The effects of alcohol and cannabinoid exposure during the brain growth spurt on behavioral development in rats

被引:23
作者
Breit, Kristen R. [1 ]
Zamudio, Brandonn [1 ]
Thomas, Jennifer D. [1 ]
机构
[1] San Diego State Univ, Dept Psychol, Ctr Behav Teratol, 6330 Alvarado Ct,Suite 100, San Diego, CA 92120 USA
来源
BIRTH DEFECTS RESEARCH | 2019年 / 111卷 / 12期
关键词
behavior; cannabinoid; development; ethanol; teratology; RECEPTOR AGONIST SPIRADOLINE; PRENATAL MARIJUANA USE; SEX-DIFFERENCES; SPECTRUM DISORDERS; ETHANOL EXPOSURE; FOLLOW-UP; PERINATAL EXPOSURE; GENE-EXPRESSION; WORKING-MEMORY; ADULT-RATS;
D O I
10.1002/bdr2.1487
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Cannabis is the most commonly used illicit drug among pregnant women. Moreover, over half of pregnant women who are consuming cannabis are also consuming alcohol; however, the consequences of combined prenatal alcohol and cannabis exposure on fetal development are not well understood. The current study examined behavioral development following exposure to ethanol (EtOH) and/or CP-55,940 (CP), a cannabinoid receptor agonist. From postnatal days (PD) 4-9, a period of brain development equivalent to the third trimester, Sprague-Dawley rats received EtOH (5.25 g/kg/day) or sham intubation, as well as CP (0.4 mg/kg/day) or vehicle. All subjects were tested on open field activity (PD 18-21), elevated plus maze (PD 25), and spatial learning (PD 40-46) tasks. Both EtOH and CP increased locomotor activity in the open field, and the combination produced more severe overactivity than either exposure alone. Similarly, increases in thigmotaxis in the Morris water maze were caused by either EtOH or CP alone, and were more severe with combined exposure, although only EtOH impaired spatial learning. Finally, developmental CP significantly increased time spent in the open arms on the elevated plus maze. Overall, these data indicate that EtOH and CP produce some independent effects on behavior, and that the combination produces more severe overactivity in the open field. Importantly, these data suggest that prenatal cannabis disrupts development and combined prenatal exposure to alcohol and cannabis may be particularly damaging to the developing fetus, which has implications for the lives of affected individuals and families and also for establishing public health policy.
引用
收藏
页码:760 / 774
页数:15
相关论文
共 119 条
[1]  
Abel E.L., 1986, HDB BEHAV TERATOLOGY, DOI [10.1007/978-1-4613-2189-7_12, DOI 10.1007/978-1-4613-2189-7_12]
[2]   EFFECTS OF LOW-DOSES OF ALCOHOL ON DELTA-9-TETRAHYDROCANNABINOLS EFFECTS IN PREGNANT RATS [J].
ABEL, EL ;
SUBRAMANIAN, MG .
LIFE SCIENCES, 1990, 47 (18) :1677-1682
[3]   EFFECTS OF DELTA-9-TETRAHYDROCANNABINOL, PHENOBARBITAL, AND THEIR COMBINATION ON PREGNANCY AND OFFSPRING IN RATS [J].
ABEL, EL ;
TAN, SE ;
SUBRAMANIAN, M .
TERATOLOGY, 1987, 36 (02) :193-198
[4]  
[Anonymous], 2017, NY TIMES
[5]  
Barnett S.A., 1963, RAT STUDY BEHAV
[6]   EFFECTS OF PRENATAL ALCOHOL EXPOSURE ON THE SEXUALLY DIMORPHIC NUCLEUS OF THE PREOPTIC AREA OF THE HYPOTHALAMUS IN MALE AND FEMALE RATS [J].
BARRON, S ;
TIEMAN, SB ;
RILEY, EP .
ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH, 1988, 12 (01) :59-64
[7]   Acute ethanol suppresses glutamatergic neurotransmission through endocannabinoids in hippocampal neurons [J].
Basavarajappa, Balapal S. ;
Ninan, Ipe ;
Arancio, Ottavio .
JOURNAL OF NEUROCHEMISTRY, 2008, 107 (04) :1001-1013
[8]   Fetal Alcohol Spectrum Disorder: Potential Role of Endocannabinoids Signaling [J].
Basavarajappa, Balapal S. .
BRAIN SCIENCES, 2015, 5 (04) :456-493
[9]   THE ONTOGENY OF CANNABINOID RECEPTORS IN THE BRAIN OF POSTNATAL AND AGING RATS [J].
BELUE, RC ;
HOWLETT, AC ;
WESTLAKE, TM ;
HUTCHINGS, DE .
NEUROTOXICOLOGY AND TERATOLOGY, 1995, 17 (01) :25-30
[10]  
Berkovitz Ronny, 2011, Harefuah, V150, P884