Prenatal sex determination by Y-fluorescence of amniotic fluid interphase nuclei.
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Biomedical subjects
Publications and source records attributed to V Hingorani.
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The blast transformation of peripheral leukocytes from pregnant and nonpregnant women has been studied at different time intervals with graded concentrations of phytohemagglutinin. The transformation is markedly depressed during pregnancy. Leukocytes from nonpregnant women and men show diminished transformation when cultured in a medium containing plasma from pregnant women.
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In vitro biosynthesis of oestrogens in microsomal and 10,000 g supernatant fractions of placentae, ten each, from normal and toxaemic pregnancies has been investigated. Dehydroepiandrosterone sulphate (DHAS), dehydroepiandrosterone (DHA) and androstenedione were used as substrates and their conversion to oestrone and oestradiol studied. In all the placental preparations the relative efficiency of the conversion of these androgens to oestrogens, though differing greatly between subcellular fractions as well as between normal and toxaemic placentae, was invariably in the order of DHAS greater than DHA greater than androstenedione. The conversion of these androgen precursors to oestrone and oestradiol was reduced in toxaemia compared with the normal placenta. Moreover, formation of oestradiol was much more reduced than that of oestrone. The free oestradiol level in the serum was also found to be lower in toxaemic pregnancies as compared with the normal range. The inter-conversions of oestrogens further showed a significantly reduced conversion of oestrone to oestradiol in toxaemic placentae compared with normal placentae. The results may explain the lowered blood oestradiol levels observed in toxaemia of pregnancy and thus provide an explanation of the usefulness of the estimation of the oestradiol level as an index of feto-placental function.
A study of the metabolism of oestradiol in the human endometrium and myometrium of the proliferative and secretory phases of the cycle showed that the conversion of oestradiol to oestrone by endometrium in the proliferative phase was higher than that in the secretory phase. The decreased metabolic activity of the secretory phase endometrium was attributed to the influence of progesterone on the endometrium. The metabolic conversion of oestradiol to oestrone was enhanced when pyridine nucleotides were added to the system. The conversion of oestradiol to oestrone was maximum in the cytoplasmic and nuclear fractions of the endometrium. Furthermore, the conversion of oestradiol was low in all the subcellular fractions of the myometrium as compared with the endometrial subcellular fractions. The presence of co-factors increased the metabolic conversion of oestradiol to oestrone in the subcellular fractions of the endometrium. The presence of 17 beta-hydroxysteroid oxidoreductase was indicated in all the subcellular fractions. A correlation was found between the amount of oestradiol and oestrone bound to the receptors in the uterus and the rate of metabolism of oestradiol in the uterus. The physiological significance of metabolism of oestradiol and the hormone action are discussed.
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