Wang Lei, Zhu Ting, Xu Hui-Bo, Pu Xiao-Ping, Zhao Xin, Tian Fang, Ding Tao, Sun Gui-Bo, Sun Xiao-Bo
Beijing Key Laboratory of Innovative Drug Discovery of Traditional Chinese Medicine (Natural Medicine) and Translational Medicine, Institute of Medicinal Plant Development, Peking Union Medical College and Chinese Academy of Medical Sciences, Key Laboratory of Bioactive Substances and Resources Utilization of Chinese Herbal Medicine, Ministry of Education, Institute of Medicinal Plant Development, Chinese Academy of Medical Sciences & Peking Union Medical College, Key Laboratory of New Drug Discovery based on Classic Chinese Medicine Prescription, Chinese Academy of Medical Sciences, Beijing, China.
Harbin University of Commerce, Harbin, China.
Ann Transl Med. 2021 Feb;9(3):246. doi: 10.21037/atm-20-4898.
Notoginseng leaf triterpenes (PNGL) is believed to have neuroprotective effects via the inhibition of inflammatory response and neuronal apoptosis. However, its mechanisms underlying the anti-ischemia/reperfusion (I/R) injury effects on the regulation of small molecule metabolism in rat brain remains unclear. The purpose of this study was thus to explore the mechanisms of PNGL on the regulation of small molecule metabolism in rat brain after I/R injury using matrix-assisted laser desorption ionization-mass spectrometry imaging (MALDI-MSI).
As a model of cerebral I/R injury, male Sprague-Dawley (SD) rats were established with a middle cerebral artery occlusion/reperfusion (MCAO/R) model after PNGL administration with 40 mg·kg through intraperitoneal injection (i.p.) for 7 days. We assessed the neurological behavior, regional cerebral blood flow (r CBF), neuron injury, and spatial distribution of metabolic small molecules.
Our results suggested that PNGL increased cerebral blood flow and relieved neurological dysfunction. Furthermore, using MALDI-MSI, we demonstrated that PNGL regulated 16 endogenous small molecules implicated in metabolic networks including tricarboxylic acid (TCA) cycle, adenosine triphosphate (ATP) metabolism, malate-aspartate shuttle, metal ions, and antioxidants underwent noticeable changes after reperfusion for 24 h.
PNGL is a novel cerebrovascular agent that can improve cerebral blood flow and attenuate adverse neurological disorders. The mechanisms are closely correlated with relative metabolic pathways, which offers insight into exploring new mechanisms in PNGL for the treatment of cerebral I/R injury.
三七叶总皂苷(PNGL)被认为可通过抑制炎症反应和神经元凋亡发挥神经保护作用。然而,其对大鼠脑缺血/再灌注(I/R)损伤后小分子代谢调控的潜在机制仍不清楚。因此,本研究旨在使用基质辅助激光解吸电离质谱成像(MALDI-MSI)探索PNGL对I/R损伤大鼠脑小分子代谢调控的机制。
以雄性Sprague-Dawley(SD)大鼠为脑I/R损伤模型,腹腔注射(i.p.)40mg·kg的PNGL,连续7天,建立大脑中动脉闭塞/再灌注(MCAO/R)模型。我们评估了神经行为、局部脑血流量(r CBF)、神经元损伤以及代谢小分子的空间分布。
我们的结果表明,PNGL增加了脑血流量并缓解了神经功能障碍。此外,使用MALDI-MSI,我们证明PNGL调节了16种参与代谢网络的内源性小分子,包括三羧酸(TCA)循环、三磷酸腺苷(ATP)代谢、苹果酸-天冬氨酸穿梭、金属离子,并且在再灌注24小时后抗氧化剂发生了显著变化。
PNGL是一种新型脑血管药物,可改善脑血流量并减轻不良神经障碍。其机制与相关代谢途径密切相关,这为探索PNGL治疗脑I/R损伤的新机制提供了思路。