Castell D O
Am J Cardiol. 1985 Jan 25;55(3):210B-213B. doi: 10.1016/0002-9149(85)90633-2.
Calcium-channel blocking agents have a potential role in regulation of gastrointestinal tract function by decreasing smooth muscle contraction and possibly inhibiting cellular secretion. Most studies to date have concentrated on the ability of these drugs to inhibit smooth muscle contraction. Verapamil and diltiazem have been shown in animals (opossum, baboon) to produce decreased contractions in esophageal smooth muscle, resulting in a decreased amplitude of peristalsis and decreased lower esophageal sphincter pressures. In studies in man, oral doses of diltiazem and nifedipine have likewise been shown to have similar effects on the esophagus. At present, there is no experimental evidence of a major antisecretory effect of these drugs. In clinical trials, nifedipine has been shown to have a greater effect than placebo in improving symptoms in patients with achalasia, and diltiazem has been suggested as potential therapy in patients with chest pain secondary to excessive esophageal contraction. The precise role for calcium-channel blocking drugs in therapy of gastrointestinal disease is still being explored.
钙通道阻滞剂通过降低平滑肌收缩并可能抑制细胞分泌,在调节胃肠道功能方面具有潜在作用。迄今为止,大多数研究都集中在这些药物抑制平滑肌收缩的能力上。在动物(负鼠、狒狒)实验中已表明,维拉帕米和地尔硫䓬可使食管平滑肌收缩减弱,导致蠕动幅度减小和食管下括约肌压力降低。在人体研究中,口服地尔硫䓬和硝苯地平同样对食管有类似作用。目前,尚无实验证据表明这些药物有主要的抗分泌作用。在临床试验中,硝苯地平已被证明在改善贲门失弛缓症患者症状方面比安慰剂更有效,地尔硫䓬被建议作为食管过度收缩继发胸痛患者的潜在治疗药物。钙通道阻滞剂在胃肠道疾病治疗中的确切作用仍在探索中。