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5-羟色胺在心肌梗死和/或抑郁大鼠模型的不同预处理下的变化。

5-Hydroxytryptamine Changes under Different Pretreatments on Rat Models of Myocardial Infarction and/or Depression.

机构信息

Department of Cardiology, Beijing Anzhen Hospital, Capital Medical University, Beijing 100029, China.

Department of Neurosciences, Allegheny College, Meadville 16335, USA.

出版信息

Chin Med J (Engl). 2017 Sep 20;130(18):2219-2225. doi: 10.4103/0366-6999.213966.

DOI:10.4103/0366-6999.213966
PMID:28875958
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5598335/
Abstract

BACKGROUND

: Psychocardiological researches have suggested a central role of 5-hydroxytryptamine (5-HT) on psychocardiological mechanism. This study aimed to further explore the central role of 5-HT and pretreatment effects of XinLingWan on rats with myocardial infarction (MI) and/or depression.

METHODS

: Ninety Sprague-Dawley rats were randomly divided into three groups: MI group, depression group, and MI + depression group (n = 30 in each group). Each group was then divided into three subgroups (n = 10 in each subgroup): a negative control subgroup (NCS), a Western medicine subgroup (WMS), and a traditional Chinese medicine subgroup (TCMS), which were received pretreatment once a day for 4 weeks by saline, 20 mg/kg sertraline mixed with 2 ml saline, and 40 mg/kg XingLingWan mixed with 2 ml saline, respectively. Different rat models were established after different pretreatments. Rats were then sacrificed for detection of serum 5-HT, platelet 5-HT, 5-HT receptors (5-HTR), and serotonin transporter (SERT). Data were analyzed by one-way analysis of variance (ANOVA) and least-significant difference (LSD) testing.

RESULTS

: MI group: compared with NCS, there was a significant increase in WMS and TCMS of serum 5-HT (176.15 ± 11.32 pg/ml vs. 334.50 ± 29.09 pg/ml and 474.04 ± 10.86 pg/ml, respectively, both P = 0.000), platelet 5-HT (129.74 ± 27.17 pg/ml vs. 322.24 ± 11.60 pg/ml and 340.4 5 ± 17.99 pg/ml, respectively, both P = 0.000); depression group: compared with NCS, there was a significant increase in WMS and TCMS of serum 5-HT (194.69 ± 5.09 pg/ml vs. 326.21 ± 39.98 pg/ml and 456.33 ± 23.12 pg/ml, respectively, both P = 0.000), platelet 5-HT (175.15 ± 4.07 pg/ml vs. 204.56 ± 18.59 pg/ml and 252.03 ± 22.26 pg/ml, respectively, P = 0.004 and P = 0.000, respectively); MI + depression group: compared with NCS, there was a significant increase in both WMS and TCMS of serum 5-HT (182.50 ± 10.23 pg/ml vs. 372.55 ± 52.23 pg/ml and 441.76 ± 23.38 pg/ml, respectively, both P = 0.000) and platelet 5-HT (180.83 ± 11.08 pg/ml vs. 221.12 ± 22.23 pg/ml and 265.37 ± 29.49 pg/ml, respectively, P = 0.011 and P = 0.000, respectively).

CONCLUSIONS

: By elevating the amount of 5-HT and modulating 5-HTR and SERT levels in serum and platelets, XinLingWan and sertraline were found to exert pretreatment effect on rat models of MI and/or depression.

摘要

背景

心理心脏病学研究表明,5-羟色胺(5-HT)在心理心脏病学机制中起核心作用。本研究旨在进一步探讨 5-HT 的核心作用,以及心宁丸预处理对心肌梗死(MI)和/或抑郁症大鼠的影响。

方法

90 只 Sprague-Dawley 大鼠随机分为三组:MI 组、抑郁组和 MI+抑郁组(每组 30 只)。每组又分为三个亚组(每组 10 只):阴性对照组(NCS)、西药组(WMS)和中药组(TCMS),分别给予生理盐水、20mg/kg 舍曲林混合 2ml 生理盐水和 40mg/kg 心宁丸混合 2ml 生理盐水每日预处理 1 次,共 4 周。在不同的预处理后建立不同的大鼠模型。然后处死大鼠,检测血清 5-HT、血小板 5-HT、5-HT 受体(5-HTR)和血清素转运蛋白(SERT)。采用单因素方差分析(ANOVA)和最小显著差异(LSD)检验进行数据分析。

结果

MI 组:与 NCS 相比,WMS 和 TCMS 的血清 5-HT 水平显著升高(176.15±11.32pg/ml 比 334.50±29.09pg/ml 和 474.04±10.86pg/ml,均 P=0.000),血小板 5-HT 水平也显著升高(129.74±27.17pg/ml 比 322.24±11.60pg/ml 和 340.45±17.99pg/ml,均 P=0.000);抑郁组:与 NCS 相比,WMS 和 TCMS 的血清 5-HT 水平显著升高(194.69±5.09pg/ml 比 326.21±39.98pg/ml 和 456.33±23.12pg/ml,均 P=0.000),血小板 5-HT 水平也显著升高(175.15±4.07pg/ml 比 204.56±18.59pg/ml 和 252.03±22.26pg/ml,P=0.004 和 P=0.000);MI+抑郁组:与 NCS 相比,WMS 和 TCMS 的血清 5-HT 水平均显著升高(182.50±10.23pg/ml 比 372.55±52.23pg/ml 和 441.76±23.38pg/ml,均 P=0.000),血小板 5-HT 水平也显著升高(180.83±11.08pg/ml 比 221.12±22.23pg/ml 和 265.37±29.49pg/ml,P=0.011 和 P=0.000)。

结论

通过升高 5-HT 的含量,调节血清和血小板中 5-HTR 和 SERT 的水平,心宁丸和舍曲林对 MI 和/或抑郁症大鼠模型具有预处理作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/442e/5598335/13a24053f57a/CMJ-130-2219-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/442e/5598335/42d714488dc7/CMJ-130-2219-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/442e/5598335/7ee758d586e5/CMJ-130-2219-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/442e/5598335/ebc1f8f2c0cb/CMJ-130-2219-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/442e/5598335/13a24053f57a/CMJ-130-2219-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/442e/5598335/42d714488dc7/CMJ-130-2219-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/442e/5598335/7ee758d586e5/CMJ-130-2219-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/442e/5598335/ebc1f8f2c0cb/CMJ-130-2219-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/442e/5598335/13a24053f57a/CMJ-130-2219-g004.jpg

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