Traditional Chinese Medicine
Vol. 08  No. 02 ( 2019 ), Article ID: 29197 , 8 pages
10.12677/TCM.2019.82022

Clinical Observation of Danshen Ligustrazine Injection in the Treatment of aPL Positive Recurrent Spontaneous Abortion

Sanshan Jin1, Yingchun Zhang2*

1First Clinical Medical College, Hubei University of Chinese Medicine, Wuhan Hubei

2Maternal and Child Health Hospital of Hubei Province, Wuhan Hubei

Received: Feb. 15th, 2019; accepted: Mar. 4th, 2019; published: Mar. 11th, 2019

ABSTRACT

Objective: To observe the efficacy and safety of Danshen Ligustrazine Injection (DLI) in aPL-positive recurrent abortion women. Methods: 180 cases of selected outpatients were included in this experiment: 90 cases in the control group and 90 cases in the treatment group. Blood D-dimer (D-Di), platelet aggregation rate (PAR) and uterine artery RI and PI values of patients in the control group (heparin + dydrogesterone + folic acid) and the treatment group (DLI + heparin + dydrogesterone + folic acid) were detected. And the live birth rate, preterm birth rate and other adverse events were observed and calculated. Results: The overall live birth rate of the treatment group was higher than that of the control group (P < 0.05). The incidence of preeclampsia, vaginal bleeding and drug-induced liver injury in the treatment group was lower than that in the control group (P < 0.05). There was no significant difference in the incidence of premature birth rate and fetal malformation between the two groups (P > 0.05). D-Di, platelet aggregation rate, bilateral uterine artery RI, and PI values showed a downward trend after treatments in two groups, but the treatment group showed a more significant decrease (P < 0.05). Conclusion: DLI can improve the hypercoagulability of patients, improve the uterine hemodynamics during pregnancy, promote the maintenance of pregnancy, increase the live birth rate, and reduce the incidence of pre-pregnancy. In combination with heparin, it can enhance heparin anti-coagulation and anti-abortion effects, reduce the incidence of heparin drug-induced liver injury and does not increase the incidence of adverse events, such as premature delivery, fetal malformation and vaginal bleeding. The medication during pregnancy is safe and effective.

Keywords:Traditional Chinese Medicine, Danshen Ligustrazine Injection, Recurrent Spontaneous Abortion, Low Molecular Weight Heparin

丹参川芎嗪针治疗aPL阳性复发性流产的临床观察

金三珊1,张迎春2*

1湖北中医药大学,第一临床医学院,湖北 武汉

2湖北省妇幼保健院,中医科,湖北 武汉

收稿日期:2019年2月15日;录用日期:2019年3月4日;发布日期:2019年3月11日

摘 要

目的:观察丹参川芎嗪针对aPL阳性复发性流产女性中的保胎疗效及安全性。方法:收集有效门诊病历180例;对照组与治疗组各90例,观察对照组(肝素 + 地屈孕酮 + 叶酸干预)与治疗组(在对照组基础上加用丹参川芎嗪针)患者血D二聚体(D-Di)、血小板聚集率及患者双侧子宫动脉RI、PI指标变化,并通过回访了解各组活产率、早产率及其它不良事件发生率。结果:治疗组总体活产率高于对照组(P < 0.05)。治疗组子痫前期、阴道出血发生率及药物性肝损伤发生概率低于对照组(P < 0.05)。两组早产率、胎儿畸形发生率无统计学意义(P > 0.05)。两组治疗后D-Di、血小板聚集率、双侧子宫动脉RI、PI值均呈下降趋势,且治疗组下降更明显(P < 0.05)。结论:丹参川芎嗪针能改善患者高血凝状态,改善患者妊娠期子宫血流动力学指标,促进妊娠的维持,增加活产率,降低子痫前期的发生。配合肝素使用,增强肝素抗凝及保胎作用,减轻肝素药物性肝损伤发生概率,不增加早产、胎儿畸形、阴道出血不良事件发生率。孕期用药安全性高。

关键词 :中药,丹参川芎嗪针,复发流产,低分子肝素

Copyright © 2019 by author(s) and Hans Publishers Inc.

