Stimulatory effect of methylglyoxal on capsaicin-sensitive lung vagal afferents in rats: role of TRPA1.

IF 2.2 3区 医学 Q3 PHYSIOLOGY
You Shuei Lin, Nai-Ju Chan, Pei-Yu Xiao, Ching Jung Lai
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引用次数: 0

Abstract

Methylglyoxal (MG), a reactive metabolic byproduct of glycolysis, is a causative of painful diabetic neuropathy. Patients with diabetes are associated with more frequent severe asthma exacerbation. Stimulation of capsaicin-sensitive lung vagal (CSLV) afferents may contribute to the pathogenesis of hyperreactive airway diseases such as asthma. However, the possibility of the stimulatory effect of MG on CSLV afferents and the underlying mechanisms remain unknown. Our results showed that intravenous injection of MG (25 mg/kg, MG25) in anesthetized, spontaneously breathing rats elicited pulmonary chemoreflexes characterized by apnea, bradycardia, and hypotension. The MG-induced apneic response was reproducible and dose dependent. MG25 no longer evoked these reflex responses after perineural capsaicin treatment of both cervical vagi to block C-fibers' conduction, suggesting that the reflexes were mediated through the stimulation of CSLV afferents. Pretreatment with HC030031 [an antagonist of transient receptor potential ankyrin subtype 1 protein (TRPA1)] or AP18 (another TRPA1 antagonist), but not their vehicle, markedly attenuated the apneic response induced by MG25. Consistently, electrophysiological results showed that pretreatment with HC030031 largely attenuated the intense discharge in CSLV afferents induced by injection of MG25 in open-chest and artificially ventilated rats. In isolated CSLV neurons, the perfusion of MG evoked an abrupt and pronounced increase in calcium transients in a concentration-dependent manner. This stimulatory effect on CSLV neurons was also abolished by HC030031 treatment but not by its vehicle. In conclusion, these results suggest that MG exerts a stimulatory effect on CSLV afferents, inducing pulmonary chemoreflexes, and such stimulation is mediated through the TRPA1 activation.NEW & NOTEWORTHY Methylglyoxal (MG) is implicated in the development of painful diabetic neuropathy. A retrospective cohort study revealed an increased incidence of asthma exacerbations in patients with diabetes. This study demonstrated that elevated circulating MG levels stimulate capsaicin-sensitive lung vagal afferents via activation of TRPA1, which in turn triggers respiratory reflexes. These findings provide new information for understanding the pathogenic mechanism of diabetes-associated hyperreactive airway diseases and potential therapy.

甲基乙二醛对大鼠对辣椒素敏感的肺迷走神经传入的刺激作用:TRPA1 的作用。
甲基乙二醛(MG)是糖酵解过程中产生的一种反应性代谢副产物,是导致糖尿病神经病变疼痛的原因之一。糖尿病患者会更频繁地出现严重的哮喘恶化。刺激对辣椒素敏感的肺迷走神经(CSLV)传入可能是哮喘等高反应性气道疾病的发病机制之一。然而,MG对CSLV传入的刺激作用的可能性及其潜在机制仍然未知。我们的研究结果表明,给麻醉的自主呼吸大鼠静脉注射 MG(25 毫克/千克,MG25)可引起肺化学反射,其特征是呼吸暂停、心动过缓以及低血压。MG 诱导的呼吸暂停反应具有再现性和剂量依赖性。在对两个颈迷走神经进行硬膜外辣椒素处理以阻断 C 纤维传导后,MG25 不再诱发这些反射反应,这表明反射是通过刺激 CSLV 传入神经介导的。使用 HC030031(瞬时受体电位杏仁蛋白亚型 1 蛋白(TRPA1)拮抗剂)或 AP18(另一种 TRPA1 拮抗剂)进行预处理,而不使用它们的载体,可明显减轻 MG25 引起的呼吸暂停反应。同样,电生理学结果表明,在开胸大鼠和人工通气大鼠体内注射 MG25 后,HC030031 在很大程度上抑制了 CSLV 传入神经的强烈放电。在离体的 CSLV 神经元中,MG 的灌注以浓度依赖的方式诱发了钙离子瞬态的突然和显著增加。HC030031 也能消除对 CSLV 神经元的这种刺激作用,但其载体却不能。总之,这些结果表明 MG 对 CSLV 传入神经有刺激作用,可诱导肺化学反射,这种刺激是通过 TRPA1 激活介导的。
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来源期刊
CiteScore
5.30
自引率
3.60%
发文量
145
审稿时长
2 months
期刊介绍: The American Journal of Physiology-Regulatory, Integrative and Comparative Physiology publishes original investigations that illuminate normal or abnormal regulation and integration of physiological mechanisms at all levels of biological organization, ranging from molecules to humans, including clinical investigations. Major areas of emphasis include regulation in genetically modified animals; model organisms; development and tissue plasticity; neurohumoral control of circulation and hypertension; local control of circulation; cardiac and renal integration; thirst and volume, electrolyte homeostasis; glucose homeostasis and energy balance; appetite and obesity; inflammation and cytokines; integrative physiology of pregnancy-parturition-lactation; and thermoregulation and adaptations to exercise and environmental stress.
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