» Articles » PMID: 5283931

Regulation of Formation and Proposed Structure of the Factor Inhibiting the Release of Melanocyte-stimulating Hormone

Overview
Specialty Science
Date 1971 Jul 1
PMID 5283931
Citations 23
Authors
Affiliations
Soon will be listed here.
Abstract

Microsomal preparations from the stalk median eminence of female rats are shown to contain an enzymic activity that is responsible for the formation of MSH-release-inhibiting factor (MSH-R-IF). The amount of this activity remains constant throughout the estrous cycle. The corresponding mitochondrial preparations from the stalk median eminence contain another enzymic principle, estrous cycle-dependent, which competes with the enzyme present in the microsomal preparation for the same "substrate", and can thereby prevent the formation of MSH-R-IF. Several neurohypophyseal hormones, analogs, and peptide intermediates have been tested for their intrinsic MSH-R-IF activity and for their ability to be transformed into MSH-R-IF by incubation with microsomal preparations of stalk median eminence from male rats; it is concluded that the enzyme responsible for the formation of MSH-R-IF is an exopeptidase and that the release-inhibiting factor itself is a tripeptide. Oxytocin is converted by the incubation to (L)-prolyl-(L)-leucylglycinamide; nanogram amounts of this tripeptide inhibit the release of MSH from the pituitary both in vivo and in vitro.

Citing Articles

Roots and early routes of neuroendocrinology.

Rodriguez E, Guerra M, Blazquez J Cell Tissue Res. 2025; .

PMID: 39883141 DOI: 10.1007/s00441-024-03928-0.


Stapling Amantadine to Melanostatin Neuropeptide: Discovery of Potent Positive Allosteric Modulators of the D Receptors.

Silva-Reis S, Correia X, Costa-Almeida H, Pires-Lima B, Maronde D, Costa V ACS Med Chem Lett. 2023; 14(12):1656-1663.

PMID: 38116429 PMC: 10726482. DOI: 10.1021/acsmedchemlett.3c00264.


In vitro permeation of micronized and nanonized alaptide from semisolid formulations.

Opatrilova R, Cernikova A, Coufalova L, Dohnal J, Jampilek J ScientificWorldJournal. 2014; 2013:787283.

PMID: 24453907 PMC: 3881672. DOI: 10.1155/2013/787283.


Mass spectrometric quantification of MIF-1 in mouse brain by multiple reaction monitoring.

Kheterpal I, Kastin A, Mollah S, Yu C, Hsuchou H, Pan W Peptides. 2009; 30(7):1276-81.

PMID: 19540426 PMC: 3521590. DOI: 10.1016/j.peptides.2009.04.004.


Plasma beta-lipotropin levels in Parkinson's disease.

Wiesen M, Yahr M, Krieger D J Neural Transm. 1982; 53(1):75-82.

PMID: 6278076 DOI: 10.1007/BF01243521.


References
1.
MERRIFIELD R . Automated synthesis of peptides. Science. 1965; 150(3693):178-85. DOI: 10.1126/science.150.3693.178. View

2.
Ferrier B, Jarvis D, DU VIGNEAUD V . Deamino-oxytocin. Its isolation by partition chromatography on Sephadex and crystallization from water, and its biological activities. J Biol Chem. 1965; 240(11):4264-6. View

3.
Brooks C, Ishikawa T, Koizumi K, Lu H . Activity of neurones in the paraventricular nucleus of the hypothalamus and its control. J Physiol. 1966; 182(1):217-31. PMC: 1357467. DOI: 10.1113/jphysiol.1966.sp007820. View

4.
DU VIGNEAUD V, FLOURET G, Walter R . Synthesis and some biological properties of 4-valine-oxytocin and 1-deamino-4-valine-oxytocin. J Biol Chem. 1966; 241(9):2093-6. View

5.
Taleisnik S, Tomatis M . Antagonistic effect on melanocyte-stimulating hormone release of two neural tissue extracts. Am J Physiol. 1967; 212(1):157-63. DOI: 10.1152/ajplegacy.1967.212.1.157. View