Page last updated: 2024-10-20

thiamine and Cardiotoxicity

thiamine has been researched along with Cardiotoxicity in 3 studies

thiamine(1+) : A primary alcohol that is 1,3-thiazol-3-ium substituted by (4-amino-2-methylpyrimidin-5-yl)methyl, methyl and 2-hydroxyethyl groups at positions 3, 4 and 5, respectively.

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
"To investigate the effect of thiamine and thiamine pyrophosphate on doxorubicin-induced cardiotoxicity biochemically and histopathologically and to examine whether doxorubicin cardiotoxicity is related to the conversion of thiamine into thiamine pyrophosphate and inhibition of thiamine pyrophosphokinase (TPK) enzyme."7.81Examination of the effects of thiamine and thiamine pyrophosphate on Doxorubicin-induced experimental cardiotoxicity. ( Akcay, F; Polat, B; Sener, E; Suleyman, H, 2015)
"This study investigated the effect of thiamine pyrophosphate on oxidative damage associated with cardiotoxicity caused by cisplatin (CIS), an antineoplastic agent, in rats, and compared this with thiamine."7.80The protective effect of thiamine pyrophosphate, but not thiamine, against cardiotoxicity induced with cisplatin in rats. ( Coskun, R; Gulapoglu, M; Turan, IS; Turan, MI, 2014)
"To investigate the effect of thiamine and thiamine pyrophosphate on doxorubicin-induced cardiotoxicity biochemically and histopathologically and to examine whether doxorubicin cardiotoxicity is related to the conversion of thiamine into thiamine pyrophosphate and inhibition of thiamine pyrophosphokinase (TPK) enzyme."3.81Examination of the effects of thiamine and thiamine pyrophosphate on Doxorubicin-induced experimental cardiotoxicity. ( Akcay, F; Polat, B; Sener, E; Suleyman, H, 2015)
"This study investigated the effect of thiamine pyrophosphate on oxidative damage associated with cardiotoxicity caused by cisplatin (CIS), an antineoplastic agent, in rats, and compared this with thiamine."3.80The protective effect of thiamine pyrophosphate, but not thiamine, against cardiotoxicity induced with cisplatin in rats. ( Coskun, R; Gulapoglu, M; Turan, IS; Turan, MI, 2014)

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's2 (66.67)24.3611
2020's1 (33.33)2.80

Authors

AuthorsStudies
Radonjic, T1
Rankovic, M1
Ravic, M1
Zivkovic, V1
Srejovic, I1
Jeremic, J1
Jeremic, N1
Sretenovic, J1
Matic, S1
Jakovljevic, V1
Nikolic Turnic, T1
Coskun, R1
Turan, MI1
Turan, IS1
Gulapoglu, M1
Polat, B1
Suleyman, H1
Sener, E1
Akcay, F1

Other Studies

3 other studies available for thiamine and Cardiotoxicity

ArticleYear
The Effects of Thiamine Hydrochloride on Cardiac Function, Redox Status and Morphometric Alterations in Doxorubicin-Treated Rats.
    Cardiovascular toxicology, 2020, Volume: 20, Issue:2

    Topics: Animals; Antioxidants; Cardiotoxicity; Coronary Circulation; Disease Models, Animal; Doxorubicin; Fe

2020
The protective effect of thiamine pyrophosphate, but not thiamine, against cardiotoxicity induced with cisplatin in rats.
    Drug and chemical toxicology, 2014, Volume: 37, Issue:3

    Topics: Animals; Antineoplastic Agents; Cardiotoxicity; Cisplatin; DNA Damage; Glutathione; Injections, Intr

2014
Examination of the effects of thiamine and thiamine pyrophosphate on Doxorubicin-induced experimental cardiotoxicity.
    Journal of cardiovascular pharmacology and therapeutics, 2015, Volume: 20, Issue:2

    Topics: Animals; Antibiotics, Antineoplastic; Cardiotoxicity; DNA Damage; Doxorubicin; Glutathione; Male; Ma

2015