Department of Molecular Pharmacology and Physiology, Morsani College of Medicine, University of South Florida, Tampa, Florida.
J Appl Physiol (1985). 2023 Feb 1;134(2):307-315. doi: 10.1152/japplphysiol.00495.2022. Epub 2023 Jan 5.
Inhalation of noxious irritants activates nociceptive sensory afferent nerves innervating the airways, inducing reflex regulation of autonomic networks and the modulation of respiratory drive and cardiovascular (CV) parameters such as heart rate and blood pressure. In healthy mammals, irritant-evoked pulmonary-cardiac reflexes cause parasympathetic-mediated bradycardia. However, in spontaneously hypertensive (SH) rats, irritant inhalation also increases sympathetic drive to the heart. This remodeled pulmonary-cardiac reflex may contribute to cardiovascular risk caused by inhalation of air pollutants/irritants in susceptible individuals with cardiovascular disease (CVD). Previous studies have shown that the cooling mimic l-menthol, an agonist for the cold-sensitive transient receptor potential melastatin 8 (TRPM8), can alleviate nasal inflammatory symptoms and respiratory reflexes evoked by irritants. Here, we investigated the impact of inhalation of TRPM8 agonists l-menthol and WS-12 on pulmonary-cardiac reflexes evoked by inhalation of the irritant allyl isothiocyanate (AITC) using radiotelemetry. l-Menthol, but not its inactive analog d-menthol, significantly reduced the AITC-evoked reflex tachycardia and premature ventricular contractions (PVCs) in SH rats but had no effect on the AITC-evoked bradycardia in either SH or normotensive Wistar-Kyoto (WKY) rats. WS-12 reduced AITC-evoked tachycardia and PVCs in SH rats, but this more potent TRPM8 agonist also reduced AITC-evoked bradycardia. l-Menthol had no effect on heart rate when given alone, whereas WS-12 evoked a minor bradycardia in WKY rats. We conclude that stimulation of TRPM8-expressing afferents within the airways reduces irritant-evoked pulmonary-cardiac reflexes, especially the aberrant reflex tachyarrhythmia in SH rats. Airway menthol treatment may be an effective therapy for reducing pollution-associated CV exacerbations. Irritant-evoked pulmonary-cardiac reflexes are remodeled in spontaneously hypertensive (SH) rats-causing de novo sympathetic reflexes that drive tachyarrhythmia. This remodeling may contribute to air pollution-associated risk in susceptible individuals with cardiovascular disease. We found that inhalation of TRPM8 agonists, l-menthol and WS-12, but not the inactive analog d-menthol, selectively reduces the reflex tachyarrhythmia evoked by allyl isothiocyanate (AITC) inhalation in SH rats. Use of menthol may protect susceptible individuals from pollution-associated CV exacerbations.
吸入有害刺激物会激活支配气道的伤害性感觉传入神经,诱发自主神经网络的反射调节和呼吸驱动以及心血管(CV)参数的调制,如心率和血压。在健康的哺乳动物中,刺激物诱发的肺-心反射引起迷走神经介导的心动过缓。然而,在自发性高血压(SH)大鼠中,刺激物吸入也会增加心脏的交感神经驱动。这种重塑的肺-心反射可能导致易患心血管疾病(CVD)的个体吸入空气污染物/刺激物引起心血管风险。先前的研究表明,冷敏瞬时受体电位 melastatin 8(TRPM8)的激动剂冷却模拟薄荷醇 l-可以缓解由刺激物引起的鼻炎症症状和呼吸反射。在这里,我们使用无线电遥测技术研究了吸入 TRPM8 激动剂薄荷醇 l-和 WS-12 对丙烯基异硫氰酸酯(AITC)吸入引起的肺-心反射的影响。薄荷醇 l-,而不是其无活性类似物薄荷脑 d-,可显著减轻 SH 大鼠 AITC 诱发的反射性心动过速和室性早搏(PVCs),但对 SH 或正常血压 Wistar-Kyoto(WKY)大鼠的 AITC 诱发的心动过缓无影响。WS-12 可降低 SH 大鼠 AITC 诱发的心动过速和 PVCs,但这种更强效的 TRPM8 激动剂也降低了 AITC 诱发的心动过缓。薄荷醇 l-单独使用时对心率没有影响,而 WS-12 则使 WKY 大鼠出现轻微的心动过缓。我们得出结论,气道内表达 TRPM8 的传入纤维的刺激可减轻刺激物诱发的肺-心反射,特别是 SH 大鼠异常的反射性心动过速。气道薄荷醇治疗可能是一种有效的治疗方法,可减少与污染相关的心血管恶化。自发性高血压(SH)大鼠的刺激物诱发的肺-心反射被重塑-引起新的交感神经反射,驱动心动过速。这种重塑可能导致易患心血管疾病的个体与空气污染相关的风险增加。我们发现,吸入 TRPM8 激动剂薄荷醇 l-和 WS-12,但不是无活性类似物薄荷脑 d-,可选择性地降低 SH 大鼠吸入丙烯基异硫氰酸酯(AITC)引起的反射性心动过速。使用薄荷醇可能会保护易受影响的个体免受与污染相关的心血管恶化。