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Effects of Tangluo Ning on apoptosis and MAPKs signaling pathway of rat dorsal root ganglion neurons in high glucose environment#br# |
ZHU Yufei1 GUO Yuxin1 WANG Liying2 LI Jin1 ZHANG Taojing2 |
1.The Second Clinical Medical College, Beijing University of Chinese Medicine, Beijing 100029, China;
2.Department of Endocrinology, Dongfang Hospital, Beijing University of Chinese Medicine, Beijing 100078, China |
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Abstract Objective To study the effect of Tangluo Ning on apoptosis and mitogen-activated protein kinases (MAPKs) signaling pathway of rat dorsal root ganglion neurons (DRGn) in high glucose environment. Methods Sixty clean grade male SD rats with body weight of (215±15) g at 6-8 weeks were divided into high, medium, and low concentration glucolonin groups and normal group according to random number table method, with 15 rats in each group. Each group was given 5, 2.5, 1.25 g/(kg·d) crude medicine of Tangluo Ning prescription and equal amount of distilled water intragastric administration to prepare drug-containing serum and normal control serum. DRGn cells were prepared from newborn SD fetal rats and were divided into normal group (10% normal rat serum +Neurobasal medium), high glucose group (based on normal group +50 mmol/L glucose), and Tangluo Ning concentration groups (based on high glucose group +10% low, medium, and high concentration Tangluo Ning drug-containing serum). Cell apoptosis and protein expression of JNK1, p-JNK1, c-Jun, p-c-Jun, Map3k8, and p-Map3k8 were detected after 24 h culture. Results The apoptosis rate, expression of p-JNK1, p-c-Jun, Map3k8, and p-Map3k8 and ratio of p-JNK1/JNK1, p-c-Jun/c-Jun, and p-Map3k8/Map3k8 in high glucose group were higher than those in normal group, the differences were statistically significant (P < 0.05 or P < 0.01). The apoptosis rate, expression of p-JNK1, p-c-Jun, and p-Map3k8 and ratio of p-JNK1/JNK1, p-c-Jun/c-Jun, and p-Map3k8/Map3k8 in Tangluo Ning concentration groups were significantly lower than those in high glucose group, the differences were highly statistically significant (P < 0.01). Apoptosis rate, expression of p-JNK1, p-c-Jun, and p-Map3k8 and ratio of p-JNK1/JNK1, p-c-Jun/c-Jun, and p-Map3k8/Map3k8 in middle concentration Tangluo Ning group were significantly lower than those in high and low concentration Tangluo Ning group, the differences were statistically significant (P < 0.01 or P < 0.05). The expression of c-Jun in the medium and low concentration Tangluo Ning groups was lower than that in the high concentration Tangluo Ning group, and the differences were statistically significant (P < 0.05). There was no significant difference in the expression of JNK1, Map3k8 and c-Jun in the Tangluo Ning concentration groups (P > 0.05). Conclusion Tangluo Ning can reduce apoptosis by inhibiting MAPKs signaling pathway.
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[1] Pouya S,Inga P,Paraskevi S,et al. Global and regional diabetes prevalence estimates for 2019 and projections for 2030 and 2045:Results from the International Diabetes Federation Diabetes Atlas,9th edition [J]. Diabetes Res Clin Pract,2019,157:107843.
[2] Witzel II,Jelinek HF,Khalaf K,et al. Identifying Common Genetic Risk Factors of Diabetic Neuropathies [J]. Front Endocrinol,2015,6:88.
[3] 方朝晖,吴以岭,赵进东.糖尿病周围神经病变中医临床诊疗指南(2016年版)[J].中医杂志,2017,58(7):625-630.
[4] Mao W,Yip CW,Chen W. Complications of diabetes in China:health system and economic implications [J]. BMC Public Health,2019,19(1):269.
[5] 袁玉松,徐海林,芦浩,等.糖尿病周围神经病变研究进展[J].中华肩肘外科电子杂志,2019,7(1):87-92.
[6] 黄海伦,吴珊.糖尿病周围神经病相关发病机制研究进展[J].中华脑科疾病与康复杂志:电子版,2019,9(3):176-180.
[7] 段秋婷,周晋宇,尹冶,等.lncRNA和microRNA在糖尿病中的研究进展[J].重庆医学,2020,49(6):1012-1017.
