[1] SATIN L S, SOLEIMANPOUR S A, WALKER E M. New aspects of diabetes research and therapeutic development[J]. Pharmacol Rev, 2021, 73(3):1001-1015. doi:  10.1124/pharmrev.120.000160
[2] HUANG X Y, CHU Y, REN H, et al. Antioxidation function of EGCG by activating Nrf2/HO-1 pathway in mice with coronary heart disease[J]. Contrast Med Mol Imaging, 2022, 2022:1-8.
[3] SUN H, SAEEDI P, KARURANGA S, et al. IDF Diabetes Atlas: Global, regional and country-level diabetes prevalence estimates for 2021 and projections for 2045[J]. Diabetes Res Clin Pract, 2022, 183:109119. doi:  10.1016/j.diabres.2021.109119
[4] TIAN X, GAO Y, ZHONG M, et al. The association between serum Sestrin2 and the risk of coronary heart disease in patients with type 2 diabetes mellitus[J]. BMC Cardiovas Disord, 2022, 22(1):1-8. doi:  10.1186/s12872-021-02434-3
[5] CAI X L, SHEN J, YE B Q, et al. Characteristics, treatment patterns, and glycemic control of older type 2 diabetes mellitus patients in China[J]. Chin Med J, 2021, 134(23):2893-2895. doi:  10.1097/CM9.0000000000001674
[6] KATSIKI N, BANACH M, MIKHAILIDIS D P. Is type 2 diabetes mellitus a coronary heart disease equivalent or not? Do not just enjoy the debate and forget the patient![J]. Arch Med Sci, 2019, 15(6):1357-1364. doi:  10.5114/aoms.2019.89449
[7] 钟钰灵. 基于网络药理学的麝香保心丸治疗冠状动脉微循环疾病的机制研究[D]. 桂林: 桂林医学院, 2022.
[8] 叶健, 李凌燕, 席鑫, 等. 麝香保心丸基于miR-144-3p/SLC7A11通路减轻心肌细胞铁死亡的机制研究[J]. 中国中西医结合杂志, 2022, 42(11):1335-1340.
[9] 李芃琪, 信琪琪, 袁蓉, 等. 麝香保心丸调控冠心病血管新生的研究进展[J]. 中国实验方剂学杂志, 2022, 28(14):242-253.
[10] 侯志杰. 麝香保心丸治疗冠心病合并2型糖尿病患者55例临床观察[J]. 医学理论与实践, 2014, 27(20):2701-2702.
[11] 费震宇, 徐玫, 陈宇明, 等. 麝香保心丸对2型糖尿病患者尿微量白蛋白/肌酐比值的影响[J]. 上海医药, 2020, 41(10):23-25.
[12] 李勇萍, 杜从云, 刘桃喜. 麝香保心丸对冠心病伴糖尿病患者发生心血管临床事件的影响分析[J]. 中西医结合心血管病电子杂志, 2018, 6(18): 163, 166.
[13] 华姞安, 孟靓, 孟智睿, 等. 中成药治疗2型糖尿病用药规律及作用靶点分析[J]. 世界中医药, 2023, 18(5):692-698,703. doi:  10.3969/j.issn.1673-7202.2023.05.019
[14] 卢李娜, 郑娴. 从气虚血瘀论治冠心病的研究进展[J]. 实用中医内科杂志, 2023, 37(4):38-41.
[15] 中国医师协会中西医结合医师分会心血管病专业委员会, 国家中医心血管病临床医学研究中心. 麝香保心丸治疗冠心病专家共识[J]. 中国中西医结合杂志, 2022, 42(7):782-790.
[16] 李桂梅, 谢秀峰. 麝香保心丸配合强化抗血小板治疗对急性心肌梗死合并糖尿病患者疗效研究[J]. 创伤与急危重病医学, 2020, 8(6):426-430.
[17] 郭施勉, 楚英杰. 人参皂苷Rg1对冠心病大鼠心肌细胞凋亡的影响及机制研究[J]. 中西医结合心脑血管病杂志, 2021, 19(23):4054-4059. doi:  10.12102/j.issn.1672-1349.2021.23.008
[18] ZHOU P, XIE W J, HE S B, et al. Ginsenoside Rb1 as an anti-diabetic agent and its underlying mechanism analysis[J]. Cells, 2019, 8(3):204. doi:  10.3390/cells8030204
[19] FAN X, ZHANG C, NIU S, et al. Ginsenoside Rg1 attenuates hepatic insulin resistance induced by high-fat and high-sugar by inhibiting inflammation[J]. Eur J Pharmacol, 2019, 854:247-255. doi:  10.1016/j.ejphar.2019.04.027
[20] CHANG X, ZHANG T, ZHANG W, et al. Natural drugs as a treatment strategy for cardiovascular disease through the regulation of oxidative stress[J]. Oxidative Med Cell Longevity, 2020, 2020:5430407.
