H. Nakamura et al., OPIOID-PEPTIDES MEDIATE HEAT STRESS-INDUCED IMMUNOSUPPRESSION DURING PREGNANCY, American journal of physiology. Regulatory, integrative and comparative physiology, 43(3), 1998, pp. 672-676
To clarify the involvement of the opioid system in enhanced immunosupp
ression induced by heat stress during pregnancy, we examined the effec
ts of heat exposure and intraperitoneal administration of opioid recep
tor antagonist naloxone on beta-endorphin (beta-EP) in blood, pituitar
y lobes, and placenta as well as splenic natural killer cell activity
(NKCA) and placental steroids in pregnant rats at 15-16 days gestation
. Two-way analysis of variance revealed significant increases in blood
beta-EP induced by heat and naloxone and a significant interaction be
tween heat and naloxone on blood beta-EP and progesterone (P). Whereas
heat reduced NKCA, intraperitoneal administration of naloxone reverse
d it. Significant increases in blood and placental beta-EP induced by
both heat and naloxone administration and a significant interaction on
blood and placental beta-EP was observed. These results suggest that
immunosuppression produced by heat stress during pregnancy is mediated
by the opioid system. A positive correlation between beta-EP in blood
and placenta during heat and naloxone administration suggests that in
creased placental beta-EP during heat results in hypersecretion of bet
a-EP into blood. P increased by heat during pregnancy may be involved
in the immunosuppression.