Exposure of a fetus to ethanol can lead to development of fetal alcohol syndrome, which is characterized by various morphological and behavioral deficits in fetal alcohol-exposed offspring. These offspring often show abnormalities in stress responses. Recent studies have revealed a possibility that the stress response anomalies seen in the FAE offspring are related to the functional abnormalities of hypothalamic beta-endorphin- (b-EP) producing neurons. However, there is not sufficient information available on the effect of ethanol on b-endorphin neuronal growth and differentiation. The present proposal will address this issue by studying the in vivo and in vitro effects of ethanol on beta-endorphin neuron growth and differentiation using rat as an animal model. The proposed research will test the hypotheses that ethanol exposure during the developmental period induces programmed cell death in b-EP neurons and that cAMP and transforming growth factor-beta1 (TGF-beta1) may be involved in controlling the ethanol-induced neurotoxicity. Specific objectives of this proposal are to: 1) determine the action of ethanol on b-EP neuronal growth and differentiation and the consequence on the development of the functional b-EP neurons, 2) identify the role of the cAMP system in ethanol neurotoxic action on b-EP neurons, 3) evaluate the role of TGF-beta in ethanol neurotoxic action on b-EP neurons, 4) study the signaling mechanisms of the ethanol neurotoxic action on b-EP neurons. Ethanol's action on programmed cell death in the b-EP neurons will be studied both in vivo and in vitro using biochemical and immunocytochemical techniques. The mechanism of ethanol's neurotoxic action on b-EP neurons will be determined using a rat fetal hypothalamic neuronal cell culture system. Two-pronged approaches will be applied to study the mechanisms of the ethanol neurotoxic action; one to pharmacologically manipulate the signal transduction systems, another to measure the intracellular level of these signal transducers by histological, biochemical and molecular techniques.

Agency
National Institute of Health (NIH)
Institute
National Institute on Alcohol Abuse and Alcoholism (NIAAA)
Type
Research Project (R01)
Project #
5R01AA008757-12
Application #
6771074
Study Section
Alcohol and Toxicology Subcommittee 4 (ALTX)
Program Officer
Sorensen, Roger
Project Start
1991-08-01
Project End
2006-06-30
Budget Start
2004-07-01
Budget End
2006-06-30
Support Year
12
Fiscal Year
2004
Total Cost
$296,297
Indirect Cost
Name
Rutgers University
Department
Type
Organized Research Units
DUNS #
001912864
City
New Brunswick
State
NJ
Country
United States
Zip Code
08901
Chastain, Lucy G; Sarkar, Dipak K (2017) Alcohol effects on the epigenome in the germline: Role in the inheritance of alcohol-related pathology. Alcohol 60:53-66
Sarkar, Dipak K (2016) Male germline transmits fetal alcohol epigenetic marks for multiple generations: a review. Addict Biol 21:23-34
Zhang, Changqing; Franklin, Tina; Sarkar, Dipak K (2016) Inhibition of Mammary Cancer Progression in Fetal Alcohol Exposed Rats by ?-Endorphin Neurons. Alcohol Clin Exp Res 40:134-40
Logan, Ryan W; Wynne, Olivia; Maglakelidze, George et al. (2015) ?-Endorphin neuronal transplantation into the hypothalamus alters anxiety-like behaviors in prenatal alcohol-exposed rats and alcohol-non-preferring and alcohol-preferring rats. Alcohol Clin Exp Res 39:146-57
Logan, Ryan W; Zhang, Changqing; Murugan, Sengottuvelan et al. (2012) Chronic shift-lag alters the circadian clock of NK cells and promotes lung cancer growth in rats. J Immunol 188:2583-91
Agapito, Maria; Mian, Nadia; Boyadjieva, Nadka I et al. (2010) Period 2 gene deletion abolishes beta-endorphin neuronal response to ethanol. Alcohol Clin Exp Res 34:1613-8
Sarkar, Dipak K; Boyadjieva, Nadka I; Chen, Cui Ping et al. (2008) Cyclic adenosine monophosphate differentiated beta-endorphin neurons promote immune function and prevent prostate cancer growth. Proc Natl Acad Sci U S A 105:9105-10
Kuhn, Peter; Sarkar, Dipak K (2008) Ethanol induces apoptotic death of beta-endorphin neurons in the rat hypothalamus by a TGF-beta 1-dependent mechanism. Alcohol Clin Exp Res 32:706-14
Arjona, Alvaro; Sarkar, Dipak K (2008) Are circadian rhythms the code of hypothalamic-immune communication? Insights from natural killer cells. Neurochem Res 33:708-18
Sarkar, Dipak K; Kuhn, Peter; Marano, Jasson et al. (2007) Alcohol exposure during the developmental period induces beta-endorphin neuronal death and causes alteration in the opioid control of stress axis function. Endocrinology 148:2828-34

Showing the most recent 10 out of 36 publications