TY - JOUR
T1 - Heat produces uteroplacental circulatory disturbance in pregnant rats through action of corticotropin releasing hormone (CRH)
AU - Nakamura, H.
AU - Nagase, H.
AU - Ogino, K.
AU - Hatta, K.
AU - Matsuzaki, I.
N1 - Funding Information:
This work was supported in part by a Grant-in Aid for Scientific Research (C; No. 09670382, B; No. 11470094) from the Ministry of Education, Sports, Science and Culture of Japan for 1997-2000. We are indebted to the president of Kanazawa University, Dr Akira Okada, for his kind support and interest regarding this work.
PY - 2000
Y1 - 2000
N2 - There is some evidence showing an existence of corticotropin releasing hormone (CRH) and opioid peptides, including β-endorphin (βEP), in human placenta, whereas physiological roles of the placental peptides in response to stress remain to be elucidated. To clarify the involvement of CRH and opioid system in the uteroplacental circulation in the pregnant rats exposed to heat, we examined the effects of heat and intravenous administration of CRH receptor antagonist α-helical CRH (9-41) on the uteroplacental blood flow, as well as blood CRH, and blood and placental βEP in pregnant rats. Heat did not change uterine blood flow in virgin rats, but reduced uteroplacental blood flow in pregnant rats. The reduced uteroplacental blood flow induced by heat in pregnant rats was reversed by the administration of α-helical CRH. Independent of the status of pregnancy, heat increased blood CRH, which was not reversed by α-helical CRH. Although heat did not change placental βEP, α-helical CRH reduced blood and placenta βEP in pregnant rats. These results suggest that the uteroplacental circulatory disturbance caused by heat is mediated by CRH, possibly through the involvement of CRH receptor in rat placenta. The placental opioid system seems unlikely to be involved in the mediation of uteroplacental circulation. (C) 2000 Harcourt Publisher Ltd.
AB - There is some evidence showing an existence of corticotropin releasing hormone (CRH) and opioid peptides, including β-endorphin (βEP), in human placenta, whereas physiological roles of the placental peptides in response to stress remain to be elucidated. To clarify the involvement of CRH and opioid system in the uteroplacental circulation in the pregnant rats exposed to heat, we examined the effects of heat and intravenous administration of CRH receptor antagonist α-helical CRH (9-41) on the uteroplacental blood flow, as well as blood CRH, and blood and placental βEP in pregnant rats. Heat did not change uterine blood flow in virgin rats, but reduced uteroplacental blood flow in pregnant rats. The reduced uteroplacental blood flow induced by heat in pregnant rats was reversed by the administration of α-helical CRH. Independent of the status of pregnancy, heat increased blood CRH, which was not reversed by α-helical CRH. Although heat did not change placental βEP, α-helical CRH reduced blood and placenta βEP in pregnant rats. These results suggest that the uteroplacental circulatory disturbance caused by heat is mediated by CRH, possibly through the involvement of CRH receptor in rat placenta. The placental opioid system seems unlikely to be involved in the mediation of uteroplacental circulation. (C) 2000 Harcourt Publisher Ltd.
UR - http://www.scopus.com/inward/record.url?scp=0033865598&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0033865598&partnerID=8YFLogxK
U2 - 10.1053/plac.2000.0536
DO - 10.1053/plac.2000.0536
M3 - Article
C2 - 10940201
AN - SCOPUS:0033865598
SN - 0143-4004
VL - 21
SP - 510
EP - 515
JO - Placenta
JF - Placenta
IS - 5-6
ER -