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Updated: Jun 23, 2026

Assessment of Sexual Behavior of Male Mice
Published on: March 5, 2020
Endomorphin-1, effects on male sexual behavior
Leticia Parra-Gámez1, A Alejandro García-Hidalgo, A Salazar-Juárez
1Facultad de Medicina, Universidad Nacional Autónoma de México, Ciudad Universitaria, CP 04510, México. gamezlp@gmail.com
Endomorphin-1 (EM-1), an opioid peptide, significantly alters male rat sexual behavior by increasing ejaculation latency and reducing ejaculations. These effects were blocked by naloxone, confirming the role of mu-opioid receptors.
Area of Science:
- Neuroscience
- Behavioral Endocrinology
- Pharmacology
Background:
- Endogenous opioid peptides modulate various physiological processes.
- Endomorphin-1 (EM-1) is a selective agonist for the mu-opioid receptor.
- Opioid involvement in sexual behavior is suggested but requires further elucidation.
Purpose of the Study:
- To investigate the effects of endomorphin-1 (EM-1) on male rat copulatory behavior.
- To determine the role of mu-opioid receptors in mediating these effects.
Main Methods:
- Intracerebroventricular injections of varying doses of EM-1 in Wistar rats.
- Measurement of sexual behavior parameters including ejaculation latency and interintromission interval.
- Assessment of EM-1 effects following pretreatment with the opioid antagonist naloxone.
Main Results:
- EM-1 administration dose-dependently increased ejaculation latency and interintromission interval.
- EM-1 reduced the number of ejaculations observed during the testing period.
- Naloxone pretreatment completely blocked the effects of EM-1 on sexual behavior.
Conclusions:
- Activation of mu-opioid receptors by EM-1 significantly modifies male sexual behavior parameters.
- These findings confirm the release and function of endogenous opioids during sexual activity.
- Opioid systems, particularly via mu-receptors, play a crucial role in regulating ejaculation.
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