Department of Neurosciences and Behavior, Ribeirão Preto Medical School, University of São Paulo, Ribeirão Preto, Brazil.
National Institute of Science and Technology-Translational Medicine, Ribeirão Preto, São Paulo, Brazil.
Adv Exp Med Biol. 2021;1264:29-45. doi: 10.1007/978-3-030-57369-0_3.
Cannabis can synthetize more than 400 compounds, including terpenes, flavonoids, and more than 100 phytocannabinoids. The main phytocannabinoids are Δ-9-tetrahydrocannabinol (THC) and cannabidiol (CBD). Cannabis-based products are used as medicines in several countries. In this text, we present an overview of the main neurochemical mechanisms of action of the phytocannabinoids, especially THC and CBD. We also reviewed the indications and adverse effects of the main cannabis-based medicinal products. THC acts as a partial agonist at cannabinoid 1/2 receptors (CB). It is responsible for the characteristic effects of cannabis, such as euphoria, relaxation, and changes in perceptions. THC can also produce dysphoria, anxiety, and psychotic symptoms. THC is used therapeutically in nausea and vomiting due to chemotherapy, as an appetite stimulant, and in chronic pain. CBD acts as a noncompetitive negative allosteric modulator of the CB receptor, as an inverse agonist of the CB receptor, and as an inhibitor of the reuptake of the endocannabinoid anandamide. Moreover, CBD also activates 5-HT serotonergic receptors and vanilloid receptors. Its use in treatment-resistant epilepsy syndromes is approved in some countries. CBD does not produce the typical effects associated with THC and has anxiolytic and antipsychotic effects. Some of the most common adverse effects of CBD are diarrhea, somnolence, nausea, and transaminase elevations (with concomitant use of antiepileptics). The mechanisms of action involved in both the therapeutic and adverse effects of the phytocannabinoids are not fully understood, involving not only the endocannabinoid system. This "promiscuous" pharmacology could be responsible for their wide therapeutic spectrum.
大麻可以合成 400 多种化合物,包括萜烯、类黄酮和 100 多种植物大麻素。主要的植物大麻素是Δ-9-四氢大麻酚(THC)和大麻二酚(CBD)。大麻制品在一些国家被用作药物。在本文中,我们介绍了植物大麻素的主要神经化学作用机制概述,特别是 THC 和 CBD。我们还回顾了主要大麻类药物的适应证和不良反应。THC 作为大麻素 1/2 受体(CB)的部分激动剂。它是大麻的特征效应的原因,如欣快、放松和感知变化。THC 还可引起烦躁不安、焦虑和精神病症状。THC 被用于化疗引起的恶心和呕吐、食欲刺激和慢性疼痛的治疗。CBD 作为 CB 受体的非竞争性负变构调节剂、CB 受体的反向激动剂和内源性大麻素花生四烯酸的再摄取抑制剂。此外,CBD 还激活 5-HT 血清素受体和香草素受体。它在一些国家被批准用于治疗耐药性癫痫综合征。CBD 不会产生与 THC 相关的典型作用,具有抗焦虑和抗精神病作用。CBD 最常见的不良反应包括腹泻、嗜睡、恶心和转氨酶升高(与抗癫痫药合用)。植物大麻素的治疗和不良反应所涉及的作用机制尚未完全清楚,不仅涉及内源性大麻素系统。这种“混杂”的药理学可能是其广泛治疗谱的原因。