Maternal stress alters endocrine function ...
Type de document :
Article dans une revue scientifique: Article original
PMID :
URL permanente :
Titre :
Maternal stress alters endocrine function of the feto-placental unit in rats.
Auteur(s) :
Mairesse, Jérôme [Auteur]
Lesage, Jean [Auteur]
Breton, Christophe [Auteur]
Bréant, Bernadette [Auteur]
Hahn, Tom [Auteur]
Darnaudéry, Muriel [Auteur]
Dickson, Suzanne L [Auteur]
Seckl, Jonathan [Auteur]
Blondeau, Bertrand [Auteur]
Vieau, didier [Auteur]
Maccari, Stefania [Auteur]
Viltart, Odile [Auteur]
Institut Pasteur de Lille
Lesage, Jean [Auteur]

Breton, Christophe [Auteur]

Bréant, Bernadette [Auteur]
Hahn, Tom [Auteur]
Darnaudéry, Muriel [Auteur]
Dickson, Suzanne L [Auteur]
Seckl, Jonathan [Auteur]
Blondeau, Bertrand [Auteur]
Vieau, didier [Auteur]

Maccari, Stefania [Auteur]

Viltart, Odile [Auteur]

Institut Pasteur de Lille
Titre de la revue :
American journal of physiology. Endocrinology and metabolism
Nom court de la revue :
Am J Physiol Endocrinol Metab
Numéro :
292
Pagination :
E1526-33
Date de publication :
2007-06-01
ISSN :
0193-1849
Mot(s)-clé(s) en anglais :
11-beta-Hydroxysteroid Dehydrogenase Type 2
Adrenal Glands
Animals
Blood Glucose
Body Weight
Chronic Disease
Eating
Endocrine Glands
Female
Fetal Blood
Fetus
Glucose Transport Proteins, Facilitative
Hormones
Insulin-Secreting Cells
Islets of Langerhans
Male
Organ Size
Pancreas
Placenta
Pregnancy
Pregnancy Complications
Rats
Restraint, Physical
Stress, Physiological
Testis
Adrenal Glands
Animals
Blood Glucose
Body Weight
Chronic Disease
Eating
Endocrine Glands
Female
Fetal Blood
Fetus
Glucose Transport Proteins, Facilitative
Hormones
Insulin-Secreting Cells
Islets of Langerhans
Male
Organ Size
Pancreas
Placenta
Pregnancy
Pregnancy Complications
Rats
Restraint, Physical
Stress, Physiological
Testis
Discipline(s) HAL :
Sciences cognitives
Résumé en anglais : [en]
Prenatal stress (PS) can cause early and long-term developmental effects resulting in part from altered maternal and/or fetal glucocorticoid exposure. The aim of the present study was to assess the impact of chronic restraint ...
Lire la suite >Prenatal stress (PS) can cause early and long-term developmental effects resulting in part from altered maternal and/or fetal glucocorticoid exposure. The aim of the present study was to assess the impact of chronic restraint stress during late gestation on feto-placental unit physiology and function in embryonic (E) day 21 male rat fetuses. Chronic stress decreased body weight gain and food intake of the dams and increased their adrenal weight. In the placenta of PS rats, the expression of glucose transporter type 1 (GLUT1) was decreased, whereas GLUT3 and GLUT4 were slightly increased. Moreover, placental expression and activity of the glucocorticoid "barrier" enzyme 11beta-hydroxysteroid dehydrogenase type 2 was strongly reduced. At E21, PS fetuses exhibited decreased body, adrenal pancreas, and testis weights. These alterations were associated with reduced pancreatic beta-cell mass, plasma levels of glucose, growth hormone, and ACTH, whereas corticosterone, insulin, IGF-1, and CBG levels were unaffected. These data emphasize the impact of PS on both fetal growth and endocrine function as well as on placental physiology, suggesting that PS could program processes implied in adult biology and pathophysiology.Lire moins >
Lire la suite >Prenatal stress (PS) can cause early and long-term developmental effects resulting in part from altered maternal and/or fetal glucocorticoid exposure. The aim of the present study was to assess the impact of chronic restraint stress during late gestation on feto-placental unit physiology and function in embryonic (E) day 21 male rat fetuses. Chronic stress decreased body weight gain and food intake of the dams and increased their adrenal weight. In the placenta of PS rats, the expression of glucose transporter type 1 (GLUT1) was decreased, whereas GLUT3 and GLUT4 were slightly increased. Moreover, placental expression and activity of the glucocorticoid "barrier" enzyme 11beta-hydroxysteroid dehydrogenase type 2 was strongly reduced. At E21, PS fetuses exhibited decreased body, adrenal pancreas, and testis weights. These alterations were associated with reduced pancreatic beta-cell mass, plasma levels of glucose, growth hormone, and ACTH, whereas corticosterone, insulin, IGF-1, and CBG levels were unaffected. These data emphasize the impact of PS on both fetal growth and endocrine function as well as on placental physiology, suggesting that PS could program processes implied in adult biology and pathophysiology.Lire moins >
Langue :
Anglais
Comité de lecture :
Oui
Audience :
Internationale
Vulgarisation :
Non
Établissement(s) :
Université de Lille
CNRS
CHU Lille
CNRS
CHU Lille
Collections :
Date de dépôt :
2024-01-12T14:37:03Z
2024-02-28T11:50:06Z
2024-02-28T11:50:06Z
Fichiers
- Mairesse et al. AJP 2007.pdf
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