Caution for Multidrug Therapy: Significant Baroreflex Afferent Neuroexcitation Coordinated by Multi-Channels/Pumps Under the Threshold Concentration of Yoda1 and Dobutamine Combination.

IF 4.8 2区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Biomolecules Pub Date : 2024-10-16 DOI:10.3390/biom14101311
Yin-Zhi Xu, Zhao-Yuan Xu, Hui-Xiao Fu, Mao Yue, Jia-Qun Li, Chang-Peng Cui, Di Wu, Bai-Yan Li
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引用次数: 0

Abstract

Multi-drug therapies are common in cardiovascular disease intervention; however, io channel/pump coordination has not been tested electrophysiologically. Apparently, inward currents were not elicited by Yoda1/10 nM or Dobutamine/100 nM alone in Ah-type baroreceptor neurons, but were by their combination. To verify this, electroneurography and the whole-cell patch-clamp technique were performed. The results showed that Ah- and C-volley were dramatically increased by the combination at 0.5 V and 5 V, in contrast to A-volley, as consistent with repetitive discharge elicited by step and ramp with markedly reduced current injection/stimulus intensity. Notably, a frequency-dependent action potential (AP) duration was increased with Iberiotoxin-sensitive K+ component. Furthermore, an increased peak in AP measured in phase plots suggested enhanced Na+ influx, cytoplasmic Ca2+ accumulation through reverse mode of Na+/Ca2+ exchanger, and, consequently, functional KCa1.1 up-regulation. Strikingly, the Yoda1- or Dbtm-mediated small/transient Na+/K+-pump currents were robustly increased by their combination, implying a quick ion equilibration that may also be synchronized by hyperpolarization-induced voltage-sag, enabling faster repetitive firing. These novel findings demonstrate multi-channel/pump collaboration together to integrate neurotransmission at the cellular level for baroreflex, providing an afferent explanation in sexual dimorphic blood pressure regulation, and raising the caution regarding the individual drug concentration in multi-drug therapies to optimize efficacy and minimize toxicity.

多种药物治疗需谨慎在 Yoda1 和多巴酚丁胺联合用药的阈值浓度下,多通道/泵协调产生了显著的气压反射传入神经兴奋。
多种药物疗法在心血管疾病干预中很常见;然而,io 通道/泵的协调性尚未经过电生理测试。很明显,在 Ah 型巴氏感受器神经元中,Yoda1/10 nM 或 Dobutamine/100 nM 不能单独激发内向电流,但它们的组合却能激发内向电流。为了验证这一点,我们采用了电神经图和全细胞膜片钳技术。结果表明,在 0.5 V 和 5 V 电压下,Ah- 和 C-波幅因组合而显著增加,与 A-波幅相反,这与阶跃和斜坡引起的重复放电一致,电流注入/刺激强度明显降低。值得注意的是,与频率相关的动作电位(AP)持续时间随着对伊比妥毒素敏感的 K+ 成分而增加。此外,在相位图中测量到的 AP 峰值增加表明 Na+ 流入增强,通过 Na+/Ca2+ 交换器的反向模式使细胞质 Ca2+ 积累,从而使 KCa1.1 功能上调。令人震惊的是,Yoda1 或 Dbtm 介导的小/瞬时 Na+/K+ 泵电流在它们的组合作用下强劲增加,这意味着离子的快速平衡也可能通过超极化诱导的电压下陷而同步化,从而实现更快的重复发射。这些新发现证明了多通道/泵共同协作在细胞水平整合神经传递以实现气压反射,为性双态血压调节提供了传入解释,并提高了对多种药物疗法中单个药物浓度的警惕,以优化疗效并减少毒性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Biomolecules
Biomolecules Biochemistry, Genetics and Molecular Biology-Molecular Biology
CiteScore
9.40
自引率
3.60%
发文量
1640
审稿时长
18.28 days
期刊介绍: Biomolecules (ISSN 2218-273X) is an international, peer-reviewed open access journal focusing on biogenic substances and their biological functions, structures, interactions with other molecules, and their microenvironment as well as biological systems. Biomolecules publishes reviews, regular research papers and short communications.  Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. There is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced.
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