z-logo
open-access-imgOpen Access
Decreased sperm function of patients with myotonic muscular dystrophy
Author(s) -
María Luisa Hortas,
José Antonio Castilla,
Moran Gil,
Juan Antonio Maldonado Molina,
Manuela Garrido,
M Morell,
Maximino Redondo
Publication year - 2000
Publication title -
human reproduction
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.446
H-Index - 226
eISSN - 1460-2350
pISSN - 0268-1161
DOI - 10.1093/humrep/15.2.445
Subject(s) - capacitation , sperm , acrosome , acrosome reaction , andrology , myotonic dystrophy , biology , muscular dystrophy , medicine , endocrinology , genetics
Myotonic muscular dystrophy (MMD) is a genetic disease caused by a defective enzyme, myotoninkinase. Male patients with MMD are reported to have reduced fertility. The purpose of this work was to study sperm capacitation and acrosome reaction in the ejaculates of sterile males with MMD and of healthy 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 content and outer acrosomal membrane in the spermatozoa of each group were analysed. Both the capacitation and the acrosome reaction in the spermatozoa of the MMD group were deficient and these findings strongly suggest that these anomalies may account for the sterility of these patients.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom