Fride E, Mechoulam R
Department of Natural Products, Hebrew University of Jerusalem, Faculty of Medicine, Israel.
Psychoneuroendocrinology. 1996 Feb;21(2):157-72. doi: 10.1016/0306-4530(95)00039-9.
Recent breakthroughs in cannabinoid research, including the identification of two cannabinoid receptors (CB receptors) and a family of endogenous ligands, the anandamides, may shed new light on the sequelae of pre- and perinatal exposure to cannabinoid receptor ligands and enable the experimental manipulation of the endogenous ligand in the developing organism. In the present study we examined the behavioural response to anandamide (ANA) in developing mice from day 13 into adulthood. We observed that depression of ambulation in an open field and the analgetic response to ANA are not fully developed until adulthood. In a separate set of experiments, we administered five daily injections of ANA (SC, 20 mg/kg) during the last trimester of pregnancy. No effects on birth weight, litter size, sex ratio and eye opening were detected after maternal ANA treatment. Further, no effects on open field performance of the offspring were observed until 4 weeks of age. However, from 40 days of age, a number of differences between the prenatal ANA and control offspring were detected. Thus, the offspring from ANA-treated dams showed impaired responsiveness to a challenge with ANA or delta 0-THC expressed as a lack of immobility in the ring test for catalepsy, hypothermia and analgesia. On the other hand, without challenge, they exhibited a spontaneous decrease in open field activity, catalepsy, hypothermia and a hypoalgetic tendency. These data suggest that exposure to excessive amounts of ANA during gestation alters the functioning of the ANA-CB receptor system. Further experiments investigating responsivity of the immune system suggest an increased inflammatory response to arachidonic acid, and enhanced hypothermic response to lipopolysaccharide in prenatally treated offspring. The results are discussed in relation to other manipulations of the maternal milieu, especially prenatal stress. It is concluded that alterations induced by prenatal exposure to ANA, cannabinoids and other psychotropic drugs or prenatal stress, share common features, but the data also suggest specific effects on the ANA-CB receptor system.
大麻素研究领域的最新突破,包括两种大麻素受体(CB受体)和一类内源性配体——花生四烯乙醇胺的鉴定,可能会为产前和围产期接触大麻素受体配体的后遗症带来新的启示,并能够在发育中的生物体中对这种内源性配体进行实验性操控。在本研究中,我们检测了从出生第13天到成年期的发育中小鼠对花生四烯乙醇胺(ANA)的行为反应。我们观察到,在旷场中自主活动的减少以及对ANA的镇痛反应直到成年期才完全发育。在另一组实验中,我们在妊娠最后三个月每天皮下注射五次ANA(20mg/kg)。母体给予ANA处理后,未检测到对出生体重、窝仔数、性别比例和睁眼的影响。此外,在后代4周龄之前,未观察到对其旷场行为表现的影响。然而,从40日龄起,检测到产前给予ANA的后代与对照后代之间存在一些差异。因此,经ANA处理的母鼠所产后代在接受ANA或δ⁹-四氢大麻酚(delta ⁹-THC)激发时反应受损,表现为在僵住症、体温过低和镇痛的环形试验中缺乏不动反应。另一方面,在没有激发的情况下,它们在旷场活动、僵住症、体温过低和镇痛倾向方面出现自发下降。这些数据表明,孕期接触过量的ANA会改变ANA-CB受体系统的功能。进一步研究免疫系统反应性的实验表明,产前处理的后代对花生四烯酸的炎症反应增强,对脂多糖的体温过低反应增强。结合对母体环境的其他操控,尤其是产前应激,对这些结果进行了讨论。得出的结论是,产前接触ANA、大麻素和其他精神药物或产前应激所引起的改变具有共同特征,但数据也表明对ANA-CB受体系统有特定影响。