Electrophysiology Lab, School of Biomedical Engineering, Indian Institute of Technology (BHU), Varanasi, India.
School of Biological and Biomedical Sciences, Galgotias University, Greater Noida, Uttar Pradesh, India.
Brain Inj. 2020 Apr 15;34(5):685-693. doi: 10.1080/02699052.2020.1726466. Epub 2020 Feb 17.
: Limited available therapeutics for ischemic stroke necessitate dire need of designing novel strategies for combating ischemic pathophysiological cascade among which neuroprotective strategies emerge as positive approaches. The neuropeptide prolactin is a pleiotropic hormone that affects various physiological conditions and reportedly combats neurotoxicity, neuronal stress and provides neuroprotection to hippocampal neurons .: The study explores the ability of prolactin in conferring neuroprotection in global cerebral ischemia and attempts to optimize the dose of prolactin which will be effective for the same.: Global cerebral ischemia was induced in male rats by bilateral common carotid occlusion (BCCAO) and different physiological and biochemical parameters were evaluated. Also, cerebral infarction and percentage of brain edema were measured.: The results revealed that prolactin significantly reduces cerebral infarct, brain water content and restores the physiological conditions like blood pressure, heart rate and cerebral blood flow. Also, prolactin markedly reduces the increased levels of the neurotransmitters (ɣ-aminobutyric acid and glutamate), cerebral calcium and nitrate in different brain compartments of ischemic rats.: Prolactin is able to ameliorate ischemia-reperfusion injury in rat brain and might be a potent candidate for further neuro-therapeutics development.
: 用于治疗缺血性中风的疗法有限,这迫切需要设计新的策略来对抗缺血性病理生理级联反应,其中神经保护策略是积极的方法。神经肽催乳素是一种多功能激素,它影响各种生理状况,据报道可对抗神经毒性、神经元应激,并为海马神经元提供神经保护。: 该研究探讨了催乳素在赋予全脑缺血性神经保护中的能力,并试图优化催乳素的剂量,使其对全脑缺血性具有治疗作用。: 通过双侧颈总动脉闭塞(BCCAO)诱导雄性大鼠全脑缺血,并评估了不同的生理和生化参数。还测量了脑梗死和脑水肿百分比。: 结果表明,催乳素可显著减少脑梗死、脑含水量,并恢复血压、心率和脑血流等生理状况。此外,催乳素还显著降低了缺血大鼠不同脑区神经递质(γ-氨基丁酸和谷氨酸)、脑钙和硝酸盐水平的升高。: 催乳素能够改善大鼠脑缺血再灌注损伤,可能是进一步神经治疗发展的有力候选药物。