Qizhi Kebitong Formula Ameliorates Sciatic Nerve Injury in Streptozocin-induced Diabetic Mice through PERK/ATF4/CHOP Endoplasmic Reticulum Stress Signaling Pathway.

IF 2.6 4区 医学 Q2 PHARMACOLOGY & PHARMACY
Honghai Yu, Cunqing Yang, Guoqiang Wang, Jiao Lv, Xiangyan Li, Wenxiu Qi, Xiuge Wang
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Abstract

Background: The Qizhi Kebitong formula (QKF) has been utilized as a traditional Chinese medicine (TCM) remedy for over two decades in treating diabetic peripheral neuropathy (DPN) with notable clinical efficacy. However, its precise mechanism and bioactive constituents remain elusive.

Methods: Through Ultra-high performance liquid chromatography-quadrupole time-of-flight mass spectrometry (UHPLC/QTOF-MS) analysis was used to identify the primary components of QKF. Nerve conduction function in mice was assessed by measuring sensory thresholds and nerve conduction velocities. Laser speckle contrast imaging (LSCI) was used to examine the effect of QKF on foot pads and perineural blood flow in mice. Additionally, Transmission electron microscopy (TEM) and various pathologic stains were utilized to observe QKF's therapeutic effect on sciatic nerve (SN) damage in DPN mice. The impact of QKF on the pathological mechanism of the DPN model was explored through qRT-PCR, western blot, and immunohistochemistry.

Results: Our results demonstrated that QKF improved phenotypic features in a mouse model of DPN, increased blood flow around the foot pad and SN, and somewhat repaired the pathological structure and function of SN. Furthermore, the study revealed that QKF slowed down the progression of DPN by inhibiting the endoplasmic reticulum (ER) stress apoptosis signaling pathway mediated by PERK/ATF4/CHOP pathway.

Conclusion: The significant neuroprotective effects of QKF in experimental DPN mice were confirmed by our findings, which offer important scientific evidence supporting its potential utilization in DPN treatment.

芪脂克痹通方通过PERK/ATF4/CHOP内质网应激信号通路改善链脲佐菌素诱导的糖尿病小鼠坐骨神经损伤
背景:芪脂克痹通方治疗糖尿病周围神经病变(DPN)已有二十多年的历史,临床疗效显著。然而,其确切的机制和生物活性成分尚不清楚。方法:采用超高效液相色谱-四极杆飞行时间质谱(UHPLC/QTOF-MS)分析方法,对芪芩f的主要成分进行鉴定。通过测量感觉阈值和神经传导速度来评估小鼠的神经传导功能。采用激光散斑对比成像(LSCI)方法观察芪芩汤对小鼠足垫及神经周血流的影响。通过透射电镜(TEM)和各种病理染色观察芪芩方对DPN小鼠坐骨神经损伤的治疗作用。通过qRT-PCR、western blot、免疫组化等方法探讨QKF对DPN模型病理机制的影响。结果:我们的研究结果表明,QKF改善了DPN小鼠模型的表型特征,增加了足垫和SN周围的血流量,并在一定程度上修复了SN的病理结构和功能。此外,研究发现,QKF通过抑制PERK/ATF4/CHOP通路介导的内质网(ER)应激凋亡信号通路,减缓DPN的进展。结论:清肾方对实验性DPN小鼠具有明显的神经保护作用,为其在DPN治疗中的应用提供了重要的科学依据。
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来源期刊
CiteScore
6.30
自引率
0.00%
发文量
302
审稿时长
2 months
期刊介绍: Current Pharmaceutical Design publishes timely in-depth reviews and research articles from leading pharmaceutical researchers in the field, covering all aspects of current research in rational drug design. Each issue is devoted to a single major therapeutic area guest edited by an acknowledged authority in the field. Each thematic issue of Current Pharmaceutical Design covers all subject areas of major importance to modern drug design including: medicinal chemistry, pharmacology, drug targets and disease mechanism.
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