This work is licensed under the Creative Commons Attribution International License (CC BY).

http://creativecommons.org/licenses/by/4.0/

1. 引言

发生连续2次及以上的自然流产,称为复发性流产(RSA),其病因病机复杂,育龄期妇女发病率达1%~3% [1] 。抗磷脂抗体(antiphospholipid antibodies aPL)是一组异质性的自身抗体,可在0%~5%人群被中检出 [1] [2] ,它与复发性流产、死胎 [3] [4] [5] [6] [7] 、先兆子痫、胎儿宫内生长受限、早产 [4] [7] [8] [9] [10] 、动静脉血栓形成 [11] [12] [13] [14] 等疾病发生有关。其中超过40%的女性可出现复发性流产、死胎 [3] [4] [5] [6] [7] 。aPL能与β2糖蛋白(β2-GPI) [15] 结合,激活血小板,损伤血管内皮,激活补体系统,促进大量促凝因子的产生、胎盘血管血栓的形成,导致流产、妊娠期子痫前状态的发生。抗凝抗血小板药成为治疗APS复发性流产的重要药物。基于凝血亢进与APS不良妊娠间的联系,及丹参川芎嗪针的改善血供及组织代谢的药理作用,我们展开了对丹参川芎嗪针对aPL阳性复发性流产患者妊娠结局影响的临床研究。

2. 资料与方法

2.1. 资料

2.1.1. 一般资料

收集2014年3月至2017年3月首次就诊我科的有连续流产2次及以上流产经历的女性共180人;其中流产2次者100人;流产3次者60人;流产4次及以上者20人。通过随机数字法将其随机均分入对照组及治疗组中。本研究2013年得到机构伦理委员会的道德批准,所有参与本研究的女性均获得知情同意。

2.1.2. 纳入标准

1) 符合第8版《妇产科学》及中华医学会妇产科学分会2016年发布的RSA诊治指南中相关标准;2) 具有以下一项及以上指标阳性:D-二聚体(D-Di) > 0.5 mg/L,抗心磷脂抗体(anticardiolipin antibody, ACA)阳性,抗β2糖蛋白(β2GP-I)阳性,狼疮抗凝物(LA)阳性,血小板聚集率(PAgT) > 69%。

2.1.3. 排除标准

1) 夫妇双方有一方及以上染色体异常;2) 男方精液常规异常;3) 有肝素使用禁忌症者;或因早孕反应严重服药困难者。4) 有子宫畸形,宫腔粘连、子宫肌瘤、子宫内膜异位症及盆腔炎者。5) 排除内分泌疾病:糖尿病、甲亢等内分泌疾病患者。除ACA、β2GP-I、LA外有其它自身抗体阳性者。6) 有生殖道急性感染者。7) 夫妻双方一方及以上具有抽烟或酗酒史。

2.2. 方法

2.2.1. 治疗方法

从备孕前3个月开始,所有受试对象开始常规服用叶酸400 μg/d;自B超确定宫内妊娠起,两组均口服地屈孕酮片(苏威制药生产) l0 mgpo bid;并予低分子肝素(葛兰素史克有限公司) 4100IU IH q12h;治疗组在对照组基础上加用5%葡萄糖250 ml配丹参川芎嗪3 mlivgttqd。一般患者常规保胎至12周,若患者D-Di、凝血功能等指标检测项目恢复正常,胎儿生长发育良好,与孕周相符,患者未出现阴道流血、腰酸腹痛症状可考虑提前停药,停药后仍每月复查凝血指标及胎儿B超,必要时重新用药。

2.2.2. 监测指标

所有受试者规律检测排卵,排卵同房后10日每日抽血检查βHCG,判断患者是否妊娠。从确定妊娠后放入D1天开始用药,患者用药后每14 d空腹测查血清D-Di浓度、肝功能指标,血小板聚集率;盆腔B超检查患者双侧子宫动脉RI、PI值。治疗期间记录患者不良反应。并通过回访了解各组活产率、早产率及其它不良事件发生率。

2.2.3. 统计方法

采用SPSS22.0进行数据统计分析,计量资料以x ± s表示,治疗前后比较采用配对t检验;组间比较采用随机区组设计方差分析,并用SNK-q法进行多个样本均数之间的两两比较。计数资料用百分比表示,组间比较采用卡方检验,所有实验均以P < 0.05为水准进行统计学分析。重复检测资料采用拟合广义线性混合效应模型(MIXED)进行统计学分析。

