中国临床药理学与治疗学 ›› 2026, Vol. 31 ›› Issue (5): 691-699.doi: 10.12092/j.issn.1009-2501.2026.05.014
收稿日期:2025-02-11
修回日期:2025-04-28
出版日期:2026-05-26
发布日期:2026-06-02
通讯作者:
邢维鑫,牟青春
E-mail:zengkang32@163.com;xingweixin1996@qq.com;muq@hainmc.edu.cn
作者简介:曾亢,男,硕士,硕士研究生在读,研究方向:脑卒中。E-mail:基金资助:
Kang ZENG1(
), Weixin XING2,*(
), Qingchun MU1,*(
)
Received:2025-02-11
Revised:2025-04-28
Online:2026-05-26
Published:2026-06-02
Contact:
Weixin XING,Qingchun MU
E-mail:zengkang32@163.com;xingweixin1996@qq.com;muq@hainmc.edu.cn
摘要:
缺血性疾病(ischemia)主要累及血供丰富的实质性器官(如心、脑、肝、肾、肺),在胃肠道等空腔脏器中亦具有较高发病率。广藿香醇(patchouli alcohol,PA)作为中国传统药用植物的活性成分,经多领域研究证实,其在心脑血管缺血、消化道缺血及相关缺血性疾病防治中展现出显著的保护效能,可有效延缓缺血病理进程。现有研究揭示,PA主要通过三种协同机制发挥缺血保护作用:(1)调控炎症反应级联;(2)清除氧化应激产物;(3)舒张血管平滑肌以改善血流灌注。这种多靶点干预策略使其在器官保护领域具有独特优势。本综述系统性阐释PA对多器官缺血损伤的治疗作用及分子机制,加深对传统中药活性成分的现代药理认知,提示其作为新一代缺血性疾病治疗药物的研发潜力。值得注意的是,PA的多靶点调控特性为创新药物设计提供了重要参考,有望突破单一作用机制药物的局限性,推动抗缺血治疗策略的革新。
中图分类号:
曾亢, 邢维鑫, 牟青春. 广藿香醇在治疗缺血相关疾病的研究进展[J]. 中国临床药理学与治疗学, 2026, 31(5): 691-699.
Kang ZENG, Weixin XING, Qingchun MU. Research progress of patchouli alcohol in the treatment of ischemia-related diseases[J]. Chinese Journal of Clinical Pharmacology and Therapeutics, 2026, 31(5): 691-699.
图 1 广藿香醇的分子平面立体结构[9];广藿香醇(C15H26O;相对分子质量:222)[10]
Fig.1 Two-dimensional and three-dimensional structural configurations of PA [9]; PA (C15H26O; molecular weight, 222)[10]
图 2 总结广藿香醇在抗炎、抗氧化应激、促进血管舒张三个机制中涉及到的主要的细胞因子及信号通路
Fig.2 Summary of the major cytokines and signaling pathways involved in PA's mechanisms of action, including anti-inflammatory, antioxidant stress, and vasodilation-promoting effects
| 作者 | 年份 | 动物 | 模型 | 干预 | 结果 |
| Wei et al.[ | 2018 | C57BL/6J以 及ob/ob小鼠 | 大脑中脑动脉栓塞模型(MCAO)达到局灶性脑缺血再灌注模型 | C57BL/6J小鼠,缺血1小时后拔出导丝以恢复血液循环; ob/ob小鼠及其同窝对照小鼠,缺血45 min后进行再灌注。 | 广藿香醇显著减少梗死体积,降低神经系统学评分,减轻血脑屏障功能障碍。 |
| Lu et al.[ | 2022 | C57BL/6J 小鼠 | 丝线结扎左冠状动脉前降支。缺血30 min后,释放滑动结进行再灌注损伤(MI/R模型) | 治疗组小鼠术前分别腹腔注射广藿香醇(10、20、40 mg/kg),持续30 d。 | 广藿香醇减少心肌细胞的凋亡,降低炎性细胞的浸润程度。 |
