From the Department of Physiology, University of Melbourne, Parkville
(F.J.C., S.B.H.), and the Bone Marrow Transplant Unit, Alfred Hospital,
Prahran (M.K.), Victoria, Australia.
Correspondence to Stephen B. Harrap, Department of Physiology, University of Melbourne, Parkville, Victoria 3052, Australia. E-mail s.harrap{at}physiology.unimelb.edu.au
AbstractNerve growth factor (NGF)
determines sympathetic innervation of target tissues, and NGF levels
are increased in young spontaneously hypertensive rats (SHR).
Angiotensin can affect NGF levels, and the persistent
reduction in blood pressure after brief
angiotensin-converting enzyme inhibition in young SHR may
involve long-term changes in NGF and sympathetic innervation. We
measured the relative abundance of renal NGF mRNA by reverse
transcriptionpolymerase chain reaction in SHR during and after
treatment from 6 to 10 weeks of age with vehicle, perindopril (3 mg/kg
per day), the bradykinin B2 antagonist Hoe 140
(0.5 mg/kg per day), both perindopril and Hoe 140, or
angiotensin II (Ang II; 200 ng/kg per minute).
Glomerular filtration rates were estimated at 10 and 20
weeks of age. At 10 weeks of age, Ang II caused a significant
(P<.01) increase and perindopril caused a significant
(P<.01) decrease in renal NGF mRNA levels. Blockade of
the bradykinin B2 receptor during perindopril treatment
attenuated (P<.05) the reduction in NGF mRNA levels.
Renal NGF mRNA (P=.005) and blood pressure
(P<.001) remained significantly lower than control 10
weeks after perindopril treatment was stopped. The partial reduction in
blood pressure at 20 weeks of age in rats that had received perindopril
and Hoe 140 was not associated with any difference in renal NGF mRNA.
Perindopril-induced long-term reduction in renal NGF mRNA levels may
decrease sympathetic innervation and thereby contribute to the
long-term posttreatment blood pressure reduction.
© 1998 American Heart Association, Inc.
Scientific Contributions
Persistent Reduction in Renal Nerve Growth Factor mRNA After Perindopril Treatment of Young Spontaneously Hypertensive Rats
Key Words: nerve growth factor angiotensin-converting enzyme sympathetic nervous system bradykinin genetics
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