Effects of melanocortin-4 receptor agonists and antagonists on expression of genes related to reproduction in spotted scat, Scatophagus argus.
Jiang. Dong-Neng DN; Li. Jian-Tao JT; Tao. Ya-Xiong YX; Chen. Hua-Pu HP; Deng. Si-Ping SP; Zhu. Chun-Hua CH; Li. Guang-Li GL
Key Findings
- MC4R agonists (NDP‑MSH, THIQ) raise gnrh, fshb, and lhb gene expression in fish hypothalamus and pituitary
- MC4R antagonists (SHU9119, Ipsen 5i) suppress those same reproductive hormone genes
- Both effects were seen in cultured tissue and after injecting the compounds into live fish
Practical Outcomes
- The findings show MC4R can control reproductive hormone production in fish, but they don’t translate into actionable protocols for human longevity, metabolism, or performance. No dosage or safety guidance for people is provided, so the study isn’t directly useful for the biohacker community.
Summary
The study looked at how drugs that turn on or off a brain receptor called MC4R affect hormone genes linked to reproduction in a fish species. Turning the receptor on boosted hormone gene activity, while blocking it lowered the activity, both in lab tissue and live fish. This research is about fish biology and doesn’t give usable advice for human health or performance.
Abstract
Melanocortin-4 receptor (Mc4r) function related to reproduction in fish has not been extensively investigated. Here, we report on gene expression changes by real-time PCR following treatment with Mc4r agonists and antagonists in the spotted scat (Scatophagus argus). Using in vitro incubated hypothalamus, the Mc4r nonselective agonist NDP-MSH ([Nle<sup>4</sup>, D-Phe<sup>7</sup>]-α-melanocyte stimulating hormone; 10<sup>-6</sup> M) and selective agonist THIQ (N-[(3R)-1, 2, 3, 4-Tetrahydroisoquinolinium-3-ylcarbonyl]- (1R)-1-(4-chlorobenzyl)-2-[4-cyclohexyl-4-(1H-1,2,4-triazol-1-ylmethyl) piperidin-1-yl]-2-oxoethylamine; 10<sup>-7</sup> M) significantly increased the expression of gnrh (Gonadotropin releasing hormone), while the Mc4r nonselective antagonist SHU9119 (Ac-Nle-[Asp-His-DPhe/DNal(2')-Arg-Trp-Lys]-NH2; 10<sup>-6</sup> M) and selective antagonist Ipsen 5i (compound 5i synthesized in Ipsen Research Laboratories; 10<sup>-6</sup> M) significantly inhibited gnrh expression after 3 h of incubation. In incubated pituitary tissue, NDP-MSH and THIQ significantly increased the expression of fshb (Follicle-stimulating hormone beta subunit) and lhb (Luteinizing hormone beta subunit), while SHU9119 and Ipsen 5i significantly decreased fshb and lhb expression after 3 h of incubation. During the in vivo experiment, THIQ (1 mg/kg bw) significantly increased gnrh expression in hypothalamic tissue, as well as the fshb and lhb expression in pituitary tissue 12 h after abdominal injection. Furthermore, Ipsen 5i (1 mg/kg bw) significantly inhibited gnrh expression in hypothalamic tissue, as well as fshb and lhb gene expression in pituitary tissue 12 h after abdominal injection. In summary, Mc4r singling appears to stimulate gnrh expression in the hypothalamus, thereby modulating the synthesis of Fsh and Lh in the pituitary. In addition, Mc4r also appears to directly regulate fshb and lhb levels in the pituitary in spotted scat. Our study suggests that Mc4r, through the hypothalamus and pituitary, participates in reproductive regulation in fish.
Study Information
pubmed
2017
2017-02-14T00:00:00.000Z
10.1007/s00360-017-1062-0
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