Maternal hypothyroxinemia disrupts neurotransmitter metabolic enzymes in developing brain

• Published in: Journal of endocrinology Vol. 161; no. 2; pp. 273 - 279
• Main Authors: Evans, IM, Sinha, AK, Pickard, MR, Edwards, PR, Leonard, AJ, Ekins, RP
• Format: Journal Article Conference Proceeding
• Language: English
• Published: Colchester BioScientifica 01.05.1999; Portland Press
• Subjects: Aging - metabolism; Animals; Biological and medical sciences; Brain - embryology; Brain - enzymology; Choline O-Acetyltransferase - metabolism; Disease Models, Animal; Diseases of mother, fetus and pregnancy; Dopa Decarboxylase - metabolism; Female; Fetus - enzymology; Gynecology. Andrology. Obstetrics; Male; Medical sciences; Monoamine Oxidase - metabolism; Neurotransmitter Agents - metabolism; Pregnancy; Pregnancy Complications - blood; Pregnancy. Fetus. Placenta; Prenatal Exposure Delayed Effects; Rats; Rats, Sprague-Dawley; Thyroxine - blood; Thyroxine - deficiency; Endocrinopathy; Embryonic development; Rat; Rodentia; Central nervous system; Thyroid diseases; Biosynthesis; Hypothyroidism; Maternal diseases; Pregnancy; Vertebrata; Experimental disease; Mammalia; Enzymatic activity; Animal; Thyroxine; Neurotransmitter; Thyroid hormone; Brain (vertebrata)
• ISSN: 0022-0795; 1479-6805
• DOI: 10.1677/joe.0.1610273

Maternal thyroid status influences early brain development and, consequently, cognitive and motor function in humans and rats. The biochemical targets of maternal thyroid hormone (TH) action in fetal brain remain poorly defined. A partially thyroidectomized rat dam model was therefore used to investigate the influence of maternal hypothyroxinemia on the specific activities of cholinergic and monoaminergic neurotransmitter metabolic enzymes in the developing brain. Maternal hypothyroxinemia was associated with reduced monoamine oxidase (MAO) activity in fetal whole brain at 16 and 19 days gestation (dg). A similar trend was observed for choline acetyltransferase (ChAT) activity. In contrast, DOPA decarboxylase (DDC) activity was markedly elevated at 21 dg. Further study of these enzymes at 14 dg showed no differences between normal and experimental progeny - suggesting they become TH sensitive after this age. Tyrosine hydroxylase (TyrH) and acetylcholinesterase (AChE) activities were unaffected prenatally. During postnatal development, the activities of TyrH, MAO, DDC and, to a lesser extent, AChE were increased in a brain region- and age-specific manner in experimental progeny. The prenatal disturbances noted in this study may have wide-ranging consequences since they occur when neurotransmitters have putative neurotropic roles in brain development. Furthermore, the chronic disturbances in enzyme activity observed during postnatal life may affect neurotransmission, thereby contributing to the behavioural dysfunction seen in adult progeny of hypothyroxinemic dams.