F. Eng et al., LONG-TERM ALTERATIONS IN THE PERMEABILITY OF THE BLOOD-TESTIS BARRIERFOLLOWING A SINGLE INTRATESTICULAR INJECTION OF DILUTE AQUEOUS GLYCEROL, Journal of andrology, 15(4), 1994, pp. 311-317
The mechanism whereby glycerol exerts its antispermatogenic action is
not known. The objective of this study was to determine, with the use
of [H-3]inulin and [I-125]albumin by in vivo and in vitro methods, whe
ther glycerol exerts its effect by altering the permeability of the bl
ood-testis barrier (BTB). Adult male rats received a single intratesti
cular injection of either glycerol (10% or 20%; treated) or saline (co
ntrol), and 2, 4, 8, 26, and 56 weeks after treatment, either [H-3]inu
lin or [I-125]albumin was administered either by infusion or directly
to the testicular tissues. Radioactivity was measured in testicular ti
ssue, rete testis fluid, and seminiferous tubular fluid. Following in
vivo administration, the uptake of [H-3]inulin by seminiferous tubules
, rete testis fluid, and seminiferous tubule fluid was significantly g
reater in the treated than in the control testes at all times after tr
eatment. Radiolabeled inulin, injected into isolated testes or added t
o medium in which isolated tubules were incubated, accumulated at sign
ificantly higher levels in the seminiferous tubule compartment of trea
ted than control tissues. Rete testis fluid from treated testes, colle
cted by micropuncture following efferent duct ligation, contained abou
t 5- to 13-fold more radioactivity than fluid from controls. Following
infusion of 50 mu Ci of [I-125]albumin into the jugular vein, the acc
umulated radioactivity was significantly greater in testicular and epi
didymal tissues and in the seminiferous tubule fluid from treated than
from control animals. In all experiments, the significant differences
between treated and control were maintained during the period of 2-56
weeks following glycerol treatment. The results suggest that a single
intratesticular injection of dilute glycerol solution alters the perm
eability of the BTB to macromolecules such as inulin and albumin, and
the effect appears to be permanent.