首页> 外文期刊>American Journal of Physiology >Thermal sensitivity of isolated vagal pulmonary sensory neurons: role of transient receptor potential vanilloid receptors.
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Thermal sensitivity of isolated vagal pulmonary sensory neurons: role of transient receptor potential vanilloid receptors.

机译:离体迷走性肺部感觉神经元的热敏感性:瞬态受体电位香草素受体的作用。

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A recent study has demonstrated that increasing the intrathoracic temperature from 36 degrees C to 41 degrees C induced a distinct stimulatory and sensitizing effect on vagal pulmonary C-fiber afferents in anesthetized rats (J Physiol 565: 295-308, 2005). We postulated that these responses are mediated through a direct activation of the temperature-sensitive transient receptor potential vanilloid (TRPV) receptors by hyperthermia. To test this hypothesis, we studied the effect of increasing temperature on pulmonary sensory neurons that were isolated from adult rat nodose/jugular ganglion and identified by retrograde labeling, using the whole cell perforated patch-clamping technique. Our results showed that increasing temperature from 23 degrees C (or 35 degrees C) to 41 degrees C in a ramp pattern evoked an inward current, which began to emerge after exceeding a threshold of approximately 34.4 degrees C and then increased sharply in amplitude as the temperature was further increased, reaching a peak current of 173 +/- 27 pA (n = 75) at 41 degrees C. The temperature coefficient, Q10, was 29.5 +/- 6.4 over the range of 35-41 degrees C. The peak inward current was only partially blocked by pretreatment with capsazepine (Delta I = 48.1 +/- 4.7%, n = 11) or AMG 9810 (Delta I = 59.2 +/- 7.8%, n = 8), selective antagonists of the TRPV1 channel, but almost completely abolished (Delta I = 96.3 +/- 2.3%) by ruthenium red, an effective blocker of TRPV1-4 channels. Furthermore, positive expressions of TRPV1-4 transcripts and proteins in these neurons were demonstrated by RT-PCR and immunohistochemistry experiments, respectively. On the basis of these results, we conclude that increasing temperature within the normal physiological range can exert a direct stimulatory effect on pulmonary sensory neurons, and this effect is mediated through the activation of TRPV1, as well as other subtypes of TRPV channels.
机译:最近的一项研究表明,将胸腔内温度从36摄氏度提高到41摄氏度,会对麻醉大鼠的迷走性肺C纤维传入神经产生明显的刺激和致敏作用(生理学杂志565:295-308,2005)。我们假设这些反应是通过热疗直接激活温度敏感的瞬态受体电位香草(TRPV)受体介导的。为了验证这一假设,我们研究了温度升高对从成年大鼠结节/颈神经节分离并通过逆向标记使用全细胞穿孔膜片钳技术鉴定的肺部感觉神经元的影响。我们的结果表明,以斜坡模式将温度从23摄氏度(或35摄氏度)升高到41摄氏度会引起内向电流,该电流在超过约34.4摄氏度的阈值后开始出现,然后随着温度的升高幅度急剧增加。温度进一步升高,在41摄氏度达到峰值电流173 +/- 27 pA(n = 75)。温度系数Q10在35-41摄氏度范围内为29.5 +/- 6.4。用卡普西平(Delta I = 48.1 +/- 4.7%,n = 11)或AMG 9810(Delta I = 59.2 +/- 7.8%,n = 8),TRPV1通道的选择性拮抗剂预处理只能部分阻止内向电流,但被TRPV1-4通道的有效阻断剂钌红几乎完全废除了(ΔI = 96.3 +/- 2.3%)。此外,分别通过RT-PCR和免疫组织化学实验证明了在这些神经元中TRPV1-4转录物和蛋白的阳性表达。根据这些结果,我们得出结论,在正常生理范围内升高温度可以对肺部感觉神经元产生直接刺激作用,并且这种作用是通过激活TRPV1以及TRPV通道的其他亚型介导的。

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