[8] Jia L,Wang L,Chopp M,et al. MiR-29c/PRKCI Regulates Axonal Growth of Dorsal Root Ganglia Neurons Under Hyperglycemia [J]. Mol Neurobiol,2018,55(1):851-858.
[9] Liu W,Liang Xc,Shi Y. Effects of Hirudin on High Glucose-Induced Oxidative Stress and Inflammatory Pathway in Rat Dorsal Root Ganglion Neurons [J]. Chin J Integr Med,2020,26(3):197-204.
[10] 李娜,王利莹,李逸潇,等.糖络宁对高糖环境下大鼠背根神经节神经元细胞氧化应激及PI3K/AKT信号通路的影响[J].北京中医药,2020,39(11):1161-1165.
[11] 刘琴.基于miRNA-200a探讨糖络宁改善高糖下大鼠背根神经元氧化应激机制[D].北京:北京中医药大学,2020.
[12] 孙青,梁晓春,张宏.胚胎大鼠背根神经节神经元的原代培养[J].医学研究杂志,2016,45(1):66-68.
[13] 吴亚楠,梁晓春,杨丹,等.筋脉通含药血清对高糖培养SD大鼠背根神经元NADPH氧化酶p47~(phox)亚基及NT表达的影响[J].中华中医药杂志,2019,34(4):1440-1443.
[14] 李逸潇,王利莹,郭宇鑫,等.糖络宁对糖尿病周围神经病变大鼠背根神经节Toll样受体2/4的影响[J].中国医药导报,2020,17(13):37-40.
[15] 刁铁成.糖尿病周围神经病变中医诊治25例分析[J].糖尿病新世界,2016,19(12):107-108.
[16] 陈枫,郭宇鑫,王利莹,等.糖络宁对糖尿病周围神经病变大鼠细胞凋亡相关通路的影响[J].中国医药导报,2020,17(29):21-24.
[17] 李潇,姚伟洁,杨鑫伟,等.糖络宁对糖尿病周围神经病变大鼠坐骨神经功能及内质网应激IRE1α-XBP-1-CHOP通路的影响[J].湖南中医药大学学报,2019,39(7):841-847.
[18] 朱笳悦,姚伟洁,许利平,等.糖络宁含药血清对高糖环境下RSC96细胞Keap1/Nrf2/Bcl-2途径的作用机制研究[J].北京中医药,2019,38(2):106-113.
[19] 郝红,李方,王志,等.隐丹参酮对脑缺血再灌注损伤神经元细胞凋亡的作用[J].中国临床药理学杂志,2021, 37(3):250-254.
[20] 于竹芹,汪贯习,王潇璐,等.胡黄连苷Ⅱ干预脑缺血/再灌注损伤后p38丝裂原活化蛋白激酶信号通路的作用机制[J].解剖学报,2021,52(2):196-204.
[21] 祝盼盼,商亚珍.MAPK信号通路介导细胞凋亡的研究进展[J].承德医学院学报,2021,38(3):243-246.
[22] 田芳,王鹏,孙萍,等.四逆汤对慢性肾功能衰竭大鼠尿酸水平及p38 MAPK/ERK1/2信号通路的影响[J].疑难病杂志,2021,20(12):1257-1262.
[23] 赵淦琳炜,杨毅.p38MAPK信号通路参与BMP2诱导MSCs的归巢效应研究[J].中国临床研究,2020,33(4):437-441.
[24] Zhe Q,Zong YZ,Ting P,et al. Inhibition of TPL2 by interferon-α suppresses bladder cancer through activation of PDE4D [J]. J Exp Clin Cancer Res,2018,37(1):288.
[25] 郑书国,朱元美,陶善珺,等.丹酚酸B对间歇性高糖诱导的JNK活化和INS-1细胞凋亡的影响[J].中国药理学通报,2017,33(1):68-73.
[26] 李林,徐长水,张平,等.ERK磷酸化对糖尿病周围神经病雪旺氏细胞Netrin-1表达水平及凋亡的影响[J].卒中与神经疾病,2020,27(4):430-434.
[27] 孙石柱,王璐璐,姚立杰,等.BCA-1通过ErK信号通路促进高糖环境下人脂肪间充质干细胞增殖和迁移[J].中国医药科学,2020,10(19):28-32.
[28] 余冬梅,安输,杨洋,等.JNK激酶在细胞凋亡中的作用及其与癌症的关系[J].中国药理学通报,2015,31(12):1641-1645. |
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