神经肽 Y2 受体激动剂 NPY13-36 对自发性高血压大鼠短暂局灶性脑缺血的神经和血管保护潜力

IF 2.9 3区 医学 Q2 NEUROSCIENCES Neuroscience Pub Date : 2024-10-19 DOI:10.1016/j.neuroscience.2024.10.035
Łukasz Przykaza , Helena Domin , Maria Śmiałowska , Luiza Stanaszek , Paweł M. Boguszewski , Ewa Kozniewska
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摘要

大量体外和体内实验研究表明,神经肽 Y2 受体(Y2R)是神经保护疗法的潜在靶点,包括对健康大鼠缺血性脑卒中的神经保护。由于人类脑卒中通常与合并症有关,而长期高血压是导致脑卒中的最常见合并症,因此本研究旨在评估 Y2R 激动剂 NPY13-36 对接受 90 分钟大脑中动脉缝合闭塞和随后再灌注(MCAOR)的本质性高血压(SHR)大鼠的神经保护潜力。用激光多普勒血流仪连续监测缺血灶和半影区的大脑皮层微血流。在缺血或再灌注早期,脑室内注射 NPY13-36(10 μg/6 μl 生理盐水)。研究了梗死面积(三苯基氯化四氮唑染色)、行为测试(步态、活动能力和感觉运动功能)以及半影区大脑皮层微循环对高碳酸血症和一氧化氮合成抑制的反应。我们的研究结果表明,在再灌注期间给予 NPY13-36 可缩小梗死面积、改善运动功能并恢复微循环对一氧化氮合酶阻断的反应。这项研究的新颖之处在于发现了 NPY13-36 在脑缺血/再灌注中的血管保护作用。此外,这项研究还证明了 NPY13-36 对本质性高血压动物的有益作用,并表明 Y2R 配体可能是治疗这种疾病的脑缺血候选药物。
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Neuro- and vasoprotective potential of neuropeptide Y2 receptor agonist, NPY13-36, against transient focal cerebral ischemia in spontaneously hypertensive rats
Numerous in vitro and in vivo experimental studies indicate that neuropeptide Y Y2 receptors (Y2R) are potential targets for neuroprotective therapy, including neuroprotection against ischemic stroke in healthy rats. Since stroke in humans is typically associated with comorbidities and long-term hypertension is the most common comorbidity leading to stroke, this study aimed to assess the neuroprotective potential of the Y2R agonist NPY13–36 in the rats with essential hypertension (SHR) subjected to 90 min middle cerebral artery suture occlusion with subsequent reperfusion (MCAOR). The cerebrocortical microflow in the ischemic focus and penumbra was continuously monitored with a Laser-Doppler flowmeter. NPY13–36 (10 μg/6 μl physiological saline solution) was administered intracerebroventricularly (i.c.v.) during ischemia or early reperfusion. The infarct area (triphenyltetrazolium chloride staining), behavioral tests (gait, mobility, and sensorimotor functions), and the response of the cerebrocortical microcirculation in the penumbra to hypercapnia and to the inhibition of the synthesis of nitric oxide were studied. Our results demonstrate that administration of NPY13-36 reduces the size of the infarct, improves motor functions, and restores microcirculatory response to the blockade of nitric oxide synthase when administered during reperfusion. The novelty of this study is a finding of the vasoprotective effect of NPY13-36 in brain ischemia/reperfusion. Moreover, this study provides evidence of the beneficial effects of NPY13-36 in animals with essential hypertension and indicates that Y2R ligands may be promising candidates for treating the ischemic brain in the case of this disease.
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来源期刊
Neuroscience
Neuroscience 医学-神经科学
CiteScore
6.20
自引率
0.00%
发文量
394
审稿时长
52 days
期刊介绍: Neuroscience publishes papers describing the results of original research on any aspect of the scientific study of the nervous system. Any paper, however short, will be considered for publication provided that it reports significant, new and carefully confirmed findings with full experimental details.
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