From the Departamento de Farmacología y Toxicología,
CINVESTAV-IPN, Tepepan, México City.
Correspondence to Alfredo Meneses, PhD, AP Postal 22026, México 14000 DF.
AbstractSpontaneously hypertensive
rats (SHR) of 3 to 12 months of age learned and retrieved less
information than normotensive Wistar-Kyoto rats (WKY), although no
difference was found with animals from 18 and 24 months of age. The
combined influence of hypertension and aging had an additive
detrimental effect on cognitive functions. Notwithstanding these
deficiencies in learning and memory, SHR have seldom been used as a
model in the screening of drugs with therapeutic potential for
treatment of disorders of cognitive processes. Moreover, the calcium
channel blocker nimodipine has beneficial effects on learning in both
aged and hypertensive animals and humans. However, no attempt has been
made to investigate whether nimodipine can reverse the additive
deleterious effects of aging and hypertension in the same subject. We
recently reported that deteriorated animals (middle-aged and/or
hypertensive) chronically treated with nimodipine (via osmotic
minipumps) exhibit higher learning scores. This information indicates
that nimodipine can reverse the impairing effects of either aging or
hypertension on learning; the presence of the two conditions, however,
produces a severe impairment that can be partially reversed by this
drug. Therefore, we propose that mature and middle-aged SHR
represent a model for the screening of potentially useful drugs
in the treatment of learning disorders, probably associated with
hypertension and/or aging. Nevertheless, it must be remembered that the
SHR is a genetic model and the appearance of neural
disturbances could be a parallel genetic phenomenon and not
necessarily or exclusively related to hypertension per se.
© 1998 American Heart Association, Inc.
Scientific Contributions
Spontaneously Hypertensive Rats
A Potential Model to Identify Drugs for Treatment of Learning Disorders
Key Words: : rats, inbred SHR learning memory aging pharmacology models
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