Scott Department of Urology, Baylor College of Medicine, Houston, TX 77030, USA.
Brain Res Bull. 2013 Jun;95:40-5. doi: 10.1016/j.brainresbull.2013.03.006. Epub 2013 Apr 2.
We investigated the plasticity effects of diabetes mellitus and diuresis on the non-adrenergic non-cholinergic (NANC) and purinergic (P2X-type) contractile responses in longitudinal rat bladder strips. Female Sprague-Dawley rats received streptozotocin to induce diabetes, or sucrose in water to induce diuresis as a control condition for polyuria. Experiments were carried out at four weeks after treatments, using bladders from non-treated rats as control. Urinary bladder strips were electrically stimulated throughout the experiments to generate neurally evoked contractions (NEC). In all cases, P2X-mediated purinergic contractions were evaluated at the beginning and end of the stimulations with α,β-methylene-adenosine triphosphate (α,βMeATP). The NANC responses were assessed by using two independent protocols. First, cholinergic receptors were activated with carbachol (CCh), followed by inhibition of the muscarinic component with atropine. In the second protocol, the application order for CCh and atropine was reversed. The NANC response, unmasked with the application of atropine, and the P2X purinergic contractions were analyzed. NANC contractions in diabetic bladder strips are more resistant to the desensitizing effects caused by activation of cholinergic receptors. In early stages of experimental diabetes, NANC responses in diabetic strips are less sensitive to functional inhibition mediated by the cholinergic activation. However, P2X-mediated purinergic contractions are more sensitive to desensitization in diabetic or diuretic bladders. For instance preventing muscarinic receptor activation with atropine does not counteract the desensitization of purinergic contractions in either diabetic or diuretic strips. We suggest that diabetes may induce a plasticity of the NANC and P2X-mediated bladder contractile responses. The first one may be associated with diabetic neuropathic damage to bladder nerves, while impaired P2X purinergic contractions might be associated with detrusor hypertrophy observed in diabetic and diuretic strips.
我们研究了糖尿病和利尿作用对纵向大鼠膀胱条中非肾上腺素能非胆碱能(NANC)和嘌呤能(P2X 型)收缩反应的可塑性影响。雌性 Sprague-Dawley 大鼠接受链脲佐菌素诱导糖尿病,或蔗糖水诱导多尿作为多尿的对照条件。实验在治疗后四周进行,使用未处理大鼠的膀胱作为对照。在整个实验过程中,用电刺激膀胱产生神经诱发收缩(NEC)。在所有情况下,均在刺激开始和结束时使用α,β-亚甲基-三磷酸腺苷(α,βMeATP)评估 P2X 介导的嘌呤能收缩。通过两种独立的方案评估 NANC 反应。首先,用卡巴胆碱(CCh)激活胆碱能受体,然后用阿托品抑制毒蕈碱成分。在第二个方案中,反转了 CCh 和阿托品的应用顺序。应用阿托品揭示 NANC 反应,分析 P2X 嘌呤能收缩。糖尿病膀胱条中的 NANC 收缩对胆碱能受体激活引起的脱敏作用更具抗性。在实验性糖尿病的早期阶段,糖尿病条中的 NANC 反应对胆碱能激活介导的功能抑制的敏感性降低。然而,P2X 介导的嘌呤能收缩在糖尿病或利尿膀胱中更容易发生脱敏。例如,用阿托品防止毒蕈碱受体激活并不能对抗糖尿病或利尿条中嘌呤能收缩的脱敏作用。我们认为糖尿病可能引起 NANC 和 P2X 介导的膀胱收缩反应的可塑性。第一个可能与膀胱神经的糖尿病神经病变损伤有关,而受损的 P2X 嘌呤能收缩可能与糖尿病和利尿条中观察到的逼尿肌肥大有关。