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Kisspeptin-10

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

Quick Stats
Studies 877
Trials 47
Score 2
2017 pubmed 40 citations

Kisspeptin-10 inhibits proliferation and regulates lipolysis and lipogenesis processes in 3T3-L1 cells and isolated rat adipocytes.

Pruszyńska-Oszmałek. Ewa E; Kołodziejski. Paweł A PA; Sassek. Maciej M; Sliwowska. Joanna H JH

Key Findings

  • Kisspeptin-10 is expressed in mouse 3T3‑L1 cells and rat adipocytes
  • It inhibits cell proliferation, viability and adipogenesis, lowering PPAR‑γ and C/EBP‑β expression
  • It enhances lipolysis by increasing perilipin and hormone‑sensitive lipase, modulates glucose uptake, raises leptin and lowers adiponectin

Practical Outcomes

  • The study suggests kisspeptin‑10 could be a molecular lever to reduce fat cell formation and boost fat breakdown, but there’s no human data or dosing guidance yet. For biohackers, it’s a hint that targeting the kisspeptin pathway might someday aid weight‑loss or metabolic health, but more research is needed before practical use.

Summary

Researchers found that kisspeptin-10, a small protein, is made by fat cells and can slow down their growth, push them to break down fat, and change how they handle sugar. In lab tests on mouse cells and rat fat tissue, it reduced the signals that make new fat cells, increased enzymes that burn fat, and altered hormone release, but these results are only in cells, not people.

Abstract

Kisspeptin, which is encoded by the KISS1 gene and acts via GPR54, plays a role in the regulation of reproductive functions. Expression of KISS1 and GRPR54 has been found in peripheral tissues, including adipose tissue, and was shown to be influenced by metabolic status. We hypothesized that kisspeptin could be involved in regulation of lipid metabolism in the mouse 3T3-L1 cell line and in isolated rat adipocytes. First, we characterized expression profiles of KISS1 and GPR54 mRNA and proteins in adipose cells isolated from male rats. Secondly, we studied the effects of kisspeptin-10 on cell proliferation and survival in 3T3-L1 cells. Thirdly, we assessed the rapid action of kisspeptin-10 on lipid metabolism and glucose uptake using 3T3-L1 cells and rat primary adipocytes. Finally, we examined the effects of kisspeptin-10 on the secretion of leptin and adiponectin in rat adipocytes. We have found that: (1) KISS1 and GPR54 were expressed in mouse 3T3-L1 cells and isolated rat adipocytes; (2) kisspeptin-10: (i) inhibited cell proliferation, viability and adipogenesis in 3T3-L1 and decreased expression of PPAR-γ and CEBPβ-genes, which are involved in the differentiation processes and adipogenesis; (ii) increased lipolysis in 3T3-L1 cells and rat adipocytes by enhancing expression of periliphin and hormone-sensitive lipase; (iii) modulated glucose uptake and lipogenesis; (iv) stimulated leptin and decreased adiponectin secretion from rat adipocytes. Kisspeptin-10 could play a role in the regulation of lipid metabolism in mouse 3T3-L1 cells and rat adipocytes.

Study Information

Provider

pubmed

Year

2017

Date

2017-02-13T00:00:00.000Z

DOI

10.1007/s12020-017-1248-y

Citations

40

References

46