Dh. Wiley et al., Neonatal sympathectomy reduces adult blood pressure and cardiovascular pathology in Y chromosome consomic rats, BLOOD PRESS, 8(5-6), 1999, pp. 300-307
The hypothesis was tested that the sympathetic nervous system (SNS) develop
mentally influences circulating testosterone (T), systolic blood pressure (
SBP) and cardio-renal pathology in SHR/y animals. A sympathoplegic drug, gu
anethidine, and an antibody to nerve growth factor were administered to WKY
and borderline hypertensive SHR/y male rats (n = 20/group) for the first 3
weeks of lift; control groups (n = 20/group) received saline. SBP, serum T
and luteinizing hormone (LH) were measured. SBP in the WKY and SHR/y sympa
thectomy (sympx) groups decreased 10 mmHg (p < 0.001) and 50 mmHg (p < 0.00
1), respectively, when compared to their control groups. Serum T levels in
the sympx WKY group were lower (p < 0.01) than those in controls, and the r
ise of T typically observed in SWR/y from weeks 6-8 was delayed in the symp
x SHR/y group, similar to the pattern in WKY. Serum LH levels were increase
d in the sympx WKY group, but not in the SHR/y group. Sympx caused a greate
r reduction in renal glomerular changes (p < 0.01), coronary artery collage
n deposition (p < 0.01) and myocardial fibrosis (p < 0.01) in SHR/y than WK
Y mts. In conclusion the SHR Y chromosome has a locus that enhances SNS act
ivity, which can raise SBP and result in renal and cardiovascular tissue da
mage.