Analyze Diet
Urology2003; 62(2); 357-361; doi: 10.1016/s0090-4295(03)00253-x

Muscarinic receptor subtypes mediate vasorelaxation in isolated horse deep dorsal penile vein.

Abstract: To investigate the effect of acetylcholine (ACh) on horse deep dorsal penile vein and to characterize the muscarinic receptor subtypes involved in this response. Methods: Vein rings were mounted in an organ bath chamber, and the isometric tension was recorded. Results: In phenylephrine-contracted veins, ACh (1 nM to 1 microM) induced endothelium-dependent relaxation. The muscarinic receptor antagonist, atropine, produced parallel rightward shifts of the ACh response curves (pA2 = 10.04; pK(B) = 9.98). Carbachol (10 nM to 100 microM) also evoked relaxation in the vein segments, but showed a lower potency and similar relaxation to that induced by ACh. Pirenzepine, the high, intermediate, and low-affinity antagonist for M1, M3, and M2 receptors, respectively, inhibited ACh and carbachol-induced relaxation, yielding pA2 values of 7.51 and 7.37, and pK(B) values of 7.38 and 7.28, respectively. Methoctramine, a high-affinity M2 antagonist, showed no significant effect on the response to ACh. However, a high-affinity M3 antagonist, pFHHSiD, potently blocked the relaxation induced by carbachol and ACh, yielding pA2 and pK(B) values of 7.72 and 7.70 for pFHHSiD against ACh, respectively, and of 7.77 and 7.65 against carbachol, respectively. Conclusions: These results indicate that ACh induces an endothelium-dependent relaxation in horse deep dorsal penile vein. The antagonist profile suggests that M3 muscarinic receptors mediate ACh-induced relaxation in this tissue.
Publication Date: 2003-08-02 PubMed ID: 12893364DOI: 10.1016/s0090-4295(03)00253-xGoogle Scholar: Lookup
The Equine Research Bank provides access to a large database of publicly available scientific literature. Inclusion in the Research Bank does not imply endorsement of study methods or findings by Mad Barn.
  • Journal Article

Summary

This research summary has been generated with artificial intelligence and may contain errors and omissions. Refer to the original study to confirm details provided. Submit correction.

The research examines the impact of acetylcholine (ACh) on horse deep dorsal penile vein and identifies the muscarinic receptor types that participate in this reaction. The study found that ACh triggers a relaxation response in the veined endothelium, orchestrated through M3 muscarinic receptors.

Research Methodology

  • The researchers utilized an organ bath chamber to study the vein rings in isolation and accurately record isometric tension. This procedure ensures a controlled environment where only the effect of acetylcholine can be observed without any external influences.
  • The vein rings were contracted using phenylephrine, and varying doses of ACh were introduced to induce endothelium-dependent relaxation.
  • The effects of ACh on the veins were studied in comparison to the effects of atropine, a muscarinic receptor antagonist.

Results and Interpretation

  • ACh was found to induce endothelium-dependent relaxation in the veins. Atropine, a muscarinic receptor antagonist, produced parallel rightward shifts of the response curves, suggesting an antagonistic effect.
  • Similar tests were conducted with Carbachol, which also induced relaxation, but with less potency than ACh.
  • Pirenzepine, an antagonist for M1, M3, and M2 receptors, was found to inhibit ACh and carbachol-induced relaxation.
  • A high-affinity M3 antagonist, pFHHSiD, significantly blocked relaxation induced by both carbachol and ACh. In contrast, Methoctramine, a high-affinity M2 antagonist, showed no significant effect on the ACh response.

Conclusions

  • The research concludes that ACh triggers an endothelium-dependent relaxation response in the horse deep dorsal penile vein and that M3 muscarinic receptors are key mediators of this response.
  • The researchers deduced that ACh-induced relaxation is dependent on the activity of M3 muscarinic receptors based on the findings that pFHHSiD (a high-affinity M3 antagonist) blocks this relaxation significantly.
  • This study marks an important exploration into the role of muscarinic receptors, particularly M3 type, in vasorelaxation, and can serve as a reference for future studies on the topic.

Cite This Article

APA
Martínez AC, Hernández M, Rivera L, Recio P, García-Sacristán A, Benedito S. (2003). Muscarinic receptor subtypes mediate vasorelaxation in isolated horse deep dorsal penile vein. Urology, 62(2), 357-361. https://doi.org/10.1016/s0090-4295(03)00253-x

Publication

ISSN: 1527-9995
NlmUniqueID: 0366151
Country: United States
Language: English
Volume: 62
Issue: 2
Pages: 357-361

Researcher Affiliations

Martínez, Ana Cristina
  • Sección Departamental de Fisiología, Facultad de Farmacia, Universidad Complutense, Madrid, Spain.
Hernández, Medardo
    Rivera, Luis
      Recio, Paz
        García-Sacristán, Albino
          Benedito, Sara

            MeSH Terms

            • Acetylcholine / pharmacology
            • Animals
            • Endothelium, Vascular / physiology
            • Horses
            • In Vitro Techniques
            • Male
            • Muscarinic Antagonists / pharmacology
            • Muscle Relaxation / drug effects
            • Muscle Relaxation / physiology
            • Muscle, Smooth, Vascular / drug effects
            • Muscle, Smooth, Vascular / physiology
            • Penis / blood supply
            • Receptors, Muscarinic / metabolism
            • Receptors, Muscarinic / physiology
            • Vasodilation / drug effects
            • Vasodilation / physiology
            • Vasodilator Agents / pharmacology
            • Veins

            Citations

            This article has been cited 1 times.
            1. Cripps SM, Marshall SA, Mattiske DM, Ingham RY, Pask AJ. Estrogenic endocrine disruptor exposure directly impacts erectile function. Commun Biol 2024 Apr 2;7(1):403.
              doi: 10.1038/s42003-024-06048-1pubmed: 38565966google scholar: lookup