3. 结果

比较孕前、孕4周、孕8周、孕12周患者血液各指标的变化。实验过程中治疗组缺失2人,对照组缺失1人。

3.1. 凝血指标

3.1.1. 血D-Di水平变化

图1所示,相同孕周治疗组与对照组各指标进行比较,重复检测资料通过拟合广义线性混合效应模型(MIXED)进行统计学分析。药物干预后,对照组与治疗组D-Di平均值均呈下降趋势(时间P < 0.05),且治疗组的下降趋势较对照组更明显(处理因素P < 0.01)。

注:*P < 0.05,**P < 0.01,***P < 0.001,****P < 0.0001。

Figure 1. Comparison of D-Di blood level between the treatment group and the control group

图1. 治疗组、对照组D-Di含量比较

3.1.2. 血液血小板聚集率变化

图2所示,相同孕周治疗组与对照组各指标进行比较,重复检测资料通过拟合广义线性混合效应模型(MIXED)进行统计学分析。药物干预后,对照组与治疗组血小板聚集率平均值均呈下降趋势(时间P < 0.05),且治疗组的下降趋势较对照组更明显(处理因素P < 0.05)。

注:*P < 0.05,**P < 0.01,***P < 0.001,****P < 0.0001。

Figure 2. Comparison of platelet aggregation rate between the treatment group and the control group

图2. 治疗组、对照组血小板聚集率含量比较

3.2. 子宫动脉血流参数指标

3.2.1. 子宫动脉RI值变化

图3所示,相同孕周治疗组与对照组各指标进行比较,重复检测资料通过拟合广义线性混合效应模型(MIXED)进行统计学分析。药物干预后,对照组与治疗组子宫动脉RI平均值值均呈下降趋势(时间P < 0.01),且治疗组的下降趋势较对照组更明显(处理因素P < 0.01)。

注:*P < 0.05,**P < 0.01,***P < 0.001,****P < 0.0001。RI值取双侧子宫动脉的平均值。

Figure 3. Comparison of uterine artery RI value between the treatment group and the control group

图3. 治疗组、对照组子宫动脉RI值比较

3.2.2. 子宫动脉PI值变化

图4所示,相同孕周治疗组与对照组各指标进行比较,重复检测资料通过拟合广义线性混合效应模型(MIXED)进行统计学分析。药物干预后,对照组与治疗组子宫动脉PI平均值值均呈下降趋势(时间P < 0.01),且治疗组的下降趋势较对照组更明显(处理因素P < 0.01)。

注:RI、PI值均取双侧子宫动脉的平均值。

注:*P < 0.05,**P < 0.01,***P < 0.001 ****P < 0.0001。PI值取双侧子宫动脉的平均值。

Figure 4. Comparison of uterine artery PI value between the treatment group and the control group

图4. 治疗组、对照组子宫动脉PI值比较

3.3. 活产率及不良事件发生率

3.3.1. 畸形发生率

两组观察病例中均未及有明显胎儿外观及超声下畸形者。

3.3.2. 活产、早产、子痫前期、阴道出血、药物性肝损伤发生率

表1所示,治疗组活产率明显高于对照组(P < 0.05);早产率、畸胎发生率间无明显差异(P > 0.05);治疗组较对照组子痫前期、阴道出血及药物性肝损伤发生率明显低于对照组(P < 0.05)。

4. 讨论

目前抗凝、抗血小板药仍是治疗APS复发性流产的主要药物。低分子肝素被证实是治疗APS复发性流产的有效药物 [16] [17] [18] ,肝素单独或联合小剂量阿司匹林是血栓前状态复发性流产的一线治疗方案 [19] [20] 。

Table 1. Live birth, premature delivery, preeclampsia, vaginal bleeding, drug-induced liver injury rates between the treatment group and the control group

表1. 治疗组与对照组活产、早产、子痫前期、阴道出血、药物性肝损伤发生率的比较

然而仍有近30% [21] 的女性对单纯抗凝治疗缺乏敏感。中药及中成药的开发运用逐渐受到人们的关注。丹参川芎嗪针从传统中药丹参及川芎中提取而来,主要药效成分为丹参素及盐酸川芎嗪。研究表明丹参中的有效成分丹参素具有保护血管内皮细胞 [22] 、减轻内皮炎症损伤 [23] 、抗脂质过氧化 [24] 、改善微循环、清除氧自由基 [25] [26] 、改善血循环中红细胞的聚集现象、减少血流阻力 [27] 的作用。川芎嗪是一种TXA2 (血栓烷A2)合成酶抑制剂,具有抑制血小板磷脂酶A2活性、减少内源性花生四烯酸的释放及TXA2的合成,从而抑制血小板激活的作用 [27] 。川芎嗪还通过抑制炎症信号通路的激活 [28] ,减轻炎症介导的组织损伤。同时川芎嗪还具有抗血栓形成 [29] [30] 、保护血管内皮细胞 [31] 的作用,这些都有利于改善病变组织的血供。

