Canseco-Alba Ana, Rodríguez-Manzo Gabriela
Departamento de Farmacobiología, CINVESTAV-Sede Sur, Calz. De los Tenorios 235, Col. Granjas Coapa, Ciudad de México 14330, Mexico.
Behav Brain Res. 2019 Feb 1;359:418-427. doi: 10.1016/j.bbr.2018.11.015. Epub 2018 Nov 12.
The endocannabinoid anandamide (AEA) transforms half of the population of previously non-copulating (NC) rats into sexually active animals in a long-lasting manner. The aim of this work was to explore the nature of this transformation. We identified the dose range in which AEA induces mating behavior in previously NC rats, which evidenced a dose-based, biphasic profile for AEA to induce the transformation of NC rats. We demonstrate that the sexual interaction with a receptive female, involving at least an intromission, is essential for AEA to induce the transformation of NC rats. This AEA-induced conversion is centrally mediated and involves the activation of CB1 receptors. Results indicate that the sexual impairment of this population of NC rats relies on their incapacity to initiate sexual activity and that an unidentified brain inhibitory influence on sexual behavior expression is removed by AEA treatment, allowing previously NC rats to show copulatory behavior in a long-lasting manner. The inhibitory influence is not removed by AEA treatment when animals are not allowed to have sexual contact with the female immediately after AEA injection. The same result was found for the opioid receptor antagonist naloxone, the other treatment reported to induce copulation in rats classified as NC. These data suggest that sexual behavior expression could depend on two different neural mechanisms at two different moments: one involved in the display of the first copulatory response and another responsible for maintaining subsequent sexual behavior responding.
内源性大麻素花生四烯乙醇胺(AEA)能使半数先前无交配行为(NC)的大鼠长期转变为性活跃动物。本研究旨在探究这种转变的本质。我们确定了AEA诱导先前NC大鼠出现交配行为的剂量范围,这证明了AEA诱导NC大鼠转变呈基于剂量的双相模式。我们证明,与处于接受状态的雌性进行性互动,至少包含一次插入动作,对于AEA诱导NC大鼠转变至关重要。这种由AEA诱导的转变是由中枢介导的,且涉及CB1受体的激活。结果表明,这群NC大鼠的性障碍在于它们无法启动性活动,而AEA处理可消除一种不明的对性行为表达的脑内抑制性影响,使先前的NC大鼠能够长期表现出交配行为。当动物在注射AEA后不立即与雌性进行性接触时,AEA处理无法消除这种抑制性影响。对于阿片受体拮抗剂纳洛酮也得到了相同的结果,纳洛酮是另一种据报道能诱导被归类为NC的大鼠进行交配的处理方法。这些数据表明,性行为表达可能在两个不同时刻依赖于两种不同的神经机制:一种参与首次交配反应的表现,另一种负责维持后续的性行为反应。