Mi. Colado et al., INVOLVEMENT OF CENTRAL SEROTONERGIC PATHWAYS IN ANALGESIA ELICITED BYSALMON-CALCITONIN IN THE MOUSE, European journal of pharmacology, 252(3), 1994, pp. 291-297
The contribution of central serotonergic pathways to the analgesic act
ivity induced by salmon calcitonin in the writhing test was investigat
ed. Salmon calcitonin was administered to mice after lesioning of the
ascending and descending serotonergic pathways by means of i.p. admini
stration of p-chloroamphetamine (40 mg/kg, for 2 days) or p-chlorophen
ylalanine (300 mg/kg, for 3 days). The analgesic effect induced by sal
mon calcitonin at the doses of 10 and 20 IU/kg was not evident in mice
previously treated with p-chloroamphetamine or p-chlorophenylalanine.
However, the analgesic effect of salmon calcitonin 40 IU/kg was not s
ignificantly modified by p-chloroamphetamine or p-chlorophenylalanine
pretreatment. Salmon calcitonin did not alter the depletion of 5-hydro
xytryptamine (5-HT) and 5-hydroxyindoleacetic acid after p-chloroamphe
tamine or p-chlorophenylalanine administration. Similarly, this hormon
e did not change the NSD 1015-induced accumulation of 5-hydroxytryptop
han or the tranylcypromine-induced accumulation of 5-HT. These results
indicate that although salmon calcitonin does not influence the synth
esis and metabolism of 5-HT, it does require the integrity of the sero
tonergic system in order to cause analgesia.