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Melanotan-I

Afamelanotide, MT-I, [Nle4-D-Phe7]-α-MSH, Scenesse, CUV-1647

Quick Stats
Studies 225
Trials 100
Score 1
2016 pubmed 36 citations

Molecular cloning, tissue distribution, and pharmacological characterization of melanocortin-4 receptor in spotted scat, Scatophagus argus.

Li. Jian-Tao JT; Yang. Zhao Z; Chen. Hua-Pu HP; Zhu. Chun-Hua CH; Deng. Si-Ping SP; Li. Guang-Li GL; Tao. Ya-Xiong YX

Key Findings

  • The fish MC4R gene (SAMC4R) was cloned and encodes a 327‑amino‑acid protein similar to other fish MC4Rs.
  • SAMC4R is expressed in brain, pituitary, gonads and many peripheral tissues, with sex‑dependent patterns.
  • SAMC4R binds α‑MSH, NDP‑MSH and ACTH with higher affinity than human MC4R, but the synthetic agonist THIQ does not bind it.

Practical Outcomes

  • This study doesn’t change how biohackers should use melanotan‑I. It confirms that MC4R is a target for α‑MSH‑type peptides, but offers no new dosing, safety, or performance guidance for humans.

Summary

Scientists cloned the MC4R gene from a fish and studied how it reacts to several melanocortin‑related peptides, including the tanning peptide α‑MSH. The fish receptor works similarly to human MC4R but shows some differences in how strongly it binds these compounds. The work is basic research and doesn’t give any direct tips for using melanotan‑I in people.

Abstract

Melanocortin-4 receptor (MC4R) plays an important role in the regulation of food intake and energy expenditure in mammals. The functions of the MC4R in fish have not been investigated extensively. We herein reported on the cloning, tissue distribution, and pharmacological characterization of spotted scat (Scatophagus argus) MC4R (SAMC4R). It consisted of a 984bp open reading frame predicted to encode a protein of 327 amino acids. Sequence analysis revealed that SAMC4R was highly homologous (>80%) at amino acid levels to several teleost MC4Rs. Phylogenetic analyses showed that SAMC4R was closely related to piscine MC4R. Using RT-PCR, we showed that in addition to brain, pituitary, and gonads, mc4r mRNA was also widely expressed in peripheral tissues of spotted scat in sexually divergent pattern. With human MC4R (hMC4R) as a control, several agonists including α-melanocyte stimulating hormone (α-MSH), [Nle(4), D-Phe(7)]-α-MSH (NDP-MSH), adrenocorticotropic hormone (ACTH) and THIQ (N-[(3R)-1,2,3,4-tetrahydroisoquinolinium3-ylcarbonyl]-(1R)-1-(4-chlorobenzyl)-2-[4-cyclohexyl-4-(1H-1,2,4-triazol-1-ylmethyl)piperidin-1-yl]-2-oxoethylamine), were used to investigate the binding and signaling properties of SAMC4R. The results showed that SAMC4R bound NDP-MSH with the highest affinity followed by ACTH (1-24) and α-MSH. Similar ranking was also found for hMC4R, although SAMC4R had two to five-fold higher affinities for these ligands. THIQ did not displace NDP-MSH from SAMC4R, different from hMC4R. α-MSH, NDP-MSH, and ACTH (1-24) were identified as potent agonists to stimulate cAMP generation followed by THIQ in SAMC4R. The availability of SAMC4R and its pharmacological characteristics will facilitate the investigation of its function in regulating diverse physiological processes in spotted scat.

Study Information

Provider

pubmed

Year

2016

Date

2016-04-11T00:00:00.000Z

DOI

10.1016/j.ygcen.2016.04.010

Citations

36

References

67