Literature DB >> 2736078

Arginine vasopressin and body fluid homeostasis in the fetal alcohol exposed rat.

D L Dow-Edwards1, H Trachtman, E P Riley, L A Freed, T H Milhorat.   

Abstract

Studies involving fluid homeostasis were carried out in adult Long-Evans rats born to mothers given liquid diets containing 35% of the calories derived from ethanol and compared to offspring of dams given isocaloric liquid diets containing no ethanol. Plasma levels of arginine vasopressin (AVP), plasma and urine osmolality, and urine production were determined in water-sated and water-deprived offspring. In the water-sated condition, the group exposed to alcohol prenatally had plasma levels of AVP seven-fold above control levels. This increase was associated with a large increase in within-group variability. Water consumption was also significantly elevated in the group of fetal alcohol exposed (FAE) rats. Plasma and urine osmolality and urine production were similar to control levels. In the control animals, 24-hr of water deprivation produced the expected increase in AVP, in plasma and urine osmolality, and decrease in urine production. The FAE animals, however, showed parallel changes in plasma and urine osmolality and urine production with no significant change in AVP. Examination of basal glucose metabolic rates in the cerebral structures involved in fluid homeostasis revealed that despite the large increase in AVP levels in the FAE rats, only the neurohypophysis and supraoptic nuclei showed significant increases in activity. These data suggest that fetal alcohol exposure causes a long-term disruption in the central mechanisms regulating vasopressin release and fluid homeostatic responses.

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Year:  1989        PMID: 2736078     DOI: 10.1016/0741-8329(89)90018-9

Source DB:  PubMed          Journal:  Alcohol        ISSN: 0741-8329            Impact factor:   2.405


  5 in total

Review 1.  Vascular effects of maternal alcohol consumption.

Authors:  Jayanth Ramadoss; Ronald R Magness
Journal:  Am J Physiol Heart Circ Physiol       Date:  2012-06-22       Impact factor: 4.733

2.  Prolonged ethanol ingestion increases renal AQP2 and AQP3 expression in adult rats and in their offspring.

Authors:  M García-Delgado; M J Peral; O García-Benítez; O Carreras; A A Ilundáin
Journal:  J Membr Biol       Date:  2004-03-15       Impact factor: 1.843

3.  Pituitary lacks sexual dimorphism and displays reduced signal intensity on T1-weighted MRI in adolescents with histories of heavy prenatal alcohol exposure.

Authors:  Eileen M Moore; M Alejandra Infante; Robyn Migliorini; Sarah N Mattson; Edward P Riley
Journal:  Neurotoxicol Teratol       Date:  2016-09-09       Impact factor: 3.763

4.  Effects of prenatal ethanol exposure and sex on the arginine vasopressin response to hemorrhage in the rat.

Authors:  Danielle N Bird; Aileen K Sato; Daniel S Knee; Catherine F T Uyehara; Donald A Person; John R Claybaugh
Journal:  Am J Physiol Regul Integr Comp Physiol       Date:  2006-07       Impact factor: 3.619

5.  Periconceptional ethanol exposure induces a sex specific diuresis and increase in AQP2 and AVPR2 in the kidneys of aged rat offspring.

Authors:  Emily S Dorey; Sarah L Walton; Jacinta I Kalisch-Smith; Tamara M Paravicini; Emelie M Gardebjer; Kristy A Weir; Reetu R Singh; Helle Bielefeldt-Ohmann; Stephen T Anderson; Mary E Wlodek; Karen M Moritz
Journal:  Physiol Rep       Date:  2019-11
  5 in total

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