Immunoreactive inhibin in follicular fluid is related to meiotic stage of the oocyte during final maturation of the porcine follicle
K.F. Miller, Sancai Xie, W. F. Pope
Abstract
K.F. Miller, Sancai Xie, W. F. Pope
Abstract
The concentration and content of inhibin was determined in individual porcine follicles from gilts ovariectomized at various times after the onset of estrus. In one experiment, gilts (n = 5) were ovariectomized at 0, 10, or 20 hr after the onset of estrus and the follicular fluids from all large follicles individually aspirated. In a second experiment, gilts (n = 6) were ovariectomized at 21, 24, 27, 30, or 34 hr after the onset of estrus; follicular fluids were aspirated; and each oocyte was stained and evaluated for cytogenetic stage of meiotic maturation. Inhibin was determined in diluted follicular fluids with a radioimmunoassay based on a synthetic peptide replica of part of the alpha subunit of porcine inhibin. Inhibin values were expressed in terms of thousands of units (kU) of a World Health Organization inhibin standard (86/690). Concentration of inhibin did not vary among hours (overall mean 248 kU/ml). Total follicular content of inhibin also was not different among hours (overall mean 57 kU/follicle). When follicles were classified on the basis of the maturation of the oocyte, significant differences were found. Concentration of inhibin in follicles with a germinal vesicle-stage oocyte was 138 kU/ml, whereas follicles with more mature oocytes had concentrations of between 204 and 254 kU/ml. Follicular content of inhibin showed a similar pattern with 34.9 kU/follicle at germinal vesicle stage, increasing to 42.5-56.1 kU/follicle at later stages. Quantities of inhibin were also negatively skewed and were positively correlated to follicular content of estradiol and dermatan sulfate.
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The concentration and content of inhibin was determined in individual porcine follicles from gilts ovariectomized at various times after the onset of estrus. In one experiment, gilts (n = 5) were ovariectomized at 0, 10, or 20 hr after the onset of estrus and the follicular fluids from all large follicles individually aspirated. In a second experiment, gilts (n = 6) were ovariectomized at 21, 24, 27, 30, or 34 hr after the onset of estrus; follicular fluids were aspirated; and each oocyte was stained and evaluated for cytogenetic stage of meiotic maturation. Inhibin was determined in diluted follicular fluids with a radioimmunoassay based on a synthetic peptide replica of part of the alpha subunit of porcine inhibin. Inhibin values were expressed in terms of thousands of units (kU) of a World Health Organization inhibin standard (86/690). Concentration of inhibin did not vary among hours (overall mean 248 kU/ml). Total follicular content of inhibin also was not different among hours (overall mean 57 kU/follicle). When follicles were classified on the basis of the maturation of the oocyte, significant differences were found. Concentration of inhibin in follicles with a germinal vesicle-stage oocyte was 138 kU/ml, whereas follicles with more mature oocytes had concentrations of between 204 and 254 kU/ml. Follicular content of inhibin showed a similar pattern with 34.9 kU/follicle at germinal vesicle stage, increasing to 42.5-56.1 kU/follicle at later stages. Quantities of inhibin were also negatively skewed and were positively correlated to follicular content of estradiol and dermatan sulfate.
Key concepts: Biology, Oocyte, Meiosis, Follicular fluid, Follicle, Andrology, Follicular phase, Ovarian follicle