Literature DB >> 14506413

Effect of duration of alcohol consumption on calcium and bone metabolism during pregnancy in the rat.

Kathy Keiver1, Joanne Weinberg.   

Abstract

BACKGROUND: Little is known about the consequences of drinking during pregnancy for the long-term health of the mother. Alcohol (ethanol) has been shown to disrupt calcium (Ca) homeostasis and is known to have deleterious effects on bone. During pregnancy, bone turnover is increased to maintain Ca homeostasis; therefore, pregnancy may be a time of life when maternal bone is particularly susceptible to the effects of ethanol. This study investigated the effect of duration of ethanol consumption on Ca homeostasis and bone during pregnancy in the rat.
METHODS: Rats were fed ethanol (36% ethanol-derived calories) in liquid diets for 3 (21 days gestation only) or 6 (3 weeks before and throughout 21 days gestation) weeks. Maternal blood was analyzed for Ca (total and ionized Ca [iCa]), the Ca-regulating hormones (parathyroid hormone [PTH], 1,25(OH)2D, calcitonin), and osteocalcin (a marker for bone formation). Bone was analyzed for ash (mineral) content.
RESULTS: Dams consuming ethanol (E dams) had decreased blood Ca levels (total and iCa) at both 3 and 6 weeks, but iCa was lower in E dams after 6 compared with 3 weeks. Importantly, ethanol seemed to interfere with the normal compensatory response to these decreased Ca levels. In contrast to pair-fed controls, serum PTH levels actually were decreased, 1,25(OH)2D levels failed to increase, and calcitonin levels were increased in ethanol-consuming dams, regardless of duration. Moreover, ethanol decreased bone formation, as indicated by serum osteocalcin levels, after both 3 and 6 weeks consumption, and after 6 weeks, the ash content of bone also was decreased. In addition, a relationship was found between the blood alcohol concentration (BAC) and some measures of Ca and bone metabolism. Serum 1,25(OH)2D and osteocalcin levels varied inversely, whereas serum calcitonin varied directly with BAC, suggesting that time of sampling after drinking may be an important variable for interpreting ethanol's effects on Ca and bone metabolism. In all rats, serum osteocalcin levels varied directly with PTH and 1,25(OH)2D levels.
CONCLUSIONS: Ethanol consumption during pregnancy impaired Ca homeostasis in the dam, regardless of duration of consumption, and resulted in decreased bone formation and ash content of bone. Significant relationships among the Ca-regulating hormones, BAC, and osteocalcin support the hypothesis that ethanol's effects on the Ca-regulating hormones may mediate some of its effects on bone.

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Year:  2003        PMID: 14506413     DOI: 10.1097/01.ALC.0000086063.71754.C1

Source DB:  PubMed          Journal:  Alcohol Clin Exp Res        ISSN: 0145-6008            Impact factor:   3.455


  5 in total

1.  Effects of prenatal ethanol exposure on regulation of basal hypothalamic-pituitary-adrenal activity and hippocampal 5-HT1A receptor mRNA levels in female rats across the estrous cycle.

Authors:  J H Sliwowska; N Lan; F Yamashita; A G Halpert; V Viau; J Weinberg
Journal:  Psychoneuroendocrinology       Date:  2008-07-30       Impact factor: 4.905

2.  Chronic ethanol consumption leads to disruption of vitamin D3 homeostasis associated with induction of renal 1,25 dihydroxyvitamin D3-24-hydroxylase (CYP24A1).

Authors:  Kartik Shankar; Xiaoli Liu; Rohit Singhal; Jin-Ran Chen; Shanmugam Nagarajan; Thomas M Badger; Martin J J Ronis
Journal:  Endocrinology       Date:  2007-12-27       Impact factor: 4.736

3.  Prenatal ethanol exposure disrupts the histological stages of fetal bone development.

Authors:  M E Snow; K Keiver
Journal:  Bone       Date:  2007-04-25       Impact factor: 4.398

4.  The role of acidemia in maternal binge alcohol-induced alterations in fetal bone functional properties.

Authors:  Onkar B Sawant; Jayanth Ramadoss; Harry A Hogan; Shannon E Washburn
Journal:  Alcohol Clin Exp Res       Date:  2013-05-03       Impact factor: 3.455

5.  Impact of Alcohol on Bone Health, Homeostasis and Fracture repair.

Authors:  Jonathan M Eby; Farah Sharieh; John J Callaci
Journal:  Curr Pathobiol Rep       Date:  2020-07-28
  5 in total

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