Testicular angiotensin converting enzyme (ACE) isozyme is likely to play im
portant functional roles in male reproduction. Several studies have shown t
hat ACE is released from human spermatozoa during capacitation and that ACE
is associated with reduced sperm motility. Recently, we established an ass
ay to detect testicular ACE activity in human spermatozoa. The purpose of t
his study was to determine if testicular ACE activity is related to sperm m
otility in human ejaculates. Semen samples were collected from 80 infertile
patients. According to the semen characteristics, they were divided into f
our (WHO) categories. Enzyme activities of ACE in spermatozoa (testicular A
CE) and seminal plasma (somatic ACE) were spectrophotometrically determined
. Total testicular ACE activity in spermatozoa was measured by solubilizati
on of spermatozoa with Triton X-100. Membrane testicular ACE activity was m
easured in a sperm : PBS suspension. Sperm concentration and sperm motility
were 136.6 +/- 154.1 x 10(6)/mL and 58.6 +/- 23.4%, respectively (mean SID
). Enzyme activities of membrane testicular ACE, total testicular ACE and s
omatic ACE were 0.273 +/- 1.219 muU/10(6) spermatozoa, 0.35 +/- 1.34 muU/10
(6) spermatozoa and 684.7 +/- 226.6 mU/mL, respectively. A negative correla
tion was observed between sperm motility and membrane testicular ACE activi
ty (p < 0.05). Membrane testicular ACE activity in 44 normal semen samples
was 0.04 <plus/minus>0.02 muU/10(6) spermatozoa, whilst that in 36 abnormal
semen samples was 0.24 +/- 0.42 muU/10(6) spermatozoa. There was a signifi
cant difference between these two groups (p < 0.01). Membrane testicular AC
E in sperm samples from normozoospermic men was significantly lower than th
at from oligoasthenozoospermic men (P < 0.05). These findings suggest that
testicular ACE is released from normal functional spermatozoa for them to h
ave fertilizing ability.