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1 Department of Biology, Asbury College, Wilmore 40390-1198; 2 Department of Physiology, College of Medicine, University of Kentucky, Lexington 40536-0298; and 3 Center for Biomedical Engineering, University of Kentucky, Lexington, Kentucky 40536-0298
We examined the effects of chronic
nicotine exposure and dietary salt on the arterial blood pressure (BP)
changes learned in response to an acute behavioral stress in the Dahl
salt-sensitive rat. Four groups were tested: low salt + vehicle;
low salt + nicotine; high salt + vehicle; and high salt + nicotine. Rats were fed a low-salt (0.08% NaCl) or a high-salt (8%
NaCl) diet for 4 wk; 2.4 mg · kg
1 · day
1
nicotine or vehicle was given via an implanted osmotic minipump for the
last 2 wk. All rats were conditioned by following one tone (CS+) with a
0.5-s tail shock; another tone (CS
) was never followed by shock. CS+
in low salt + vehicle and high salt + vehicle-treated rats
evoked an initial arterial BP increase (C1), a component of
the startle response, and an ensuing, smaller, but more sustained, pressor response (C2), which is acquired with training. In
these rats, both C1 and C2 evoked by CS
were
significantly smaller than those to CS+, demonstrating that these
groups discriminated between the two tests. Conversely, although the
low salt + nicotine-treated rats had both the C1 and
C2 components of the conditional arterial pressure
response, they did not discriminate between CS+ and CS
. Finally, the
high salt + nicotine group failed to both discriminate between
tones and acquire (i.e., learn) the C2 response. The
unconditional response to shock did not differ between groups. We
conclude that combined exposure to high salt and to nicotine inhibits
the salt-sensitive animal's acquisition of a learned conditional BP
response, perhaps because nicotine acts preferentially on those central
processes required for associative learning versus those involved in
orientating to external stimuli.
Pavlovian conditioning; learning; stress; tobacco smoking; hypertension; autonomic nervous system
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