Patients suffering from diabetes mellitus often develop reproductive d
ysfunction including anovulation, infertility and disrupted pregnancy.
The biochemical basis of these phenomena is yet to be provided. The c
urrent study utilizes a neuroendocrine paradigm involving an in vitro
microdissection technique in conjunction with jugular catheterization
to examined the proestrus dynamics of norepinephrine (NE) and the preo
vulatory luteinizing hormone (LH) surge in streptozotocin (STZ) treate
d female rats, an animal model for insulin dependent diabetes mellitus
. Radioimmunoassays revealed that in control subjects LH was at basal
level during the morning of proestrus (900-1200 h); the first signific
ant increase in the level of this pituitary hormone occurred at 1400-1
500 h. A maximum peak concentration of LH was attained at 1700 h. In c
ontrast, plasma levels of LH in diabetic subjects showed the first sig
nificant increase at 1500 h and peaked at 2000 h. The peak of the LH c
urve in diabetic rats was reduced by about 65% with a 3 h shift to the
right. Alpha-methyl-p-tyrosine-induced blockade of newly synthesized
NE-based assay showed that NE turnover rates in several hypothalamic n
uclei (e.g. medial preoptic nucleus, MPN; median eminence, ME; suprach
iasmatic nucleus, SCN; arcuate nucleus, AN) of control subjects were a
t basal level during the morning of proestrus (0900-1100 h). However,
they increased by the 1200-1400 h interval and remained elevated durin
g the 1500-1700 h. This time dependent increase in hypothalamic NE tur
nover rates during proestrus was not observed in the STZ diabetic rats
. Most of the above metabolic derangements were partially reversed fol
lowing th institution of insulin replacement therapy. Overall, our dat
a support the concept that the endocrine abnormalities (e.g. infertili
ty, delayed preovulatory LH surge) in diabetes are due, at least in pa
rt, to a functional deficit in noradrenergic neurons within the hypoth
alamus.