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emodin and Cardiotoxicity

emodin has been researched along with Cardiotoxicity in 4 studies

Emodin: Purgative anthraquinone found in several plants, especially RHAMNUS PURSHIANA. It was formerly used as a laxative, but is now used mainly as a tool in toxicity studies.
emodin : A trihydroxyanthraquinone that is 9,10-anthraquinone which is substituted by hydroxy groups at positions 1, 3, and 8 and by a methyl group at position 6. It is present in the roots and barks of numerous plants (particularly rhubarb and buckthorn), moulds, and lichens. It is an active ingredient of various Chinese herbs.

Cardiotoxicity: Damage to the HEART or its function secondary to exposure to toxic substances such as drugs used in CHEMOTHERAPY; IMMUNOTHERAPY; or RADIATION.

Research Excerpts

ExcerptRelevanceReference
"Aloe-emodin (AE), a novel ferroptosis inhibitor, alleviates the doxorubicin (DOX)-induced cardiotoxicity in H9c2 rat cardiomyocytes."8.31Aloe-emodin alleviates doxorubicin-induced cardiotoxicity via inhibition of ferroptosis. ( Cai, W; Fang, J; He, Y; Xi, J; Zhang, B, 2023)
"Emodin has the potential to attenuate DIC by directly binding to GSDMD to inhibit pyroptosis."5.91Emodin attenuates cardiomyocyte pyroptosis in doxorubicin-induced cardiotoxicity by directly binding to GSDMD. ( Chen, Y; Dai, S; Fan, X; Han, J; Huang, W; Huang, Z; Lin, J; Liu, Q; Su, L; Ye, B; Zhang, Y; Zhong, L, 2023)
"Aloe-emodin (AE), a novel ferroptosis inhibitor, alleviates the doxorubicin (DOX)-induced cardiotoxicity in H9c2 rat cardiomyocytes."4.31Aloe-emodin alleviates doxorubicin-induced cardiotoxicity via inhibition of ferroptosis. ( Cai, W; Fang, J; He, Y; Xi, J; Zhang, B, 2023)
"Emodin has the potential to attenuate DIC by directly binding to GSDMD to inhibit pyroptosis."1.91Emodin attenuates cardiomyocyte pyroptosis in doxorubicin-induced cardiotoxicity by directly binding to GSDMD. ( Chen, Y; Dai, S; Fan, X; Han, J; Huang, W; Huang, Z; Lin, J; Liu, Q; Su, L; Ye, B; Zhang, Y; Zhong, L, 2023)

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's1 (25.00)24.3611
2020's3 (75.00)2.80

Authors

AuthorsStudies
He, Y1
Xi, J1
Fang, J1
Zhang, B1
Cai, W1
Dai, S1
Chen, Y1
Fan, X1
Han, J1
Zhong, L1
Zhang, Y1
Liu, Q1
Lin, J1
Huang, W1
Su, L1
Huang, Z1
Ye, B1
Birari, L1
Wagh, S1
Patil, KR1
Mahajan, UB1
Unger, B1
Belemkar, S1
Goyal, SN1
Ojha, S1
Patil, CR1
Esmat, AY1
Said, MM1
Khalil, SA1

Other Studies

4 other studies available for emodin and Cardiotoxicity

ArticleYear
Aloe-emodin alleviates doxorubicin-induced cardiotoxicity via inhibition of ferroptosis.
    Free radical biology & medicine, 2023, Volume: 206

    Topics: Aloe; Animals; Cardiotoxicity; Cell Line; Doxorubicin; Emodin; Ferroptosis; Myocytes, Cardiac; NF-E2

2023
Emodin attenuates cardiomyocyte pyroptosis in doxorubicin-induced cardiotoxicity by directly binding to GSDMD.
    Phytomedicine : international journal of phytotherapy and phytopharmacology, 2023, Volume: 121

    Topics: Animals; Cardiotoxicity; Doxorubicin; Emodin; Mice; Myocytes, Cardiac; Pyroptosis

2023
Aloin alleviates doxorubicin-induced cardiotoxicity in rats by abrogating oxidative stress and pro-inflammatory cytokines.
    Cancer chemotherapy and pharmacology, 2020, Volume: 86, Issue:3

    Topics: Animals; Antibiotics, Antineoplastic; Cardiotoxicity; Cathartics; Cytokines; Doxorubicin; Emodin; In

2020
Aloin: a natural antitumor anthraquinone glycoside with iron chelating and non-atherogenic activities.
    Pharmaceutical biology, 2015, Volume: 53, Issue:1

    Topics: Animals; Antineoplastic Agents, Phytogenic; Cardiotoxicity; Doxorubicin; Emodin; Glycosides; Heart;

2015