丹参川芎嗪针因具有改善组织血供,促进组织代谢,安全,高效而被广泛用于多种血瘀性疾病的治疗。丹参川芎嗪针在心脑血管疾病中的研究较多,然而在aPL阳性复发性流产中的临床运用相关研究较少。观察丹参川芎嗪针在aPL阳性所致复发性流产女性中的保胎疗效及安全性对拓展丹参川芎嗪针的临床适用范围具有重要的意义。

本实验通过临床研究发现,丹参川芎嗪针能改善aPL阳性患者高血凝状态,增加患者妊娠期子宫胎盘血供,以促进妊娠的维持,增加aPL阳性患者活产率,降低子痫前期发生率。配合肝素使用,能增强肝素抗凝作用,减轻肝素药物性肝损伤发生概率,不增加早产、胎儿畸形、阴道出血等不良事件发生率,孕期用药安全性高。丹参川芎嗪注射液在心脑血管上的运用历史悠久、价格低廉。相较肝素皮下注射方式,丹参川芎嗪针的静脉注射方式对患者造成的痛苦更小,接受度更高,是治疗血栓前状态复发性流产的潜力药。然而丹参川芎嗪注射液在血栓前状态复发性流产的运用处于初始阶段,还需要更多临床及实验研究进一步证实其孕期用药的安全性及治疗的有效。

基金项目

湖北省卫生计生委联合创新团队项目,WJ2018H0135;湖北省卫生计生委基金重点项目,2017Z-Z09;湖北省卫生计生委基金一般项目,2013Z-Y15。

文章引用

金三珊,张迎春. 丹参川芎嗪针治疗aPL阳性复发性流产的临床观察
Clinical Observation of Danshen Ligustrazine Injection in the Treatment of aPL Positive Recurrent Spontaneous Abortion[J]. 中医学, 2019, 08(02): 120-127. https://doi.org/10.12677/TCM.2019.82022

参考文献

  1. 1. D’Cruz, D.P. (2006) Antiphospholipid (Hughes) Syndrome: An Overview. In: Khamashta, M.A., Ed., Huges Syn-drome, Springer-Verlag, London, 9-21. https://doi.org/10.1007/1-84628-009-5_2

  2. 2. Pattison, N.S., Chamley, L.W., McKay, E.J., Liggins, G.C. and Butler, W.S. (1993) Antiphospholipid Antibodies in Pregnancy: Prevalence and Clinical Associations. British Journal of Obstetrics and Gynaecology, 100, 909-913. https://doi.org/10.1111/j.1471-0528.1993.tb15105.x

  3. 3. Birdsall, M., Pattison, N. and Chamley, L. (1992) Antiphospholipid Antibodies in Pregnancy. Australian and New Zealand Journal of Obstetrics and Gynaecology, 32, 328-330. https://doi.org/10.1111/j.1479-828X.1992.tb02844.x

  4. 4. Lockwood, C.J., Romero, R., Feinberg, R.F., Clyne, L.P., Coster, B. and Hobbins, J.C. (1989) The Prevalence and Biologic Significance of Lupus Anticoagulant and Anticardiolipin Antibodies in a General Obstetric Population. American Journal of Obstetrics & Gynecology, 161, 369-373. https://doi.org/10.1016/0002-9378(89)90522-X

  5. 5. Petri, M. (2006) Epidemiology of Antiphospholipid Antibody Syndrome. In: Khamashta, M.A., Ed., Huges Syndrome, Springer-Verlag, London, 22-28. https://doi.org/10.1007/1-84628-009-5_3

  6. 6. Rai, R.S., Clifford, K., Cohen, H. and Regan, L. (2005) High Prospective Fetal Loss Rate in Untreated Pregnancies of Women with Recurrent Miscarriage and Antiphospholipid Antibodies. Human Reproduction, 10, 3301-3304. https://doi.org/10.1093/oxfordjournals.humrep.a135907

  7. 7. Yasuda, M., Takakuwa, K., Tokunaga, A. and Tanaka, K. (1995) Prospective Studies of the Association between Anticardiolipin Antibody and Outcome of Pregnancy. Obstetrics & Gynecology, 86, 555-559. https://doi.org/10.1016/0029-7844(95)00247-O

