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Brain Development: Normal Processes and the Effects of Alcohol ...

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10<br />

Prenatal Ethanol Exposure<br />

<strong>and</strong> Fetal Programming:<br />

Implications for Endocrine<br />

<strong>and</strong> Immune <strong>Development</strong><br />

<strong>and</strong> Long-Term Health<br />

Ethanol use <strong>and</strong> abuse result in clinical abnormalities<br />

<strong>of</strong> endocrin e functio n an d neuroendocrin e regula -<br />

tion (Morgan, 1982 ; Adler, 1992). Direct <strong>and</strong> indirect<br />

effects o f ethanol o n man y hormone systems , including<br />

th e adrenal , gonadal, <strong>and</strong> thyroi d axes, as well as<br />

on aldosterone , growt h hormone , parathyroi d hor -<br />

mone, calcitonin , insulin , <strong>and</strong> glucagon , hav e been<br />

reported. Secondar y complications suc h a s liver disease,<br />

malnutrition , <strong>and</strong> o<strong>the</strong> r medica l condition s <strong>of</strong>ten<br />

presen t i n alcoholic s ma y i n an d o f <strong>the</strong>mselves<br />

have endocrine consequences an d can potentially exacerbate<br />

<strong>the</strong> adverse effects o f ethanol.<br />

Whe<strong>the</strong>r ethanol-induce d endocrin e imbalance s<br />

contribute t o th e etiolog y o f fetal alcoho l spectru m<br />

disorders (FASD) is unknown, but i t is certainly a possibility<br />

(Anderson , 1981) . Th e effect s o f ethanol o n<br />

interactions betwee n th e pregnan t femal e an d fetu s<br />

are comple x (Rudee n an d Taylor , 1992 ; Weinberg ,<br />

1993a, 1993b , 1994) , <strong>and</strong> bot h direc t <strong>and</strong> indirec t effects<br />

o f ethanol o n feta l developmen t occur . Ethano l<br />

readily crosse s th e placenta , thu s directl y affectin g<br />

Joanna H. Sliwowska<br />

Xingqi Zhang<br />

Joanne Weinberg<br />

153<br />

developing fetal cell s <strong>and</strong> tissues , including those re -<br />

lated t o endocrin e function . I n addition , ethanol -<br />

induced change s i n endocrin e functio n ca n disrup t<br />

<strong>the</strong> hormona l interaction s betwee n th e pregnan t female<br />

<strong>and</strong> feta l systems , altering <strong>the</strong> normal hormon e<br />

balance an d indirectl y affecting th e developmen t <strong>of</strong><br />

fetal metabolic , physiological , an d endocrin e func -<br />

tions. Ethanol-induce d change s i n metaboli c <strong>and</strong>/o r<br />

endocrine function can also affect a female's ability to<br />

maintain a successful pregnancy , resulting in miscarriage<br />

or , i f <strong>the</strong> fetu s i s carried to term, possible con -<br />

genital defects. Of particular relevance to <strong>the</strong> present<br />

Chapter i s <strong>the</strong> notio n tha t disturbances <strong>of</strong> <strong>the</strong> recip -<br />

rocal interconnection s betwee n (a ) th e pregnan t<br />

female an d fetu s o r (b ) th e materna l an d neona -<br />

tal hypothalamic-pituitary-adrena l (HPA ) axes, ma y<br />

provide a common pathway by which perinatal exposure<br />

t o differen t agent s results in feta l programmin g<br />

(Angelucci e t al. , 1985) . Fetal o r early programming<br />

refers to <strong>the</strong> concept that early environmental or nongenetic<br />

factors , includin g pre- o r perinatal exposur e

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