Cardiovascular protection of YiyiFuzi powder and the potential mechanisms through modulating mitochondria-endoplasmic reticulum interactions

被引:2
作者
Ding, Jingyi [1 ]
Ji, Ran [2 ]
Wang, Ziyi [1 ]
Jia, Yuzhi [1 ]
Meng, Tiantian [3 ]
Song, Xinbin [4 ]
Gao, Jing [1 ]
He, Qingyong [1 ]
机构
[1] China Acad Chinese Med Sci, Guanganmen Hosp, Dept Cardiol, Beijing, Peoples R China
[2] China Acad Chinese Med Sci, Guanganmen Hosp, Dept Intens Care Unit, Beijing, Peoples R China
[3] Beijing Univ Chinese Med, Dongfang Hosp, Dept Rehabil, Beijing, Peoples R China
[4] Henan Univ Chinese Med, Grad Sch, Zhengzhou, Peoples R China
关键词
cardiovascular disease; mitochondria; endoplasmic reticulum; Chinese herbal medicine; YiYiFuZi powder; UNFOLDED PROTEIN RESPONSE; LATERALIS RADIX PRAEPARATA; COIX SEED OIL; MA-YUEN-STAPF; ACONITI-LATERALIS; ER STRESS; SKELETAL-MUSCLE; HEART-FAILURE; ADLAY SEED; OXIDATIVE-PHOSPHORYLATION;
D O I
10.3389/fphar.2024.1405545
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Cardiovascular diseases (CVD) remain the leading cause of death worldwide and represent a major public health challenge. YiyiFuzi Powder (YYFZ), composed of Coicis semen and Fuzi, is a classical traditional Chinese medicine prescription from the Synopsis of Golden Chamber dating back to the Han Dynasty. Historically, YYFZ has been used to treat various CVD, rooted in Chinese therapeutic principles. Network pharmacology analysis indicated that YYFZ may exhibit direct or indirect effects on mitochondria-endoplasmic reticulum (ER) interactions. This review, focusing on the cardiovascular protective effects of Coicis semen and Fuzi, summarizes the potential mechanisms by which YYFZ acts on mitochondria and the ER. The underlying mechanisms are associated with regulating cardiovascular risk factors (such as blood lipids and glucose), impacting mitochondrial structure and function, modulating ER stress, inhibiting oxidative stress, suppressing inflammatory responses, regulating cellular apoptosis, and maintaining calcium ion balance. The involved pathways include, but were not limited to, upregulating the IGF-1/PI3K/AKT, cAMP/PKA, eNOS/NO/cGMP/SIRT1, SIRT1/PGC-1 alpha, Klotho/SIRT1, OXPHOS/ATP, PPAR alpha/PGC-1 alpha/SIRT3, AMPK/JNK, PTEN/PI3K/AKT, beta 2-AR/PI3K/AKT, and modified Q cycle signaling pathways. Meanwhile, the MCU, NF-kappa B, and JAK/STAT signaling pathways were downregulated. The PERK/eIF2 alpha/ATF4/CHOP, PERK/SREBP-1c/FAS, IRE1, PINK1-dependent mitophagy, and AMPK/mTOR signaling pathways were bidirectionally regulated. High-quality experimental studies are needed to further elucidate the underlying mechanisms of YYFZ in CVD treatment.
引用
收藏
页数:24
相关论文
共 255 条
  • [1] TGF-β1 stimulates mitochondrial oxidative phosphorylation and generation of reactive oxygen species in cultured mouse podocytes, mediated in part by the mTOR pathway
    Abe, Yoshifusa
    Sakairi, Toru
    Beeson, Craig
    Kopp, Jeffrey B.
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 2013, 305 (10) : F1477 - F1490
  • [2] PGC-1a Is a Master Regulator of Mitochondrial Lifecycle and ROS Stress Response
    Abu Shelbayeh, Othman
    Arroum, Tasnim
    Morris, Silke
    Busch, Karin B.
    [J]. ANTIOXIDANTS, 2023, 12 (05)
  • [3] Mitochondrial Oxidative Phosphorylation defect in the Heart of Subjects with Coronary Artery Disease
    Ait-Aissa, Karima
    Blaszak, Scott C.
    Beutner, Gisela
    Tsaih, Shirng-Wern
    Morgan, Garrett
    Santos, Janine H.
    Flister, Michael J.
    Joyce, David L.
    Camara, Amadou K. S.
    Gutterman, David D.
    Donato, Anthony J.
    Porter, George A., Jr.
    Beyer, Andreas M.
    [J]. SCIENTIFIC REPORTS, 2019, 9 (1)
  • [4] Alberts B, 2002, MOL BIOL CELL
  • [5] Protective Mechanisms of Mitochondria and Heart Function in Diabetes
    Aon, Miguel A.
    Tocchetti, Carlo G.
    Bhatt, Niraj
    Paolocci, Nazareno
    Cortassa, Sonia
    [J]. ANTIOXIDANTS & REDOX SIGNALING, 2015, 22 (17) : 1563 - 1586
  • [6] Chemical components and monoamine oxidase B inhibition activities from the tubers of Sauromatum giganteum (Engl.) Cusimano & Hett
    Ayeni, Emmanuel Ayodeji
    Ma, Chao
    Zhang, Yong-Mei
    Fan, Wen-Qin
    Liao, Xun
    [J]. NATURAL PRODUCT RESEARCH, 2023, 37 (17) : 2916 - 2923
  • [7] Opening of the mitochondrial permeability transition pore induces reactive oxygen species production at the level of the respiratory chain complex I
    Batandier, C
    Leverve, X
    Fontaine, E
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (17) : 17197 - 17204
  • [8] mTOR complex 2-Akt signaling at mitochondria-associated endoplasmic reticulum membranes (MAM) regulates mitochondrial physiology
    Betz, Charles
    Stracka, Daniele
    Prescianotto-Baschong, Cristina
    Frieden, Maud
    Demaurex, Nicolas
    Hall, Michael N.
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2013, 110 (31) : 12526 - 12534
  • [9] Mitochondrial superoxide: Production, biological effects, and activation of uncoupling proteins
    Brand, MD
    Affourtit, C
    Esteves, TC
    Green, K
    Lambert, AJ
    Miwa, S
    Pakay, JL
    Parker, N
    [J]. FREE RADICAL BIOLOGY AND MEDICINE, 2004, 37 (06) : 755 - 767
  • [10] Cao J, 2005, CHINESE MED J-PEKING, V118, P505