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- Title
Human sperm express cannabinoid receptor Cb1, the activation of which inhibits motility, acrosome reaction, and mitochondrial function.
- Authors
Rossato, M; Ion Popa, F; Ferigo, M; Clari, G; Foresta, C
- Abstract
Cannabinoids and endocannabinoids negatively influence sperm functions. These substances have been demonstrated in many mammalian tissues, including male and female reproductive tracts, and previous studies have shown the presence of functional receptors for cannabinoids in human sperm. The present study, by means of RT-PCR and Western blot techniques, demonstrates that human sperm express the CB(1), but not CB(2), cannabinoid receptor (CB-R) subtype located in the head and middle piece of the sperm. The activation of this receptor by anandamide reduces sperm motility and inhibits capacitation-induced acrosome reaction. Activation of the CB(1)-R did not induce any variation in sperm intracellular calcium concentrations, but produced a rapid plasma membrane hyperpolarization that was reduced by the K(+) channel blocker tetraethylammonium. The effects of anandamide on human sperm motility were dependent on the reduction of sperm mitochondrial activity as determined by rhodamine 123 fluorescence. The specificity of anandamide effects in human sperm were confirmed by the effects of the CB(1)-R antagonist SR141716. These findings provide additional evidence that human sperm express functional CB(1)-R, the activation of which negatively influences important sperm functions, and suggest a possible role for the cannabinoid system in the pathogenesis of some forms of male infertility.
- Subjects
MITOCHONDRIAL physiology; OVUM physiology; SPERMATOZOA physiology; AMIDES; ARACHIDONIC acid; CELL receptors; COMPARATIVE studies; CONCEPTION; DRUGS; HETEROCYCLIC compounds; RESEARCH methodology; MEDICAL cooperation; MITOCHONDRIA; NEUROTRANSMITTERS; OVUM; PIPERIDINE; RESEARCH; SPERMATOZOA; SPERM motility; UNSATURATED fatty acids; EVALUATION research; PHARMACODYNAMICS; CELL physiology
- Publication
Journal of Clinical Endocrinology & Metabolism, 2005, Vol 90, Issue 2, p984
- ISSN
0021-972X
- Publication type
journal article
- DOI
10.1210/jc.2004-1287