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The physiological importance of and therapeutic interest in dehydroepiandrosterone (DHEA) has been predominantly in relation to its action as an inhibitor of the promotion and progression of several kinds of tumours, including those of breast, prostate, lung, colon, liver and skin tissues. The aim of the present study was to determine the role of DHEA in diethylstilboestrol (DES)-induced pituitary hyperplasia. Female Sprague-Dawley rats were divided into four treatment groups: DES (implanted s.c. with a 20 mg DES pellet), DHEA (two 50 mg DHEA pellets), DHEA/DES (both DHEA and DES pellets), and controls (not implanted). Every week, all rats were weighed and cycled, and jugular blood samples were obtained. After 7 weeks, rats were killed. Hypophyses were removed and weighed, and serum prolactin, GH, IGF-I and leptin levels were assayed by RIA. DHEA cotreatment reduced pituitary enlargement by 39% in DES-treated rats. It also reduced the hyperprolactinaemia (280.4+/-43.6 ng/ml for DHEA/DES vs 823.5+/- 127.1 ng/ml for DES) and partially reversed the loss of body weight induced by DES. DHEA treatment did not modify the effects of DES on serum GH, IGF-I and leptin levels. But DHEA per se also increased pituitary weight and induced hyperprolactinaemia, although to a lesser degree than DES. We conclude that DHEA administration has beneficial effects on oestrogen-induced pituitary hyperplasia and hyperprolactinaemia, but the fact that DHEA per se also induces diverse hormonal effects and a slight pituitary enlargement limits its use as a possible therapeutic drug.
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Endocrine Signalling Group, Barts and the London School of Medicine and Dentistry, Department of Medicine, Cardiovascular and Inflammation Group, Laboratory for Integrated Neurosciences and Endocrinology, Veterinary Basic Sciences, Royal Veterinary College, University of London, Royal College Street, London NW1 0TU, UK
Endocrine Signalling Group, Barts and the London School of Medicine and Dentistry, Department of Medicine, Cardiovascular and Inflammation Group, Laboratory for Integrated Neurosciences and Endocrinology, Veterinary Basic Sciences, Royal Veterinary College, University of London, Royal College Street, London NW1 0TU, UK
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lethality ( Chusho et al . 2001 ), but investigation of their neuroendocrine tissues has not been reported. Early studies characterising the expression profile of CNP suggested that the CNS and anterior pituitary are rich sources of CNP ( Sudoh et al
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sepsis in patients, allowing differentiation between patients with systemic inflammatory response syndrome and patients with sepsis ( Yousef et al . 2010 ). The hypothalamic–pituitary–adrenal (HPA) axis plays an important protective role in the body
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Introduction Maintaining homeostasis in a constantly changing environment is a fundamental process of life. Hans Selye, the father of the stress concept, defined the hypothalamic–pituitary–adrenocortical (HPA) axis as the major component required
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Sackler School of Graduate Biomedical Sciences, Departments of Developmental, Integrated Physiology and Pathobiology, Molecular and Chemical Biology
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Sackler School of Graduate Biomedical Sciences, Departments of Developmental, Integrated Physiology and Pathobiology, Molecular and Chemical Biology
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Introduction The hypothalamic–pituitary–adrenal (HPA) axis plays a vital role in restoring homeostasis following environmental challenge. Physical or psychological stress results in cortisol production in humans or corticosterone (CORT) in rodents
Department of Ophthalmology, University of Tennessee Health Science Center, 930 Madison Avenue, RM525, Memphis, Tennessee 38163, USA
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Department of Ophthalmology, University of Tennessee Health Science Center, 930 Madison Avenue, RM525, Memphis, Tennessee 38163, USA
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Department of Ophthalmology, University of Tennessee Health Science Center, 930 Madison Avenue, RM525, Memphis, Tennessee 38163, USA
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Introduction Corticotropin-releasing factor (CRF) is the most proximal element of the hypothalamic–pituitary–adrenal (HPA) axis, a system that coordinates the body response to systemic stress ( Selye 1936 , Vale et al. 1981
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Introduction Vasopressin (arginine vasopressin, AVP) and CRH are the two main neuropeptides regulating the hypothalamic–pituitary–adrenal (HPA) axis. AVP is a nonapeptide synthesised in parvocellular neurons of the paraventricular nucleus (PVN) of
INRA, Laboratory of Nutrition and Integrative Neurobiology, INSERM, Nutrition and Integrative Neurobiology, UMR1286, Université de Bordeaux 2, 146, rue Léo Saignat, 33076 Bordeaux Cedex, France
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INRA, Laboratory of Nutrition and Integrative Neurobiology, INSERM, Nutrition and Integrative Neurobiology, UMR1286, Université de Bordeaux 2, 146, rue Léo Saignat, 33076 Bordeaux Cedex, France
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INRA, Laboratory of Nutrition and Integrative Neurobiology, INSERM, Nutrition and Integrative Neurobiology, UMR1286, Université de Bordeaux 2, 146, rue Léo Saignat, 33076 Bordeaux Cedex, France
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INRA, Laboratory of Nutrition and Integrative Neurobiology, INSERM, Nutrition and Integrative Neurobiology, UMR1286, Université de Bordeaux 2, 146, rue Léo Saignat, 33076 Bordeaux Cedex, France
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brain-derived neurotrophic factor ( Brossaud et al . 2013 ), only a few studies have explored the regulation of hypothalamic–pituitary–adrenal (HPA) axis function by retinoids. Previous studies have suggested an inhibition of glucocorticoid synthesis
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Introduction The classic response to chronic stress consists of an elegant, concerted interplay of two important pathways, the sympathetic nervous system (SNS) and the hypothalamus–pituitary–adrenal axis (HPA). The chronic activation of these stress
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in animals ( Levin et al . 1997 ). A key process involved in this variability lies in the responsivity of the hypothalamic–pituitary–adrenocortical (HPA) axis. Indeed, corticosteroid hormones are implicated in nutritional regulations 1) by their