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Published on: January 20, 2013
Endocrine studies in anencephaly
Insights
Anencephalic neonates show deficient hypothalamic-pituitary function but can release growth hormone and thyrotropin when directly stimulated. Prolactin levels were normal, suggesting autonomous pituitary function in some cases.
Area of Science:
- Endocrinology
- Neonatal Physiology
- Neuroscience
Background:
- Anencephaly is characterized by the absence of cortical and hypothalamic tissue and pituitary hypoplasia.
- Understanding the endocrine function in anencephaly is crucial for assessing pituitary and hypothalamic roles.
Purpose of the Study:
- To investigate the endocrine function in anencephalic neonates.
- To determine the influence of absent cortical and hypothalamic tissue on pituitary function.
- To assess the pituitary's capacity for hormone release in the absence of hypothalamic control.
Main Methods:
- Studied endocrine function in four anencephalic neonates.
- Administered intravenous glucose and insulin tolerance tests.
- Stimulated growth hormone release with lysine-vasopressin.
- Measured serum thyrotropin and prolactin levels after stimulation with releasing hormones.
Main Results:
- Anencephalic neonates exhibited higher peak blood sugar and faster glucose disposal rates.
- Insulin tolerance tests did not elevate plasma growth hormone and showed insulin resistance.
- Lysine-vasopressin and thyrotropin-releasing hormone stimulated growth hormone and thyrotropin release, respectively.
- Basal thyrotropin and growth hormone levels were low, but prolactin levels were normal.
Conclusions:
- Anterior pituitary function mediated by the hypothalamus is deficient in anencephaly.
- The anterior pituitary can release growth hormone and thyrotropin upon direct stimulation.
- Thyrotropin release may function autonomously, independent of hypothalamic control.
- Normal prolactin levels suggest the absence of hypothalamic prolactin inhibitory factor.
Abstract:
Endocrine function has been investigated in four anencephalic neonates to determine the influence of absence of cortical and hypothalamic tissue and of hypoplasia of the pituitary. Intravenous glucose administration resulted in higher peak values for blood sugar and more rapid glucose disposal rates than reported in normals. Intravenous insulin tolerance tests on two of the infants failed to evoke elevations in plasma growth hormone, and the infants showed a remarkable resistance to the hypoglycemic effect of insulin. Administration of lysine-vasopressin caused an active growth hormone release. Similarly, there was a large increase in serum thyrotropin after administration of synthetic thyrotropin-releasing hormone. Basal levels of both thyrotropin and growth hormone were low as compared with values reported for normal newborns. Prolactin values obtained on three of the infants were in the normal range. The results strongly suggest that anterior pituitary function mediated by the hypothalamus and its releasing factors is deficient in anencephaly. However, the anterior pituitary can release growth hormone and thyrotropin when stimulated directly and, in the case of thyrotropin release, may function autonomously. The normal prolactin values presumably reflect the absence of the hypothalamic prolactin inhibitory factor.
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