  8. 8. Allen, J.L., Tapia-Santiago, C. and Kutteh, W.H. (1996) Antiphospholipid Antibodies in Patients with Preeclampsia. American Journal of Reproductive Immunology, 36, 81-85. https://doi.org/10.1111/j.1600-0897.1996.tb00143.x

  9. 9. Branch, D.W.M., Andres, R.M., Digre, K.B.M., Rote, N.S.P. and Scott, J.R.M. (1989) The Association of Antiphospholipid Antibodies with Severe Preeclampsia. Obstetrics & Gynecology, 73, 541-545.

  10. 10. Katano, K., Aoki, K., Sasa, H., Ogasawara, M., Matsuura, E. and Yagami, Y. (1996) Beta 2-Glycoprotein I-Dependent Anticardiolipin Antibodies as a Predictor of Adverse Pregnancy Outcomes in Healthy Pregnant Women. Human Reproduction, 11, 509-512. https://doi.org/10.1093/HUMREP/11.3.509

  11. 11. Harris, E., Chan, J.H., Asherson, R.A., Aber, V.R., Gharavi, A.E. and Hughes, G.V. (1986) Thrombosis, Recurrent Fetal Loss, and Thrombocytopenia: Predictive Value of the Anticardiolipin Antibody Test. Archives of Internal Medicine, 146, 2153-2156. https://doi.org/10.1001/archinte.1986.00360230069012

  12. 12. Harris, E.N., Boey, M.L., Mackworth-Young, C.G., Gharavi, A.E., Patel, B.M., Loizou, S. and Hughes, G.R.V. (1983) Anticardiolipin Antibodies: Detection by Radioimmunoassay and Association with Thrombosis in Systemic Lupus Erythematosus. The Lancet, 322, 1211-1214. https://doi.org/10.1016/S0140-6736(83)91267-9

  13. 13. Reynaud, Q., Lega, J., Mismetti, P., Chapelle, C., Wahl, D., Cathébras, P. and Laporte, S. (2014) Risk of Venous and Arterial Thrombosis according to Type of Antiphospholipid Antibodies in Adults without Systemic Lupus Erythematosus: A Systematic Review and Meta-Analysis. Autoimmunity Reviews, 13, 595-608. https://doi.org/10.1016/j.autrev.2013.11.004

  14. 14. Wahl, D., Guillemin, F., de Maistre, E., Perret-Guillaume, C., Lecompte, T. and Thibaut, G. (1998) Meta-Analysis of the Risk of Venous Thrombosis in Individuals with Antiphospholipid Antibodies without Underlying Autoimmune Disease or Previous Thrombosis. Lupus, 7, 15-22. https://doi.org/10.1191/096120398678919688

  15. 15. Cabral, A.R., Cabiedes, J. and Alarcón-Segovia, D. (2004) Heterogeneity of Antibodies to Beta2-Glycoprotein 1 from Patients with Systemic Lupus Erythematosus. Lupus, 13, 182-187. https://doi.org/10.1191/0961203303lu531oa

  16. 16. Jong, P.G.D., Quenby, S., Bloemenkamp, K.W., Braams-Lisman, B.A., de Bruin, J.P., Coomarasamy, A., David, M., DeSancho, M.T., van der Heijden, O.W., Hoek, A., Hutten, B.A., Jochmans, K., Koks, C.A., Kuchenbecker, W.K., Mol, B.W., Torrance, H.L., Scheepers, H.C., Stephenson, M.D., Verhoeve, H.R., Visser, J., de Vries, J.I., Goddijn, M. and Middeldorp, S. (2015) ALIFE2 Study: Low-Molecular-Weight Heparin for Women with Recurrent Miscarriage and Inherited Thrombophilia—Study Protocol for a Randomized Controlled Trial. Trials, 16, 208. https://doi.org/10.1186/s13063-015-0719-9

  17. 17. Check, J.H. (2012) The Use of Heparin for Preventing Miscarriage. American Journal of Reproductive Immunology, 67, 326-333. https://doi.org/10.1111/j.1600-0897.2012.01119.x

  18. 18. Fouda, U.M., Sayed, A.M., Abdou, A.M., Ramadan, D.I., Fouda, I.M. and Zaki, M.M. (2010) Enoxaparin versus Unfractionated Heparin in the Management of Recurrent Abortion Secondary to Antiphospholipid Syndrome. International Journal of Gynecology & Obstetrics, 112, 211-215. https://doi.org/10.1016/j.ijgo.2010.09.010

  19. 19. (2015) Correction to Dosage in: Antiplatelet Drugs: Antithrombotic Therapy and Prevention of Thrombosis: 9th Ed: American College of Chest Physicians Evidence-Based Clinical Practice Guidelines. Chest, 148, 1529.

