Publikasi Scopus 2025 per tanggal 31 Januari 2025 (67 artikel)

Ilyas S.; Midoen Y.H.; Santoso P.
Ilyas, Syafruddin (55980597400); Midoen, Yurnadi Hanafi (57197805109); Santoso, Putra (56082215500)
55980597400; 57197805109; 56082215500
A novel therapeutic approach to doxorubicin-induced cardiotoxicity, with a particular emphasis on the potential cardioprotective properties of Vitis gracilis Wall.; [Un nuevo enfoque terapéutico para la cardiotoxicidad inducida por doxorrubicina, con especial énfasis en las posibles propiedades cardioprotectoras de Vitis gracilis Wall.]
2025
Journal of Pharmacy and Pharmacognosy Research
13
1
254
263
9
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Study Program of Biology, Faculty of Mathematics and Natural Sciences, Universitas Sumatera Utara, Medan, Indonesia; Department of Medical Biology, Faculty of Medicine, Universitas Indonesia, Jakarta, Indonesia; Department of Biology, Faculty of Mathematics and Natural Sciences, Universitas Andalas, Padang, Indonesia
Ilyas S., Study Program of Biology, Faculty of Mathematics and Natural Sciences, Universitas Sumatera Utara, Medan, Indonesia; Midoen Y.H., Department of Medical Biology, Faculty of Medicine, Universitas Indonesia, Jakarta, Indonesia; Santoso P., Department of Biology, Faculty of Mathematics and Natural Sciences, Universitas Andalas, Padang, Indonesia
Context: Doxorubicin, a potent chemotherapy drug, often leads to cardiotoxicity, limiting its clinical use. This study investigates the potential of Vitis gracilis Wall. nanoherbs (VGN) in mitigating doxorubicin-induced heart damage, aiming to provide insights into its therapeutic efficacy as a cardioprotective agent. Aims: To evaluate the therapeutic potential of VGN in mitigating doxorubicin-induced cardiotoxicity. Methods: The study comprised four treatment groups in male Wistar rats: D0 (negative control), D+ (doxorubicin 0.00038 mg/200 g body weight (BW)/day), DC (doxorubicin + Vitamin C 0.04 mg/200 g BW/d), D25 (doxorubicin + VGN at 25 mg/200 g BW/d), and D30 (doxorubicin + VGN at 30 mg/200 g BW/d). Key cardiac parameters, including LDH, CK-MB, TNF-alpha, IL-10, SOD, and caspase 3, were meticulously measured to assess cardioprotective effects. Statistical analyses were performed to evaluate the significance of observed changes, revealing a dose-dependent reduction in markers of cardiac injury (LDH, CK-MB) and inflammation (TNF-alpha) alongside enhancements in antioxidant defenses (SOD) and inhibition of apoptosis (caspase 3) with VGN administration. Results: The results showed promising reductions in markers of heart injury (LDH, CK-MB) and inflammation (TNF-alpha) specifically at a dose of 30 mg/200 g BW/d significantly (p<0.05). In addition, doses of 30 mg/200 g BW/d of VGN showed potential to increase antioxidant defenses (SOD), IL-10, as well as inhibit apoptosis (caspase 3) (p<0.05), highlighting the best multifaceted cardioprotective effects. Conclusions: The study demonstrates that V. gracilis has the potential to reduce doxorubicin-induced cardiotoxicity through its multifaceted cardioprotective effects. These effects include a reduction in markers of cardiac injury and inflammation at a dose of 30 mg/200 g BW/d, enhancement of antioxidant defenses, and inhibition of apoptosis. © 2025 Academic Association of Pharmaceutical Sciences from Antofagasta (ASOCIFA). All rights reserved.
cardiac parameters; cardiotoxicity mitigation; Vitis gracilis
antioxidant; apoptosis inhibitor; ascorbic acid; cardiac agent; caspase 3; creatine kinase MB; doxorubicin; interleukin 10; lactate dehydrogenase; plant extract; protective agent; superoxide dismutase; tumor necrosis factor; unclassified drug; Vitis gracilis extract; animal experiment; animal model; animal tissue; antiapoptotic activity; antioxidant activity; apoptosis; Article; cardiotoxicity; controlled study; dose response; drug efficacy; enzyme linked immunosorbent assay; heart injury; heart protection; male; nonhuman; rat
USU: Research of Talenta, Universitas Sumatera Utara
Authors thank USU: Research of Talenta, Universitas Sumatera Utara, Indonesian Collaborative Research Program (RKI), Scheme A, Fiscal Year 2023; Number: 237 1/UN5.2.3.1/PPM/KP-RKI/2023; UI: Indonesian Collaborative Research Program Assignment Agreement 16 PTHBH years 2023. Number: NKB-1065/UN2.RST/HKP.05.00/2023 Universitas Indonesia (UI); and UNAND: Indonesian Collaborative Research Grant for pro
Academic Association of Pharmaceutical Sciences from Antofagasta (ASOCIFA)
07194250
Article
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291
15992