Poller U, Nedelka G, Radke J, Pönicke K, Brodde O E
Institut für Pharmakologie und Toxikologie, Universität Halle-Wittenberg, Germany.
J Am Coll Cardiol. 1997 Jan;29(1):187-93. doi: 10.1016/s0735-1097(96)00437-8.
This study was conducted to determine possible age-dependent changes in the responsiveness of human cardiac muscarinic receptors.
It is well known that the baroreflex activity decreases with aging. However, the mechanisms underlying this phenomenon are not completely understood at present.
In six healthy young (mean [+/-SEM] age 26 +/- 2 years) and six healthy older volunteers (mean age 60 +/- 2 years), we determined 1) the effects of graded doses of atropine (bolus application, six doses, each for 20 min, range 0.03 to 0.96 mg) and the M1-cholinoceptor selective antagonist pirenzepine (bolus application, eight doses, each for 20 min, range 0.04 to 10 mg) on heart rate, blood pressure and systolic time intervals (as measure of inotropism); and 2) the baroreflex activity by assessing the bradycardic response to phenylephrine.
Atropine and pirenzepine caused biphasic effects on heart rate: At lower doses (< 0.12 mg for atropine, < 5 mg for pirenzepine) they decreased heart rate, whereas at higher doses they increased heart rate. Heart rate decreases induced by both antimuscarinic drugs were significantly larger in the young volunteers than in the older volunteers, whereas heart rate increases were not significantly different for both drugs. Atropine and pirenzepine did not significantly affect blood pressure and systolic time intervals. Infusion of graded doses of phenylephrine (four doses ranging from 0.1 to 1.0 microgram/kg body weight per min for 15 min each) caused a higher increase in systolic blood pressure and a smaller decrease in heart rate at each dose in the older volunteers than in the young volunteers. The slopes of the regression lines were 16 +/- 2.3 ms/mm Hg for the young and 6 +/- 0.5 ms/mm Hg for the older volunteers (p < 0.01).
Human cardiac muscarinic receptor activity is diminished with increasing age; such decreased cardiac muscarinic receptor activity could contribute to the decrease in baroreflex activity with aging. In contrast, antimuscarinic drugs seem to have no effect on human cardiac contractility.
本研究旨在确定人类心脏毒蕈碱受体反应性可能存在的年龄依赖性变化。
众所周知,压力反射活动会随着年龄增长而降低。然而,目前对这一现象背后的机制尚未完全理解。
在6名健康年轻志愿者(平均年龄[±标准误]26±2岁)和6名健康老年志愿者(平均年龄60±2岁)中,我们测定了:1)不同剂量阿托品(静脉推注,6个剂量,每个剂量持续20分钟,范围为0.03至0.96毫克)和M1胆碱能受体选择性拮抗剂哌仑西平(静脉推注,8个剂量,每个剂量持续20分钟,范围为0.04至10毫克)对心率、血压和收缩期时间间期(作为心肌收缩力的指标)的影响;2)通过评估对去氧肾上腺素的心动过缓反应来测定压力反射活动。
阿托品和哌仑西平对心率产生双相作用:在较低剂量时(阿托品<0.12毫克,哌仑西平<5毫克),它们会降低心率,而在较高剂量时则会增加心率。两种抗毒蕈碱药物引起的心率降低在年轻志愿者中比在老年志愿者中显著更大,而两种药物引起的心率增加没有显著差异。阿托品和哌仑西平对血压和收缩期时间间期没有显著影响。静脉输注不同剂量的去氧肾上腺素(4个剂量,范围为每分钟0.1至1.0微克/千克体重,每个剂量持续15分钟),在每个剂量下,老年志愿者的收缩压升高幅度更高,心率降低幅度更小,与年轻志愿者相比。年轻志愿者的回归线斜率为16±2.3毫秒/毫米汞柱,老年志愿者为6±0.5毫秒/毫米汞柱(p<0.01)。
随着年龄增长,人类心脏毒蕈碱受体活性降低;这种心脏毒蕈碱受体活性的降低可能导致压力反射活动随年龄增长而降低。相比之下,抗毒蕈碱药物似乎对人类心脏收缩力没有影响。