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Vol. 281, Issue 2, 775-784, 1997
INSERM CJF 94-05, INRA, Université Bordeaux II, Bordeaux,
France (A.K., S.A., O.B., A.R., P.M., F.C.), and
Institute of Cytology
and Genetics, Russian Academy of Science, 630090 Novosibirsk 90, Russia
(A.K.)
The spontaneously hypertensive (SHR) and Lewis (LEW) strains differ in
numerous behavioral tests, including the elevated plus-maze. In keeping
with the crucial role of central serotonin (5-HT) in anxiety, we
checked for strain differences regarding several determinants of 5-HT
activity. In addition to confirming that LEW rats displayed anxious
behaviors in the plus-maze compared with SHR, we found that in
vitro, central tryptophan hydroxylase activity was higher in
LEW rats than in SHR. However, ex vivo studies in
midbrains and hippocampi revealed that neither 5-HT synthesis nor 5-HT
and 5-hydroxyindoleacetic acid levels differed between strains.
[3H]8-Hydroxy-2-(di-n-propylamino)tetralin binding at
midbrain 5-HT1A autoreceptors and hippocampal
5-HT1A postsynaptic receptors, [3H]ketanserin
binding at cortical and striatal 5-HT2A receptors and
[3H]citalopram binding at midbrain and hippocampal 5-HT
transporters did not vary between strains. The inhibition of 5-HT
synthesis by 5-HT1A autoreceptor stimulation was similar in
both strains. Forepaw treading and flat body posture after
5-HT1A postsynaptic receptor stimulation were higher and
lower, respectively, in SHR than in LEW rats. Last,
1-(4-iodo-2,5-dimethoxy-phenyl)-2-aminopropane- and quipazine-elicited
head shakes, a 5-HT2A receptor-mediated response, were
increased in the SHR strain compared with the LEW strain; on the other
hand, 1-(3-chlorophenyl)piperazine triggered similar
5-HT2B/2C receptor-mediated decreases in motor activity in
the two strains. This study shows that although the low-anxiety (SHR)
and high-anxiety (LEW) strains vary in some aspects of 5-HT function,
key components such as the 5-HT1A autoreceptors are not
different.