Richelson E
Department of Research Pharmacology, Mayo Clinic Jacksonville, FL 32224.
Mayo Clin Proc. 1994 Nov;69(11):1069-81. doi: 10.1016/s0025-6196(12)61375-5.
To describe the clinical and basic pharmacologic properties of antidepressants and thus define the pharmacologic criteria for the ideal antidepressant.
A review of the pharmacologic characteristics of the newer second-generation antidepressants is presented in relationship to those of the older compounds.
Clinical pharmacologic and in vitro data on the synaptic effects of antidepressants (inhibition of synaptosomal uptake and blockade of neurotransmitter receptors) were obtained for the older antidepressants and for the more recently marketed and approved drugs. The group of antidepressants includes six new antidepressants approved for marketing since 1988 and two additional drugs marketed outside the United States as antidepressants but approved for use in the United States for obsessive-compulsive disorder. Thus, 18 antidepressant drugs are discussed.
All antidepressants seem to be equally efficacious in treating depression, and no drug seems to work more rapidly than another. Nonetheless, antidepressant drugs differ substantially in pharmacokinetic variables (elimination half-lives); in their effects on the metabolism of other drugs (by inhibiting the cytochrome P450 system); in their potencies for blocking the reuptake of norepinephrine, serotonin, and dopamine; and in their affinities for blocking histamine H1, muscarinic acetylcholine, alpha 1-adrenergic, and dopamine D2 receptors. Most side effects of antidepressants can be explained by their effects on blocking uptake and on blocking neurotransmitter receptors.
The newer second-generation antidepressants have distinct pharmacologic advantages in comparison with the tricyclic antidepressants and the older second-generation compounds. These advantages are clearly seen from their synaptic effects, in which most newer second-generation antidepressants are practically devoid of blocking effects at neurotransmitter receptors. Although the newer second-generation antidepressants are much closer to being the ideal antidepressant than are the older compounds, none completely fulfills the criteria for being the ideal drug.
描述抗抑郁药的临床和基本药理学特性,从而确定理想抗抑郁药的药理学标准。
综述新型第二代抗抑郁药与旧有化合物相关的药理学特征。
获取了关于旧有抗抑郁药以及最近上市并获批药物的临床药理学和抗抑郁药突触效应的体外数据(突触体摄取抑制和神经递质受体阻断)。抗抑郁药组包括自1988年以来获批上市的6种新型抗抑郁药以及另外两种在美国以外作为抗抑郁药上市但在美国获批用于强迫症治疗的药物。因此,共讨论了18种抗抑郁药。
所有抗抑郁药在治疗抑郁症方面似乎同样有效,且没有一种药物起效比另一种更快。尽管如此,抗抑郁药在药代动力学变量(消除半衰期)、对其他药物代谢的影响(通过抑制细胞色素P450系统)、阻断去甲肾上腺素、5-羟色胺和多巴胺再摄取的效力以及阻断组胺H1、毒蕈碱型乙酰胆碱、α1-肾上腺素能和多巴胺D2受体的亲和力方面存在显著差异。抗抑郁药的大多数副作用可通过其对摄取阻断和神经递质受体阻断的作用来解释。
与三环类抗抑郁药和旧有的第二代化合物相比,新型第二代抗抑郁药具有明显的药理学优势。从它们的突触效应中可以清楚地看到这些优势,其中大多数新型第二代抗抑郁药在神经递质受体处几乎没有阻断作用。尽管新型第二代抗抑郁药比旧有化合物更接近理想抗抑郁药,但没有一种能完全满足理想药物的标准。