Hypertension, Vol 23, 765-773, Copyright © 1994 by American Heart Association
CF Deschepper, JS Li, EL Schiffrin and SA Welner
Hypothalami from fetal rats were grafted into the third ventricle of four
strains of adult rats. Grafts from spontaneously hypertensive rats (SHR),
in contrast to grafts from Wistar-Kyoto (WKY) rats, induced an elevation of
systolic blood pressure and a thickening of the media of resistance
arteries, along with corresponding alterations in the contractile
properties of these vessels. However, no cardiac hypertrophy was observed.
The resistance arteries of rats grafted with hypothalamic from SHR also
displayed functional alterations that were similar to what is typically
found in the resistance arteries of young prehypertensive SHR, ie, an
increase in the sensitivity to cocaine and an impairment in the ability to
relax in the presence of acetylcholine. This suggests that the brain may
play a causal role in these alterations. Histological examination of
sections of brains grafted with previously labeled tissue revealed that (1)
there was no brain area that was systematically infiltrated by grafts from
SHR and not by grafts from WKY rats; (2) the volume of the transplants
appeared larger 2 weeks after the graft than the volume of the tissue
originally implanted; and (3) grafts from SHR were slightly larger,
displayed more individual foci, and extended farther along the
anteroposterior axis than grafts from WKY rats. In addition, glial cultures
derived from the hypothalami of SHR had a higher in vitro growth rate than
equivalent cultures from WKY rats. It is therefore possible that the
ability of brain grafts from SHR to induce hypertension is related to a
higher proliferative and/or migratory potential of nonneuronal cells within
the hypothalamus.
ARTICLES
Hypertension induced by brain grafts from fetal spontaneously hypertensive rats
Laboratory of Neurobiology and Vasoactive Peptides, Clinical Research Institute of Montreal, Quebec, Canada.
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