Decreased sperm function of patients with myotonic muscular dystrophy

Citation
Ml. Hortas et al., Decreased sperm function of patients with myotonic muscular dystrophy, HUM REPR, 15(2), 2000, pp. 445-448
Citations number
20
Categorie Soggetti
Reproductive Medicine","da verificare
Journal title
HUMAN REPRODUCTION
ISSN journal
02681161 → ACNP
Volume
15
Issue
2
Year of publication
2000
Pages
445 - 448
Database
ISI
SICI code
0268-1161(200002)15:2<445:DSFOPW>2.0.ZU;2-W
Abstract
Myotonic muscular dystrophy (MMD) is a genetic disease caused by a defectiv e enzyme, myotoninkinase. Male patients with MMD are reported to have reduc ed fertility. The purpose of this work was to study sperm capacitation and acrosome reaction in the ejaculates of sterile males with MMD and of health y males (control group). The expression of the specific D-mannose receptors was explored by microscopic examination and by flow cytometry analysis. In addition, the binding patterns of Pisum sativum (PSA) lectin to acrosome c ontent and outer acrosomal membrane in the spermatazoa of each group were a nalysed. Both the capacitation and the acrosome reaction in the spermatozoa of the MMD group were deficient and these findings strongly suggest that t hese anomalies may account for the sterility of these patients.