| Wu et al.[ | 2020 | Sprague-Dawley大鼠、BALB/C小鼠 | TNBS、DSS诱导的溃疡性结肠炎(UC)模型 | TNBS组:对照组和模型组大鼠给予10 mg/kg 广藿香醇; DSS组:从第14天到第27天,广藿香醇治疗组(15 mg/kg和30 mg/kg)的小鼠通过灌胃给予广藿香醇,而对照组和DSS组的小鼠在同一时间段内给予含2% Tween 80的溶液。 | 在两种模型中,广藿香醇显著降低促炎细胞因子的水平,并且维持肠道屏障的完整性,显著减轻结肠的组织学损伤,包括减少炎症细胞浸润等。 |
| Xu et al.[ | 2021 | Wistar大鼠 | 在不同时间点胃内给予65%的乙醇(10 mL/kg),建立急性肝损伤模型 | 试验组每日口服相应剂量的试验溶液,对照组和模型组口服相同剂量的Tween 80蒸馏水。 | 广藿香醇干预后表现出明显的肝损伤改善,抑制氧化应激反应,改善肠道屏障功能,减轻炎症反应,肠道微生物的多样性。 |
| Yu et al.[ | 2015 | BALB/C小鼠 | 鼻内灌注LPS以诱导 的急性肺损伤模型 | 实验组:给予小鼠一定剂量的广藿香醇进行预处理;对照组:未给予广藿香醇干预,或给予其他非相关药物作为对照,如右美托咪定(常用作急性肺损伤阳性对照药物)。 | 广藿香醇显著提高LPS诱导的急性肺损伤小鼠的生存率,减轻小鼠肺组织的病理损伤和肺水肿程度 |
| Li et al.[ | 2023 | SHRs大鼠、Wistar-Kyoto大鼠 | 自发性高血压建立肾纤维化模型 | 高、中、低广藿香醇剂量组分别给予不同剂量的广藿香醇(20、40、80 mg/kg,i.g.)。 Wistar-Kyoto大鼠为对照组,给予生理盐水(10 mL/kg, i.g.)。 | 广藿香醇显著降低自发性高血压大鼠的血压;减轻自发性高血压大鼠肾脏的纤维化程度,并且改善了自发性高血压大鼠的肾功能。 |
表 1 广藿香醇对缺血性疾病的主要治疗机制
Table 1 Primary therapeutic mechanisms of PA in ischemic diseases
| 作者 | 年份 | 动物 | 模型 | 干预 | 结果 |
| Wei et al.[ | 2018 | C57BL/6J以 及ob/ob小鼠 | 大脑中脑动脉栓塞模型(MCAO)达到局灶性脑缺血再灌注模型 | C57BL/6J小鼠,缺血1小时后拔出导丝以恢复血液循环; ob/ob小鼠及其同窝对照小鼠,缺血45 min后进行再灌注。 | 广藿香醇显著减少梗死体积,降低神经系统学评分,减轻血脑屏障功能障碍。 |
| Lu et al.[ | 2022 | C57BL/6J 小鼠 | 丝线结扎左冠状动脉前降支。缺血30 min后,释放滑动结进行再灌注损伤(MI/R模型) | 治疗组小鼠术前分别腹腔注射广藿香醇(10、20、40 mg/kg),持续30 d。 | 广藿香醇减少心肌细胞的凋亡,降低炎性细胞的浸润程度。 |
| Wu et al.[ | 2020 | Sprague-Dawley大鼠、BALB/C小鼠 | TNBS、DSS诱导的溃疡性结肠炎(UC)模型 | TNBS组:对照组和模型组大鼠给予10 mg/kg 广藿香醇; DSS组:从第14天到第27天,广藿香醇治疗组(15 mg/kg和30 mg/kg)的小鼠通过灌胃给予广藿香醇,而对照组和DSS组的小鼠在同一时间段内给予含2% Tween 80的溶液。 | 在两种模型中,广藿香醇显著降低促炎细胞因子的水平,并且维持肠道屏障的完整性,显著减轻结肠的组织学损伤,包括减少炎症细胞浸润等。 |
| Xu et al.[ | 2021 | Wistar大鼠 | 在不同时间点胃内给予65%的乙醇(10 mL/kg),建立急性肝损伤模型 | 试验组每日口服相应剂量的试验溶液,对照组和模型组口服相同剂量的Tween 80蒸馏水。 | 广藿香醇干预后表现出明显的肝损伤改善,抑制氧化应激反应,改善肠道屏障功能,减轻炎症反应,肠道微生物的多样性。 |
| Yu et al.[ | 2015 | BALB/C小鼠 | 鼻内灌注LPS以诱导 的急性肺损伤模型 | 实验组:给予小鼠一定剂量的广藿香醇进行预处理;对照组:未给予广藿香醇干预,或给予其他非相关药物作为对照,如右美托咪定(常用作急性肺损伤阳性对照药物)。 | 广藿香醇显著提高LPS诱导的急性肺损伤小鼠的生存率,减轻小鼠肺组织的病理损伤和肺水肿程度 |
| Li et al.[ | 2023 | SHRs大鼠、Wistar-Kyoto大鼠 | 自发性高血压建立肾纤维化模型 | 高、中、低广藿香醇剂量组分别给予不同剂量的广藿香醇(20、40、80 mg/kg,i.g.)。 Wistar-Kyoto大鼠为对照组,给予生理盐水(10 mL/kg, i.g.)。 | 广藿香醇显著降低自发性高血压大鼠的血压;减轻自发性高血压大鼠肾脏的纤维化程度,并且改善了自发性高血压大鼠的肾功能。 |
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