[21] LI W, QIAO J, LIN K, et al. Ethyl-acetate fraction from a cinnamon-cortex extract protects pancreatic β-cells from oxidative stress damage[J]. Front Pharmacol, 2023, 14:1111860. doi:  10.3389/fphar.2023.1111860
[22] NAIR A, PREETHA RANI M R, SALIN RAJ P, et al. Cinnamic acid is beneficial to diabetic cardiomyopathy via its cardioprotective, anti-inflammatory, anti-dyslipidemia, and antidiabetic properties[J]. J Biochemi Molecular Toxicol, 2022, 36(12):e23215. doi:  10.1002/jbt.23215
[23] 王笑, 张恒, 李媛媛, 等. 肉桂醛预处理对H9C2心肌细胞缺氧复氧损伤后自噬的影响[J]. 中药药理与临床, 2021, 37(3):30-34.
[24] 赵丹, 王明慧, 张程斐, 等. 肉桂酸对db/db小鼠肝脏PI3K/AKT/FoxO1信号通路的影响[J]. 世界科学技术(中医药现代化), 2021, 23(10):3613-3620.
[25] CHEN Y S, LIU H M, LEE T Y. Ursodeoxycholic acid regulates hepatic energy homeostasis and white adipose tissue macrophages polarization in leptin-deficiency obese mice [J]. Cells, 2019, 8(3):253.
[26] LI D D, ZHONG J X, ZHANG Q R, et al. Effects of anti-inflammatory therapies on glycemic control in type 2 diabetes mellitus[J]. Front Immunol, 2023, 14:1125116. doi:  10.3389/fimmu.2023.1125116
[27] AKBARI M, HASSAN-ZADEH V. IL-6 signalling pathways and the development of type 2 diabetes[J]. Inflammopharmacol, 2018, 26(3):685-698. doi:  10.1007/s10787-018-0458-0
[28] RIDKER P M, RANE M. Interleukin-6 signaling and anti-interleukin-6 therapeutics in cardiovascular disease[J]. Circ Res, 2021, 128(11):1728-1746. doi:  10.1161/CIRCRESAHA.121.319077
[29] WAGNER N, WAGNER K D. Pharmacological utility of PPAR modulation for angiogenesis in cardiovascular disease[J]. Int Mol Sci, 2023, 24(3):2345. doi:  10.3390/ijms24032345
[30] JIN J L, ZHU C, WANG J X, et al. The association between ACTB methylation in peripheral blood and coronary heart disease in a case-control study[J]. Front Cardiovasc Med, 2022, 9:972566. doi:  10.3389/fcvm.2022.972566
[31] BOUTCHUENG-DJIDJOU M, BELLEAU P, BILODEAU N, et al. A type 2 diabetes disease module with a high collective influence for Cdk2 and PTPLAD1 is localized in endosomes[J]. PLoS One, 2018, 13(10):e0205180. doi:  10.1371/journal.pone.0205180
[32] WAGHELA B N, VAIDYA F U, RANJAN K, et al. AGE-RAGE synergy influences programmed cell death signaling to promote cancer[J]. Mol Cell Biochem, 2021, 476(2):585-598. doi:  10.1007/s11010-020-03928-y
[33] SHEN C Y, LU C H, WU C H, et al. The development of Maillard reaction, and advanced glycation end product (AGE)-receptor for AGE (RAGE) signaling inhibitors as novel therapeutic strategies for patients with AGE-related diseases[J]. Mol, 2020, 25(23):5591. doi:  10.3390/molecules25235591
[34] KOSMOPOULOS M, DREKOLIAS D, ZAVRAS P D, et al. Impact of advanced glycation end products (AGEs) signaling in coronary artery disease[J]. Biochim Biophys Acta BBA Mol Basis Dis, 2019, 1865(3):611-619. doi:  10.1016/j.bbadis.2019.01.006
[35] BRENNAN J J, GILMORE T D. Evolutionary origins of toll-like receptor signaling[J]. Mol Biol Evol, 2018, 35(7):1576-1587. doi:  10.1093/molbev/msy050
[36] KOUSHKI K, SHAHBAZ S K, MASHAYEKHI K, et al. Anti-inflammatory action of statins in cardiovascular disease: the role of inflammasome and toll-like receptor pathways[J]. Clinic Rev Allerg Immunol, 2021, 60(2):175-199. doi:  10.1007/s12016-020-08791-9
[37] AAMIR K, KHAN H U, SETHI G, et al. Wnt signaling mediates TLR pathway and promote unrestrained adipogenesis and metaflammation: therapeutic targets for obesity and type 2 diabetes[J]. Pharmacol Res, 2020, 152:104602. doi:  10.1016/j.phrs.2019.104602
[38] ZACCOLO M, ZERIO A, LOBO M J. Subcellular organization of the cAMP signaling pathway[J]. Pharmacol Rev, 2021, 73(1):278-309. doi:  10.1124/pharmrev.120.000086
[39] WANG Y N, LIU Q, KANG S G, et al. Dietary bioactive ingredients modulating the cAMP signaling in diabetes treatment[J]. Nutrients, 2021, 13(9):3038. doi:  10.3390/nu13093038
[40] SADEK M S, CACHORRO E, EL-ARMOUCHE A, et al. Therapeutic implications for PDE2 and cGMP/cAMP mediated crosstalk in cardiovascular diseases[J]. Int J Mol Sci, 2020, 21(20):7462.
[41] 张晓囡, 孙长鑫, 陈纪烨, 等. 基于“异病同治”理论探讨四妙勇安汤在心血管疾病中的应用[J]. 中西医结合心脑血管病杂志, 2023, 21(5):946-949. doi:  10.12102/j.issn.1672-1349.2023.05.040