L. Uphouse et al., AGONIST ACTIVATION OF 5-HT1A RECEPTORS IN THE MEDIAN RAPHE NUCLEUS AND FEMALE RAT LORDOSIS BEHAVIOR, Brain research, 668(1-2), 1994, pp. 271-275
Proestrous rats were infused unilaterally into the median raphe nucleu
s with 200-2,000 ng of the 5-HT1A agonist, 8-hydroxy-2-(di-n-propylami
no)tetralin (8-OH-DPAT). Inhibition of the lordosis to mount ratio occ
urred within 15 and 10 min, respectively, following infusion with 1,00
0 or 2,000 ng of the drug. Infusion of 2,000 ng of the 5-HT2 agonist,
(+/-)-(2,5-dimethoxy-4-iodopbenyl)-2-aminopropane HCl (DOI), or 4,000
ng 5-HT (creatinine sulfate) failed to substantially reduce lordosis b
ehavior.