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Molecular reproduction and development2005; 73(1); 1-8; doi: 10.1002/mrd.20341

Proopiomelanocortin gene expression and beta-endorphin localization in the pituitary, testis, and epididymis of stallion.

Abstract: Proopiomelanocortin (POMC) is a precursor protein that contains the sequences of several bioactive peptides including adrenocorticotropin (ACTH), beta-endorphin (beta-EP), and melanocyte-stimulating-hormone (MSH). POMC is synthesized in the pituitary gland, brain, and many peripheral tissues. Immunoreactive POMC-derived peptides as well as POMC-like mRNA have been evidenced in several nonpituitary tissues, thus suggesting that POMC is actively synthesized by these tissues. The present study was aimed at evaluating if also in the case of stallion POMC-derived peptide, beta-EP, is produced locally in the testis, thus playing effects in a paracrine/autocrine fashion. To investigate this hypothesis the POMC gene expression was analyzed using 3' RACE-PCR and Northern Blot approaches in the testis and epididimys of stallion; moreover, immunocytochemical localization for beta-EP was also performed through confocal laser microscopy. The immunofluorescence results showed a positive beta-EP reaction not only in cellular nest of pituitary but also in the testis and genital tract of stallion, which function could be related with sperm mobility. Such role seem not to be no dependent on the peptide synthesized locally, because the molecular biology approach demonstrated the presence of POMC transcript in the pituitary only. In fact the Northern Blot analysis showed the presence of a single POMC transcript in the pituitary while no signal was detected in the testis and epididimys. The same results were obtained by applied 3' RACE-PCR analysis. In conclusion, opioid-derived peptide beta-EP is present in the genital tract of stallion, but is not locally produced as in other mammalian, and nonmammalian models; its possible biological function at testicular level could be linked to a long-loop feed-back mechanisms.
Publication Date: 2005-09-24 PubMed ID: 16177984DOI: 10.1002/mrd.20341Google Scholar: Lookup
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  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

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This study examines whether the peptide beta-endorphin, derived from the Proopiomelanocortin (POMC) protein, is locally produced in the testes of stallions. The researchers found beta-endorphin present in the genital tract but discovered it wasn’t produced locally, suggesting a role in long-loop feedback mechanisms.

Understanding POMC and the Research Objective

  • Proopiomelanocortin (POMC) is a protein precursor for several biologically significant peptides, including adrenocorticotropin (ACTH), beta-endorphin (beta-EP), and melanocyte-stimulating-hormone (MSH).
  • This protein is synthesized in the pituitary gland, brain, and various peripheral tissues. Several non-pituitary tissues show evidence of immunoreactive POMC-derived peptides and POMC-like mRNA, indicating active POMC synthesis.
  • The study aimed to determine if the testes of stallions also locally produce the POMC-derived peptide, beta-EP, resulting in paracrine or autocrine effects. This hypothesis was investigated using the POMC gene expression.

Methodology of the Study

  • POMC gene expression within the testes and epididymis of the stallion was analyzed using 3′ RACE-PCR and Northern Blot techniques.
  • Beta-EP was further localized using immunocytochemical methods via confocal laser microscopy.

Research Findings

  • The immunofluorescence results indicated a positive beta-EP reaction not only in the cellular nest of the pituitary but also in the stallion’s testes and genital tract. This led the researchers to consider a potential function for beta-EP related to sperm mobility in stallions.
  • However, this function does not appear to rely on locally synthesized peptide, as established through molecular biology techniques detecting the presence of POMC transcripts only in the pituitary.
  • The Northern Blot analysis revealed a single POMC transcript in the pituitary, with no signal detected in the testes and epididymis- a finding also confirmed by the applied 3′ RACE-PCR analysis.

Conclusion of the Study

  • The study concluded that while the opioid-derived peptide beta-EP is present in the stallion’s genital tract, it isn’t produced locally as in other mammalian and nonmammalian models.
  • Its potential biological function at the testicular level could be connected to long-loop feedback mechanisms, where signals from end products of a process further influence the system from which they are produced.

Cite This Article

APA
Soverchia L, Mosconi G, Ruggeri B, Ballarini P, Catone G, Degl'Innocenti S, Nabissi M, Polzonetti-Magni AM. (2005). Proopiomelanocortin gene expression and beta-endorphin localization in the pituitary, testis, and epididymis of stallion. Mol Reprod Dev, 73(1), 1-8. https://doi.org/10.1002/mrd.20341

Publication

ISSN: 1040-452X
NlmUniqueID: 8903333
Country: United States
Language: English
Volume: 73
Issue: 1
Pages: 1-8

Researcher Affiliations

Soverchia, L
  • Dipartimento di Medicina Sperimentale e Sanità Pubblica, Università degli Studi di Camerino, via Scalzino 3, Camerino (MC), Italia.
Mosconi, G
    Ruggeri, B
      Ballarini, P
        Catone, G
          Degl'Innocenti, S
            Nabissi, M
              Polzonetti-Magni, A M

                MeSH Terms

                • Animals
                • Base Sequence
                • Blotting, Northern
                • Epididymis / metabolism
                • Horses / metabolism
                • Humans
                • Male
                • Microscopy, Confocal
                • Microscopy, Fluorescence
                • Molecular Sequence Data
                • Pituitary Gland / metabolism
                • Polymerase Chain Reaction
                • Pro-Opiomelanocortin / biosynthesis
                • Pro-Opiomelanocortin / genetics
                • Testis / metabolism
                • beta-Endorphin / metabolism

                Citations

                This article has been cited 4 times.
                1. Estomba H, Muñoa-Hoyos I, Gianzo M, Urizar-Arenaza I, Casis L, Irazusta J, Subirán N. Expression and Localization of Opioid Receptors in Male Germ Cells and the Implication for Mouse Spermatogenesis. PLoS One 2016;11(3):e0152162.
                  doi: 10.1371/journal.pone.0152162pubmed: 27031701google scholar: lookup
                2. Subirán N, Casis L, Irazusta J. Regulation of male fertility by the opioid system. Mol Med 2011;17(7-8):846-53.
                  doi: 10.2119/molmed.2010.00268pubmed: 21431247google scholar: lookup
                3. Bodnar RJ. Endogenous opiates and behavior: 2006. Peptides 2007 Dec;28(12):2435-513.
                4. Vassoler FM, Wimmer ME. Consequences of Parental Opioid Exposure on Neurophysiology, Behavior, and Health in the Next Generations. Cold Spring Harb Perspect Med 2021 Oct 1;11(10).
                  doi: 10.1101/cshperspect.a040436pubmed: 32601130google scholar: lookup