Protective effects of Zuogui Jiangtang Jieyu Formula on hippocampal neurons in rats of diabetes complicated with depression via the TRP/KYN metabolic pathway

Protective effects of Zuogui Jiangtang Jieyu Formula on hippocampal neurons in rats of diabetes complicated with depression via the TRP/KYN metabolic pathway
复制标题

左归降糖解郁方通过TRP/KYN代谢途径对糖尿病合并抑郁大鼠海马神经元的保护作用

DOI:
10.1016/j.dcmed.2022.06.010
复制
发表时间:
2022-06
影响因子:
--
通讯作者:
Wang Yuhong
Wang Yuhong
中科院分区:
--
文献类型:
--
作者:
Ling Jia;Liu Jian;Jin Shi;Zou Manshu;Jiang Yajie;Wang Yuhong

文献摘要

参考文献

相似文献

ObjectiveTo explore the protective effects and mechanism of Zuogui Jiangtang Jieyu Formula (左归降糖解郁方, ZGJTJYF) on hippocampal neurons in rats of diabetes complicated with depression (DD) via the TRP/KYN metabolic pathway.Methods(i)In vivoexperiments: 60 specified pathogen free (SPF) grade male Sprague-Dawley (SD) rats were randomly divided into six groups with 10 rats in each groups: control, DD model, positive (1.8 mg/kg fluoxetine + 0.18 g/kg metformin), high-dose ZGJTJYF (ZGJTJYF-H, 40.500 g/kg ZGJTJYF), middle-dose ZGJTJYF (ZGJTJYF-M, 20.250 g/kg ZGJTJYF), and low-dose ZGJTJYF (ZGJTJYF-L, 10.125 g/kg ZGJTJYF) groups. Except for the control group, other groups were established DD model by high-fat emulsion intake with single tail vein streptozotocin (STZ) and four weeks of chronic unpredictable mild stress (CUMS). All drug administration groups were treated by gavage during CUMS modeling, and the control and model groups were given equal amount of distilled water. After four weeks, the serum levels of blood glucose and glycosylated hemoglobin were measured to determine the hypoglycemic effect of ZGJTJYF. Moreover, the open field test and Morris water maze test were performed to evaluate the antidepressant effect of ZGJTJYF. Changes in 5-hydroxytryptamine (5-HT) level were detected via high-performance liquid chromatography with electrochemical detection (HPLC-ECD); the levels of tryptophan (TRP), kynurenine (KYN), and indoleamine 2,3-dioxygenase (IDO) in the hippocampus were detected using enzyme-linked immunosorbent assay (ELISA); the protein expression levels of synaptophysin (SYN) and postsynaptic density material-95 (PSD-95) were detected via immunohistochemistry (IHC); and the protein expression levels of N-methyl-D-aspartate receptor (NR) 2A and NR2B were detected using Western blot. (ii)In vitroexperiments: five SPF grade SD pregnant rats (E16 – 18) were used to obtain primary hippocampal neurons (Ne), six SD new-born rats were used to collected primary astrocytes (As) and microglia (MG), and to establish a Ne-As-MG co-culture system. All co-culture systems were divided into six groups: control (PBS), model [150 mmol/L glucose + 200 μmol/L corticosterone (G&P) + PBS], blank (G&P + blank serum), positive (G&P + positive drug-containing serum), ZGJTJYF (G&P + ZGJTJYF serum), and 1-methyl-D-tryptophan (1-MT, IDO inhibitor) (G&P + 1-MT) groups. After 18 h of intervention by corresponding treatment, immunofluorescence was used to analyze the protein expression levels of SYN, PSD-95, NR2A, and NR2B; ELISA was performed to measure the levels of interleukin (IL)-1β, IL-6, tumor necrosis factor (TNF)-α, and TRP/KYN metabolic pathway-related factors [TRP, KYN, kynurenine acid (KYNA), quinolinic acid (QUIN)].Results(i)In vivoexperimental results showed that ZGJTJYF-M and ZGJTJYF-L significantly improved the elevated blood glucose state of DD rats (P< 0.01 andP< 0.05, respectively); ZGJTJYF-H, ZGJTJYF-M, and ZGJTJYF-L increased their autonomous activity, learning, and memory ability (P< 0.01,P< 0.01, andP< 0.05, respectively). Moreover, the levels of 5-HT and TRP were significantly increased (P< 0.01), and the levels of KYN and IDO were significantly decreased in the hippocampus (P< 0.01) of rats after ZGJTJYF-M treatment. The protein expression levels of SYN and PSD-95 were significantly upregulated in hippocampal neurons (P< 0.01), while the abnormal activation of NR2A and NR2B was markedly inhibited in hippocampus (P< 0.05) of rats after ZGJTJYF-M treatment. (ii)In vitroexperimental results showed that …
微生物群-肠-脑轴参与慢性束缚应激:肠道和大脑中犬尿氨酸代谢途径的紊乱
DOI: 10.1080/19490976.2020.1869501
发表时间: 2021-01
期刊: Gut microbes
影响因子: 12.2
作者:
Deng Y;Zhou M;Wang J;Yao J;Yu J;Liu W;Wu L;Wang J;Gao R
通讯作者: Gao R
DOI: 10.1016/j.biopha.2018.03.070
发表时间: 2018-06
期刊: Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie
影响因子: --
作者:
A. Mallek;J. Movassat;S. Ameddah;Junjun Liu;N. Semiane;Ali Khalkhal;Y. Dahmani
通讯作者: A. Mallek;J. Movassat;S. Ameddah;Junjun Liu;N. Semiane;Ali Khalkhal;Y. Dahmani
DOI: 10.3390/molecules25030564
发表时间: 2020-01
期刊: Molecules
影响因子: 4.6
作者:
Masaru Tanaka;Zsuzsanna Bohár;L. Vécsei
通讯作者: Masaru Tanaka;Zsuzsanna Bohár;L. Vécsei
DOI: 10.1523/eneuro.0566-20.2021
发表时间: 2021-07-01
期刊: ENEURO
影响因子: 3.4
作者:
Amellem, Ingrid;Yovianto, Glen;Tashiro, Ayumu
通讯作者: Tashiro, Ayumu
DOI: 10.3389/fncel.2021.739411
发表时间: 2021
影响因子: 5.3
作者:
Wasilewski D;Villalba-Moreno ND;Stange I;Glatzel M;Sepulveda-Falla D;Krasemann S
通讯作者: Krasemann S