An automated sperm morphometry analysis (ASMA) instrument was develope
d to obtain measurements of toxicant-induced changes in rat sperm head
morphometry. 1,3-dinitrobenzene (1,3-DNB), a testicular toxicant know
n to affect sperm parameters, was used. Twelve-week-old Sprague-Dawley
rats were allocated to a control (C) and to two 1,3-DNB treatment gro
ups (T1 = 15 mg/kg; T2 = 25 mg/kg). 1,3-DNB was administered as a sing
le dose by gavage, and animals were sacrificed 22 days after exposure.
Sperm were collected, and morphology smears were made by a standard m
ethod. One hundred sperm heads were digitized on each slide, and 8 met
ric measurements were automatically reported. All measurements tended
to decrease in a dose-dependent manner with increasing doses of 1,3-DN
B. All values for total width (W-a) and interior width (W-e) were sign
ificantly different from one another. Wa/L was significantly larger in
the control than in T1 or T2, and symmetry (S = W-b/W-a) was signific
antly smaller in the control than in T1 or T2. Multivariate cluster an
alysis revealed three subpopulations that were also visually distinct.
Subpopulation no. 1 was normal, based on published descriptions of no
rmal rat sperm; subpopulation no. 2 was abnormal with a flattened curv
ature and a normal length; subpopulation no. 3 was abnormal with a for
eshortened length and a flattened curvature. T1 and T2 contained signi
ficantly more sperm from subpopulation no. 2 and no. 3 than C (T1 = 22
% and T2 = 34% vs. C = 8% by cluster analysis). C had 93% normal sperm
, while the treatments had 78% and 66%, respectively. Based on these f
indings, we conclude that ASMA is an efficient and accurate method of
sperm morphometry analysis that may improve our ability to detect sper
m biomarkers of reproductive health.