Department of Pharmacology, School of Basic Medical Sciences, Xi'an Jiaotong University Health Science Center, Xi'an, 710061, China.
Neurosci Bull. 2019 Feb;35(1):156-166. doi: 10.1007/s12264-018-0286-7. Epub 2018 Sep 14.
Cardiovascular diseases are life-threatening illnesses with high morbidity and mortality. Suppressed vagal (parasympathetic) activity and increased sympathetic activity are involved in these diseases. Currently, pharmacological interventions primarily aim to inhibit over-excitation of sympathetic nerves, while vagal modulation has been largely neglected. Many studies have demonstrated that increased vagal activity reduces cardiovascular risk factors in both animal models and human patients. Therefore, the improvement of vagal activity may be an alternate approach for the treatment of cardiovascular diseases. However, drugs used for vagus nerve activation in cardiovascular diseases are limited in the clinic. In this review, we provide an overview of the potential drug targets for modulating vagal nerve activation, including muscarinic, and β-adrenergic receptors. In addition, vagomimetic drugs (such as choline, acetylcholine, and pyridostigmine) and the mechanism underlying their cardiovascular protective effects are also discussed.
心血管疾病是具有高发病率和死亡率的危及生命的疾病。抑制迷走神经(副交感神经)活动和增加交感神经活动与这些疾病有关。目前,药物干预主要旨在抑制交感神经的过度兴奋,而迷走神经调节在很大程度上被忽视。许多研究表明,增加迷走神经活动可以降低动物模型和人类患者的心血管危险因素。因此,提高迷走神经活动可能是治疗心血管疾病的另一种方法。然而,用于心血管疾病迷走神经激活的药物在临床上受到限制。在这篇综述中,我们提供了调节迷走神经激活的潜在药物靶点的概述,包括毒蕈碱和β-肾上腺素能受体。此外,还讨论了拟迷走神经药物(如胆碱、乙酰胆碱和吡啶斯的明)及其心血管保护作用的机制。