  20. 20. Bouvier, S., Cochery-Nouvellon, E., GéraldineLavigne-Lissalde, G., Mercier, E., Marchetti, T., Balducchi, J.P., Marès, P. and Gris, J.C. (2013) Comparative Incidence of Pregnancy Outcomes in Treated Obstetric Antiphospholipid Syndrome: The NOH-APS Observational Study. Blood, 123, 404-413. https://doi.org/10.1182/blood-2013-08-522623

  21. 21. Bramham, K., Hunt, B.J., Germain, S., Calatayud, I., Khamashta, M., Bewley, S. and Nelson-Piercy, C. (2010) Pregnancy Outcome in Different Clinical Phenotypes of Antiphospholipid Syndrome. Lupus, 19, 58-64. https://doi.org/10.1177/0961203309347794

  22. 22. Zhao, Q.T., Guo, Q.M., Wang, P. and Wang, Q. (2012) Salvianic Acid a Inhibits Lipopolysaccharide-Induced Apoptosis through Regulating Glutathione Peroxidase Activity and Malondialdehyde Level in Vascular Endothelial Cells. Chinese Journal of Natural Medicines, 10, 53-57. https://doi.org/10.3724/SP.J.1009.2012.00053

  23. 23. 季亢挺, 唐疾飞, 陈鹏, 等. 丹参素保护内皮祖细胞炎症损伤的机制研究[J]. 中国预防医学杂志, 2010, 11(8): 809-812.

  24. 24. Zhang, J.P., Zhang, Y.Y., Zhang, Y., Gao, Y.G., Ma, J.J., Wang, N., Wang, J.Y., Xie, Y., Zhang, F.H. and Chu, L. (2013) Salvia Miltiorrhiza (Danshen) Injection Ameliorates Iron Overload-Induced Cardiac Damage in Mice. Planta Medica, 79, 744-752. https://doi.org/10.1055/s-0032-1328588

  25. 25. 边金铎, 邓同乐, 许健, 等. 丹参素对H2O2诱导的内皮细胞氧化损伤的保护作用研究[J]. 上海中医药大学学报, 2012, 25(3): 61-65.

  26. 26. 曹金仪. 丹参的化学成分及临床用途[J]. 中国医药指南, 2012, 10(29): 53-55.

  27. 27. 裴艳霞. 川芎的药理作用及临床应用[J]. 中国医药指南, 2011, 9(34): 197-198.

  28. 28. Wu, X.F., Zhang, F., Xiong, X., Lu, C., Lian, N., Lu, Y. and Zheng, S. (2015) Tetramethylpyrazine Reduces Inflammation in Liver Fibrosis and Inhibits Inflammatory Cytokine Expression in Hepatic Stellate Cells by Modulating NLRP3 Inflammasome Pathway. IUBMB Life, 67, 312-321. https://doi.org/10.1002/iub.1348

  29. 29. 杨文辉, 龚国清, 周怡, 等. 川芎嗪体内抗血栓活性及机制探究[J]. 中国临床药理学与治疗学, 2012, 17(3): 241-245.

  30. 30. Cai, X.X., Chen, Z., Pan, X.K., Xia, L., Chen, P., Yang, Y., Hu, H., Zhang, J., Li, K., Ge, J., Yu, K. and Zhuang, J. (2014) Inhibition of Angiogenesis, Fibrosis and Thrombosis by Tetramethylpyrazine: Mechanisms Contributing to the SDF-1/CXCR4 Axis. PLoS ONE, 9, e88176. https://doi.org/10.1371/journal.pone.0088176

  31. 31. Xu, Q., Xia, P., Li, X., Wang, W., Liu, Z. and Gao, X. (2014) Tetramethylpyrazine Ameliorates High Glucose-Induced Endothelial Dysfunction by Increasing Mitochondrial Biogenesis. PLoS ONE, 9, e88243. https://doi.org/10.1371/journal.pone.0088243

  32. NOTES

    *通讯作者。

期刊菜单