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Kisspeptin-10

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

Quick Stats
Studies 877
Trials 47
2023 pubmed 7 citations

Role of kisspeptin-10 and betacellulin in control of feline ovarian cell functions.

Loncová. Barbora B; Fabová. Zuzana Z; Sirotkin. Alexander V AV

Key Findings

  • Kisspeptin-10 increased cell proliferation, apoptosis, and release of progesterone and estradiol, while lowering testosterone in feline ovarian cells.
  • Betacellulin decreased proliferation, apoptosis, and all measured hormone releases, and it counteracted the stimulatory actions of kisspeptin-10.
  • Neither protein affected overall cell viability in the short‑term culture.

Practical Outcomes

  • For self‑directed health optimizers, this work offers no immediate, actionable guidance because it is limited to cat ovarian cells and does not provide human dosage or safety data. The findings are primarily of basic scientific interest and do not translate into protocols for longevity, metabolic health, or performance.

Summary

The study looked at how two proteins, kisspeptin-10 and betacellulin, affect ovarian cells taken from cats. Kisspeptin-10 made the cells grow more, die more, and release more female hormones, while betacellulin did the opposite and also blocked kisspeptin's effects. The research was done in a lab setting on cat tissue, not on people.

Abstract

The action of betacellulin (BTC) on basic ovarian cell functions and interrelationships with kisspeptin (KISS) was investigated. For this purpose, we examined (1) the effect of the addition of BTC (0, 1, 10, and 100 ng/ml) given alone or in combination with KISS (10 ng/ml) on cultured feline ovarian fragments or granulosa cells. Viability, proliferation (accumulation of cyclin B1) and apoptosis (accumulation of bax), and the release of steroid hormones (progesterone, testosterone, and estradiol) were analyzed by using the Trypan blue exclusion test, quantitative immunocytochemistry, and ELISA. The addition of KISS alone increased proliferation, apoptosis, progesterone, estradiol release, and decreased testosterone but did not affect viability. The addition of BTC alone decreased cell proliferation, apoptosis, progesterone, testosterone, and estradiol release but did not influence viability. Furthermore, BTC mainly inhibited the stimulatory action of KISS on feline ovarian functions. The findings of our study suggest the effects of KISS on basic ovarian functions. We also observed the influence of BTC on these functions and its ability to modify the effects of KISS on these processes.

Study Information

Provider

pubmed

Year

2023

Date

2023-04-12T00:00:00.000Z

DOI

10.1016/j.repbio.2023.100762

Citations

7

References

29