Trezza Viviana, Campolongo Patrizia, Cassano Tommaso, Macheda Teresa, Dipasquale Pasqua, Carratù Maria Rosaria, Gaetani Silvana, Cuomo Vincenzo
Department of Physiology and Pharmacology, Sapienza University of Rome, P. le A. Moro 5, 00185 Rome, Italy.
Psychopharmacology (Berl). 2008 Jul;198(4):529-37. doi: 10.1007/s00213-008-1162-3. Epub 2008 May 2.
The endocannabinoid system plays a crucial role in the control of emotionality and recent clinical findings have shown that heavy prenatal exposure to cannabis is significantly associated with self-reported anxiety symptoms in exposed children. However, the long-term neurobehavioral consequences of in utero exposure to low-moderate doses of cannabinoid compounds have never been investigated.
The objective of this study was to investigate whether perinatal exposure to moderate doses of the active constituent of cannabis, the CB(1) cannabinoid receptor agonist delta-9-tetrahydrocannabinol (THC), influences the emotional reactivity of rat offspring.
Primiparous Wistar rats were treated during pregnancy and lactation with doses of THC equivalent to the current estimates of moderate cannabis consumption in humans (2.5-5 mg kg(-1), per os, from gestational day 15 to postnatal day 9). The emotional reactivity of infant, adolescent, and adult offspring was investigated using the isolation-induced ultrasonic vocalization, social interaction, and elevated plus-maze tests, respectively.
Perinatal THC treatment did not affect parameters of reproduction; however, at the dose of 5 mg kg(-1), it increased the number of ultrasounds emitted by rat pups removed from the nest, inhibited social interaction and play behavior in the adolescent offspring, and induced an anxiogenic-like profile in the adult offspring tested in the elevated plus-maze test.
These results suggest that the endocannabinoid system is involved in the control of emotionality since early developmental stages. Thus, even moderate doses of cannabinoid compounds, when administered during the perinatal period, can have profound consequences for brain maturation, leading to long-lasting neurodevelopmental alterations.
内源性大麻素系统在情绪控制中起关键作用,近期临床研究结果表明,产前大量接触大麻与受影响儿童自我报告的焦虑症状显著相关。然而,子宫内接触低至中等剂量大麻素化合物的长期神经行为后果从未得到研究。
本研究的目的是调查围产期接触中等剂量大麻活性成分CB(1)大麻素受体激动剂δ-9-四氢大麻酚(THC)是否会影响大鼠后代的情绪反应。
初产Wistar大鼠在怀孕和哺乳期接受相当于目前估计人类中等大麻消费量的THC剂量治疗(从妊娠第15天至出生后第9天,经口给予2.5 - 5 mg kg(-1))。分别使用隔离诱导超声发声、社交互动和高架十字迷宫试验来研究幼年、青少年和成年后代的情绪反应。
围产期THC治疗不影响生殖参数;然而,在5 mg kg(-1)剂量下,它增加了从巢中取出的幼鼠发出的超声数量,抑制了青少年后代的社交互动和玩耍行为,并在高架十字迷宫试验中测试的成年后代中诱导出类似焦虑的表现。
这些结果表明,内源性大麻素系统从发育早期阶段就参与情绪控制。因此,即使在围产期给予中等剂量的大麻素化合物,也可能对大脑成熟产生深远影响,导致长期的神经发育改变。