomes

  • If you freeze your own sperm or work with cryopreserved samples, adding HNG at ~10 µM to the freezing medium could boost survival and quality. This dosage is a practical target and higher amounts aren’t needed, making it a simple protocol tweak for better fertility preservation.

Summary

Adding the humanin analogue HNG to the liquid used when freezing sperm helps keep the cells alive and working better after they’re thawed. The best effect was seen at a medium dose (about 10 micromolar), with higher doses not giving extra benefit.

Abstract

This study was aimed to investigate the protective effect of potent humanin analogue (HNG) supplementation to freezing media on freezing-thawing induced human sperm damage. We collected semen samples with normal sperm parameters from 15 healthy men. After the swim-up processing, the motile spermatozoa from each of the men were allocated to four equal groups: In the control group, the spermatozoa were frozen in media without HNG supplementation. In the other three groups, the spermatozoa were frozen in media supplemented with different concentrations of HNG (2 μM, 10 μM and 20 μM, respectively). We analyzed the sperm motility, viability, sperm mitochondrial membrane potential, apoptosis, sperm DNA fragmentation index (DFI), reactive oxygen species (ROS) and malondialdehyde (MDA) levels, and caspase-3 activity for the sperm in each group. As a result, supplementation of HNG with 2 μM, 10 μM and 20 μM to the freezing media all significantly improved sperm motility and viability (all p < 0.05) when compared with the control group. Similarly, we found that supplementation of HNG reduced the damage to the mitochondrial membrane and DNA integrity, and inhibited the reaction of oxidative stress and the activity of caspase-3 in sperm. Although these protective effects increased with the elevated concentration of HNG in the freezing media, a final HNG concentration of 20 μM failed to exert significant improvements when compared with the concentration of 10 μM (all p > 0.05). In conclusion, our results suggested that HNG supplementation to the freezing media could protect sperm cells from freezing-thawing induced sperm damage.

Study Information

Provider

pubmed

Year

2019

Date

2019-04-06T00:00:00.000Z

DOI

10.1016/j.cryobiol.2019.04.001

Citations

17

References

42