2012
Boar sperm head membrane damage during cryopreservation evaluated by electron microscopy
SEDLÁČKOVÁ, Miroslava; P. PŘINOSILOVÁ; V. KOPECKÁ a J. HLAVICOVÁZákladní údaje
Originální název
Boar sperm head membrane damage during cryopreservation evaluated by electron microscopy
Autoři
SEDLÁČKOVÁ, Miroslava; P. PŘINOSILOVÁ; V. KOPECKÁ a J. HLAVICOVÁ
Vydání
Research in pig breeding, Kostelec nad Orlicí, Výzkumný ústav živočišné výroby, 2012, 1802-7547
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
30000 3. Medical and Health Sciences
Stát vydavatele
Česká republika
Utajení
není předmětem státního či obchodního tajemství
Označené pro přenos do RIV
Ano
Kód RIV
RIV/00216224:14110/12:00068283
Organizační jednotka
Lékařská fakulta
Klíčová slova anglicky
Boar; sperm; membrane; TEM; ultrastructure
Změněno: 15. 5. 2013 15:59, Soňa Böhmová
Anotace
V originále
As electron microscopy can reveal much smaller changes in plasma membrane integrity than optical methods, it appears to be a useful tool for evaluating semen quality or the damage inflicted on spermatozoa during preservation. By evaluating membrane integrity of the sperm head in 16 boars by transmission electron microscopy (TEM), it was found that the plasma membrane is very sensitive and tends to break in the acrosomal area but not in the rest of the sperm head. The earliest signs of injury to spermatozoa in the acrosomal part of the sperm head were observed in the plasma membrane that became swollen, broken or lost. The next damaged part of spermatozoa which is less sensitive than the plasma membrane is the acrosome and its external membrane. The freezing process caused a substantial increase in the degree of cell damage manifested as disturbed or missing plasma membrane, acrosomal reaction-like changes and unevenly distributed or lost acrosomal contents. The latter was not found in fresh semen. Using an appropriate buffer concentration for the fixatives applied during preparation of semen samples for TEM appeared as a very important factor due to the impact of their osmolality on plasma membrane integrity of sperm cells.