|
|
||||||||
Biology of Reproduction, Vol 26, 385-390, Copyright © 1982 by Society for the Study of Reproduction
ARTICLES |
JK Lu and HL Judd
Previous studies indicated that circulating 20 alpha- hydroxyprogesterone (20 alpha-OH-P) in cyclic female rats derived from enzymatic conversion of progesterone in corpus luteum tissue (Hashimoto and Wiest, 1969). A possibility of extraovarian conversion of progesterone to 20 alpha-OH-P also was revealed by our recent finding that placement of Silastic implants of progesterone produced not only high plasma progesterone but also 20 alpha-OH-P in ovariectomized (OVX), previously pseudo-pregnant, rats (Gilman et al., 1981). This study was performed to measure the amounts of serum 20 alpha-OH-P and progesterone in intact or adrenalectomized (ADX), cyclic female rats and in OVX, ADX or OVX-ADX animals with or without progesterone implants. Twenty-four-hour patterns of serum progestins revealed that OVX rats exhibited low progesterone secretion (3-6 ng/ml) and undetectable levels of 20 alpha-OH-P in the absence of ovaries. In intact, cyclic females, circulating concentrations of 20 alpha-OH-P were 4- to 6-fold greater than those or progesterone. ADX resulted in a partial reduction of progesterone but not 20 alpha-OH-P in the circulation. Placement of 4 cm Silastic implants of progesterone produced high serum concentrations of both progesterone (29 +/- 4 ng/ml, mean +/- SEM) and 20 alpha-OH-P (27 +/- 1 ng/ml) in OVX and OVX- ADX rats. These findings demonstrate that placement of progesterone implants into female rats produces high circulating concentrations of both progesterone and 20 alpha-OH-P, and indicate that an extraovarian and extra-adrenal system(s) for progestin conversion is functioning under persistently high circulating progesterone conditions. By this system, large amounts of circulating progesterone are transformed into a less potent progestational compound, 20 alpha-OH-P.
This article has been cited by other articles:
![]() |
P. E. Micevych, V. Chaban, J. Ogi, P. Dewing, J. K. H. Lu, and K. Sinchak Estradiol Stimulates Progesterone Synthesis in Hypothalamic Astrocyte Cultures Endocrinology, February 1, 2007; 148(2): 782 - 789. [Abstract] [Full Text] [PDF] |
||||
![]() |
I. Sakata, T. Tanaka, M. Yamazaki, T. Tanizaki, Z. Zheng, and T. Sakai Gastric estrogen directly induces ghrelin expression and production in the rat stomach. J. Endocrinol., September 1, 2006; 190(3): 749 - 757. [Abstract] [Full Text] [PDF] |
||||
![]() |
F. Shi, M. Ozawa, H. Komura, P. Yang, A. L. Trewin, R. J. Hutz, G. Watanabe, and K. Taya Secretion of Ovarian Inhibin and Its Physiologic Roles in the Regulation of Follicle-Stimulating Hormone Secretion during the Estrous Cycle of the Female Guinea Pig Biol Reprod, January 1, 1999; 60(1): 78 - 84. [Abstract] [Full Text] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |