Several technical procedures mere described for estimation of epididymal sp
erm concentration until today. In all of the described techniques, epididym
al material was drawn into a micro-pipette before counting procedure. We ai
med to proceed this stage without using any pipette because of the difficul
ty in aspirating very viscous epididymal material into a micro-pipette. For
measuring epididymal material we used a 2 mu l reservoir which me named as
a micro-spoon. It was filled with the epididymal material and layered in a
tube with Ringer's solution of 2 mi containing sodium hyaluronate. Then, i
t was mixed in order to obtain 1/1000 diluted suspension. Sperm cells in th
is suspension were counted on a Makler chamber under a light microscope. Th
e procedure was easy and time saving, compared to the other techniques. (C)
2000 Tohoku University Medical Press.