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Involvement of NADPH-Dependent and cAMP-PKA Sensitive H~+ Channels in the Chorda Tympani Nerve Responses to Strong Acids

机译:NADPH依赖性和cAMP-PKA敏感的H〜+通道参与对强酸的Chorda Tympani神经反应

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To investigate if chorda tympani (CT) taste nerve responses to strong (HCl) and weak (CO2 and acetic acid) acidic stimuli are dependent upon NADPH oxidase-linked and cAMP-sensitive proton conductances in taste cell membranes, CT responses were monitored in rats, wild-type (WT) mice, and gp91~(phox) knockout (KO) mice in the absence and presence of blockers (Zn~(2+) and diethyl pyrocarbonate [DEPC]) or activators (8-(4-chlorophenylthio)-cAMP; 8-CPT-cAMP) of proton channels and activators of the NADPH oxidase enzyme (phorbol 12-myristate 13-acetate [PMA], H2O2, and nitrazepam). Zn~(2+) and DEPC inhibited and 8-CPT-cAMP, PMA, H2O2, and nitrazepam enhanced the tonic CT responses to HCl without altering responses to CO2 and acetic acid. In KO mice, the tonic HCl CT response was reduced by 64% relative to WT mice. The residual CT response was insensitive to H2O2 but was blocked by Zn~(2+). Its magnitude was further enhanced by 8-CPT-cAMP treatment, and the enhancement was blocked by 8-CPT-adenosine-3'-5'-cyclic monophospho-rothioate, a protein kinase A (PKA) inhibitor. Under voltage-clamp conditions, before cAMP treatment, rat tonic HCl CT responses demonstrated voltage-dependence only at ±90 mV, suggesting the presence of H~+ channels with voltage-dependent conductances. After cAMP treatment, the tonic HCl CT response had a quasi-linear dependence on voltage, suggesting that the cAMP-dependent part of the HCl CT response has a quasi-linear voltage dependence between +60 and -60 mV, only becoming sigmoidal when approaching +90 and -90 mV. The results suggest that CT responses to HCl involve 2 proton entry pathways, an NADPH oxidase-dependent proton channel, and a cAMP-PKA sensitive proton channel.
机译:为了研究鼓膜鼓膜(CT)对强(HCl)和弱(CO2和乙酸)酸性刺激的味觉神经反应是否依赖于味细胞膜中NADPH氧化酶联结和cAMP敏感的质子电导,对大鼠的CT反应进行了监测,野生型(WT)小鼠和gp91〜(phox)敲除(KO)小鼠,在没有和存在阻滞剂(Zn〜(2+)和焦碳酸二乙酯[DEPC])或活化剂(8-(4-氯苯硫基)的情况下-cAMP; 8-CPT-cAMP)质子通道和NADPH氧化酶的激活剂(佛波12-肉豆蔻酸酯13-醋酸酯[PMA],H2O2和硝西epa)。 Zn〜(2+)和DEPC受到抑制,而8-CPT-cAMP,PMA,H2O2和硝西epa增强了补强CT对HCl的响应,而没有改变对CO2和乙酸的响应。在KO小鼠中,相对于WT小鼠,补品HCl CT反应降低了64%。残留的CT反应对H2O2不敏感,但被Zn〜(2+)阻断。通过8-CPT-cAMP处理可进一步增强其强度,而通过蛋白激酶A(PKA)抑制剂8-CPT-腺苷-3'-5'-环一磷酸-硫代硫酸盐可阻止这种增强。在电压钳制条件下,在进行cAMP处理之前,大鼠补品HCl CT反应仅在±90 mV时表现出电压依赖性,这表明存在H〜+通道具有电压依赖性电导。经过cAMP处理后,补品HCl CT响应与电压呈准线性关系,这表明HCl CT响应的cAMP依赖部分与+60 -60 -60 mV之间呈拟线性电压相关性,仅在接近时变为S形。 +90和-90 mV。结果表明,CT对HCl的反应涉及2个质子进入途径,NADPH氧化酶依赖性质子通道和cAMP-PKA敏感质子通道。

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