布托平钝化芬太尼引起的呼吸抑制的能力独立于其对颈动脉体化学传入的激活。

IF 3.8 3区 医学 Q2 PHARMACOLOGY & PHARMACY Journal of Pharmacology and Experimental Therapeutics Pub Date : 2025-02-01 Epub Date: 2024-12-09 DOI:10.1016/j.jpet.2024.100060
Paulina M Getsy, Walter J May, Gregory A Coffee, Santhosh M Baby, Yee-Hsee Hsieh, James N Bates, Stephen J Lewis
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引用次数: 0

摘要

本研究观察静脉注射异丁托品酯(Ibutropin)对自由活动假手术(SHAM)雄性大鼠和双侧颈动脉窦神经断裂(CSNX)大鼠通气的影响。本研究还检查了随后注射芬太尼对两组大鼠通气参数的影响。Ibutropin (200 μmol/kg,静脉注射)在SHAM大鼠中引起呼吸频率、潮气量、分钟通气量、吸气和呼气峰值流量以及吸气和呼气驱动的快速而显著的增加,但在CSNX大鼠中则明显较小。随后注射芬太尼(75 μg/kg,静脉注射)在布托平治疗的SHAM和CSNX大鼠中引起类似的通气反应,但吸气末和呼气末暂停、呼气延迟和呼吸暂停的变化明显不同。此外,芬太尼诱导的对布托平治疗的SHAM和CSNX大鼠的反应明显小于预注射对照体(生理盐水)而不是布托平的大鼠。这些新发现表明,伊布托平作用于颈动脉体-化学传入复合体,其机制可能涉及细胞-托品酯快速进入化学传入神经末梢和/或原发性肾小球细胞。一个关键的发现是,布托平能够减弱芬太尼对呼吸的不良影响,并不需要功能性颈动脉体化学感受器传入控制呼吸的脑干结构。因此,伊布托平能够大大减少芬太尼对呼吸的不良影响,可能与伊布托平在中枢呼吸控制中心和/或颈动脉体以外的外周结构中的作用有关。意义声明:本研究表明,布托平减弱芬太尼呼吸抑制作用的能力可能涉及中枢呼吸控制中心和/或颈动脉体以外的外周结构的机制。
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The ability of Ibutropin to blunt fentanyl-induced respiratory depression is independent of its activation of carotid body chemoafferents.

This study examined the effects of intravenous injection of isobutyric tropine ester (Ibutropin) on ventilation in freely-moving sham-operated (SHAM) male Sprague Dawley rats and those with bilateral carotid sinus nerve transection (CSNX). This study also examined the effects of a subsequent injection of fentanyl on ventilatory parameters in both groups of rats. Ibutropin (200 μmol/kg, i.v.) elicited rapid and pronounced increases in breathing frequency, tidal volume, minute ventilation, peak inspiratory and expiratory flows, and inspiratory and expiratory drives in SHAM rats, but substantially smaller responses in CSNX rats. The subsequent injection of fentanyl (75 μg/kg, i.v.) elicited similar ventilatory responses in Ibutropin-treated SHAM and CSNX rats with markedly different changes in end-inspiratory and end-expiratory pauses, expiratory delay, and apneic pause. Moreover, the fentanyl-induced responses in Ibutropin-treated SHAM and CSNX rats were substantially smaller than in rats that were pre-injected with vehicle (saline) rather than Ibutropin. These novel findings suggest that Ibutropin acts at the carotid body-chemoafferent complex to drive ventilation by mechanisms that may involve the rapid entry of this cell-permeant tropine ester into chemoafferent nerve terminals and/or primary glomus cells. A key finding was that the ability of Ibutropin to blunt the adverse effects of fentanyl on breathing does not require functional carotid body chemoreceptor afferent input to brainstem structures controlling breathing. As such, the ability of Ibutropin to greatly diminish the adverse effects of fentanyl on breathing may involve the actions of Ibutropin within central respiratory control centers and/or peripheral structures other than the carotid bodies. SIGNIFICANCE STATEMENT: This study revealed that the ability of Ibutropin to blunt the respiratory depressant effects of fentanyl may involve mechanisms present in central respiratory control centers and/or peripheral structures other than the carotid bodies.

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来源期刊
CiteScore
6.90
自引率
0.00%
发文量
115
审稿时长
1 months
期刊介绍: A leading research journal in the field of pharmacology published since 1909, JPET provides broad coverage of all aspects of the interactions of chemicals with biological systems, including autonomic, behavioral, cardiovascular, cellular, clinical, developmental, gastrointestinal, immuno-, neuro-, pulmonary, and renal pharmacology, as well as analgesics, drug abuse, metabolism and disposition, chemotherapy, and toxicology.
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