Oscar Langendorff Institute of Physiology, University of Rostock, Gertrudenstrasse 9, 18057, Rostock, Germany.
Department of Urology, University of Rostock, Rostock, Germany.
Pflugers Arch. 2024 Feb;476(2):243-256. doi: 10.1007/s00424-023-02877-x. Epub 2023 Nov 22.
Motility of detrusor smooth muscle includes adrenergic relaxation and cholinergic contraction. Since the latter may be deregulated in overactive bladder (OAB) pathophysiology, anticholinergics are the standard therapy but occasionally less tolerated due to side effects such as dry mouth and constipation. β adrenoceptor agonists also alleviate OAB symptoms by relaxing the detrusor muscle. Their age dependence, however, is far from understood. To address this issue, we induced contractions with KCl (60 mM) and carbachol (from 10 nM to 100 μM) in the presence of the β adrenoceptor agonist CL316,243 (from 0.1 to 10 μM) in both human and rat muscle strips. Our results confirmed that both contractions were attenuated by β adrenoceptor activation in both species, but with differing age dependence. In humans, specimens from mid-life subjects showed a significantly more pronounced effect of CL316,243 in attenuating carbachol-induced contractions than those from aged subjects (Cohen's d of maximal attenuation: 1.82 in mid-life versus 0.13 in aged) without altering EC. Conversely, attenuation of KCl responses by CL316,243 increased during ageing (Spearman correlation coefficient = -0.584, P<0.01). In rats, both KCl- and carbachol-induced contractions were significantly more attenuated by CL316,243 in samples from adolescent as compared to aged samples. Immunohistochemistry in human detrusor sections proved β adrenoreceptor abundance to remain unaltered during ageing. In conclusion, our findings suggest differential age-dependent changes in human β adrenoceptor-dependent attenuation of detrusor contraction in terms of electromechanical versus pharmacomechanical coupling; they may help understand the differential responsiveness of OAB patients to β agents.
逼尿肌平滑肌的运动包括肾上腺素能松弛和胆碱能收缩。由于后者在膀胱过度活动症 (OAB) 病理生理学中可能失调,因此抗胆碱能药物是标准治疗方法,但由于口干和便秘等副作用,偶尔耐受性较差。β肾上腺素受体激动剂也通过松弛逼尿肌来缓解 OAB 症状。然而,它们的年龄依赖性远未被理解。为了解决这个问题,我们在人类和大鼠肌肉条中,在存在β肾上腺素受体激动剂 CL316,243(从 0.1 到 10 μM)的情况下,用 KCl(60 mM)和卡巴胆碱(从 10 nM 到 100 μM)诱导收缩。我们的结果证实,两种收缩在两种物种中均被β肾上腺素受体激活减弱,但具有不同的年龄依赖性。在人类中,来自中年受试者的标本在减弱卡巴胆碱诱导的收缩方面显示出明显更明显的 CL316,243 作用,而来自老年受试者的标本则没有改变 EC(最大衰减的 Cohen's d:中年为 1.82,老年为 0.13)。相反,CL316,243 对 KCl 反应的衰减在衰老过程中增加(Spearman 相关系数 = -0.584,P<0.01)。在大鼠中,与老年样本相比,CL316,243 显著减弱了 KCl 和卡巴胆碱诱导的收缩。人类逼尿肌切片的免疫组织化学证明β肾上腺素受体丰度在衰老过程中保持不变。总之,我们的研究结果表明,在电机械与药理机械偶联方面,人类逼尿肌收缩的β肾上腺素受体依赖性衰减存在不同的年龄依赖性变化;它们可能有助于理解 OAB 患者对β 药物的不同反应性。