At first, we investigated whether both
beta-endorphin release level in the hypothalamus and body temperature can be altered after intracerebroventricular (i.c.v.) injection of either
lipopolysaccharide (LPS),
interleukin-1beta (IL-1beta), or
prostaglandin E(2) (
PGE(2)) in rats. It was found that in the rat, i.c.v. administration of either LPS (0.5 microg in 10 microl), IL-1beta (10 ng in 10 microl), or
PGE(2) (200 ng in 10 microl), in addition to producing
fever, upregulated the immunoreactivity of
beta-endorphin in the preoptic anterior hypothalamus of rat brain. Secondarily, we assessed whether the
fever induced by either LPS, IL-1beta, or
PGE(2) can be altered by pretreatment with
buprenorphine (an
opioid receptor antagonist). The results revealed that i.c.v. administration of
buprenorphine (1 - 10 microg in 10 microl) alone had an insignificant effect on the body temperature. However, the
fever induced by i.c.v. injection of either LPS, IL-1beta, or
PGE(2) was significantly attenuated by pretreatment with i.c.v. injection of
buprenorphine 1 h before the
pyrogen injection in rats. The results suggest that
pyrogens enhance
beta-endorphin release in the hypothalamus and trigger
fever which can be attenuated by
buprenorphine, an
opioid receptor antagonist.