Supplemental choline does not attenuate the effects of neonatal ethanol administration on habituation of the heart rate orienting response in rats

被引:6
作者
Hunt, Pamela S. [1 ]
Jacobson, Sarah E. [1 ]
Kim, Sarah [1 ]
机构
[1] Coll William & Mary, Dept Psychol, Williamsburg, VA 23187 USA
关键词
Dietary supplement; Choline; Fetal alcohol; Olfactory; Orienting; PRENATAL ALCOHOL EXPOSURE; BEHAVIORAL ALTERATIONS; SPECTRUM DISORDERS; DEFICITS; AVAILABILITY; GESTATION; REVERSAL; MEMORY; BIRTH; TRACE;
D O I
10.1016/j.ntt.2014.05.008
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Several studies using rodent subjects have now shown that extra dietary choline may prevent or even reverse the deleterious effects of pre- and early post-natal ethanol administration. Choline supplementation has been shown to attenuate many, although not all, of ethanol's effects on brain development and behavior. Our laboratory has consistently reported impaired habituation of the heart rate orienting response to a novel olfactory stimulus in animals exposed to ethanol on postnatal days (PD) 4-9. Here we examine whether supplemental choline given both during and after ethanol administration could alleviate these ethanol-induced deficits. Subjects were given 5 g/kg/day ethanol or sham intubations on PD 4-9. Half of the subjects in each group were given a single daily s.c. injection of choline chloride on PD 4-20, while the other half were injected daily with saline. Pups were tested for heart rate orienting and response habituation in a single test session on PD 23. Results replicated the ethanol-induced impairment in response habituation. However, choline supplementation had no effect on orienting or habituation in either neonatal treatment group. These findings indicate that habituation deficits induced by ethanol are not alleviated by extra dietary choline using these parameters. Choline holds great promise as a treatment for some fetal alcohol effects, but is not an effective treatment for all ethanol-related deficits. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:121 / 125
页数:5
相关论文
共 41 条
[1]  
[Anonymous], ATTENTION ORIENTING
[2]   Imprinting of hippocampal metabolism of choline by its availability during gestation: Implications for cholinergic neurotransmission [J].
Blusztajn, JK ;
Cermak, JM ;
Holler, T ;
Jackson, DA .
JOURNAL OF PHYSIOLOGY-PARIS, 1998, 92 (3-4) :199-203
[3]   Antioxidants and fetal protection against ethanol teratogenicity - I. Review of the experimental data and implications to humans [J].
Cohen-Kerem, R ;
Koren, G .
NEUROTOXICOLOGY AND TERATOLOGY, 2003, 25 (01) :1-9
[4]   Verbal and Nonverbal Memory in Adults Prenatally Exposed to Alcohol [J].
Coles, Claire D. ;
Lynch, Mary Ellen ;
Kable, Julie A. ;
Johnson, Katrina C. ;
Goldstein, Felicia C. .
ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH, 2010, 34 (05) :897-906
[5]   Inhibition of cholinergic muscarinic signaling by ethanol: Potential mechanism of developmental neurotoxicity and biological plausibility for the beneficial effects of choline supplementation [J].
Costa, Lucio G. ;
Giordano, Gennaro ;
Guizzetti, Marina .
INTERNATIONAL JOURNAL OF ALCOHOL AND DRUG RESEARCH, 2013, 2 (03) :17-25
[6]   Prenatal ethanol exposure and spatial navigation: Effects of postnatal handling and aging [J].
Gabriel, KI ;
Johnston, S ;
Weinberg, J .
DEVELOPMENTAL PSYCHOBIOLOGY, 2002, 40 (04) :345-357
[7]   Fetal alcohol spectrum disorders: new perspectives on diagnosis and intervention [J].
Goodlett, Charles R. .
ALCOHOL, 2010, 44 (7-8) :579-582
[8]   Neonatal binge ethanol exposure using intubation: Timing and dose effects on place learning [J].
Goodlett, CR ;
Johnson, TB .
NEUROTOXICOLOGY AND TERATOLOGY, 1997, 19 (06) :435-446
[9]   Fetal alcohol effects:: Potential treatments from basic science [J].
Guerri, C ;
Pascual, M ;
García-Minguillán, MC ;
Charness, ME ;
Wilkemeyer, MF ;
Klintsova, AY ;
Goodlett, CR ;
Greenough, WT ;
Sakata-Haga, H ;
Dominguez, HD ;
Thomas, JD .
ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH, 2005, 29 (06) :1074-1079
[10]   Differential habituation to repeated sounds in infants at high risk for autism [J].
Guiraud, Jeanne A. ;
Kushnerenko, Elena ;
Tomalski, Przemyslaw ;
Davies, Kim ;
Ribeiro, Helena ;
Johnson, Mark H. .
NEUROREPORT, 2011, 22 (16) :845-849