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Published:
Mar 24, 2026DOI:
10.4314/tjpr.v25i2.8Keywords:
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Azma Rosida, Department of Clinical Pathology, Faculty of Medicine and Health Science, Universitas Lambung Mangkurat, Banjarbaru, Indonesia.
Nia Kania, Department of Anatomic Pathology, Faculty of Medicine and Health Science, Universitas Lambung Mangkurat, Banjarbaru, Indonesia.
Fujiati, Biochemistry Laboratory, Faculty of Medicine and Health Science, Universitas Lambung Mangkurat, Banjarbaru, Indonesia.
Triawanti, Biochemistry Laboratory, Faculty of Medicine and Health Science, Universitas Lambung Mangkurat, Banjarbaru, Indonesia.
Ika Oktaviyanti, Department of Anatomic Pathology, Faculty of Medicine and Health Science, Universitas Lambung Mangkurat, Banjarbaru, Indonesia.
Roselina Panghiyangani, Biology Laboratory, Faculty of Medicine and Health Science, Universitas Lambung Mangkurat, Banjarbaru, Indonesia.
Nur Arfian, Department of Anatomy, Faculty of Medicine, Public Health and Nursing, Universitas Gajah Mada, Sleman, Indonesia.
Main Article Content
Garcinia forbesii King leaf extract protects against renal tubular injury in ischemia- reperfusion injury via IL-18 and oxidative stress reduction
Azma Rosida
Nia Kania
Mohammad Rudiansyah
Fujiati
Triawanti
Ika Oktaviyanti
Roselina Panghiyangani
Nur Arfian
Abstract
Purpose: To evaluate the protective effects of Garcinia forbesii King leaf extract against renal tubular injury induced by Renal ischemia–reperfusion injury (IRI) and to assess its association with inflammatory and oxidative stress markers, including interleukin-18 (IL-18), superoxide dismutase 2 (SOD2), and malondialdehyde (MDA).
Methods: Male Wistar rats were subjected to renal IRI and treated with Garcinia forbesii King leaf extract at doses of 2.5, 25, and 250 mg/kg. Renal IL-18 levels, SOD2 expression, serum MDA levels, and histopathological tubular injury scores were evaluated.
Results: Renal IL-18 levels were significantly increased in IRI group compared with the sham-operated group. Treatment with Garcinia forbesii King leaf extract at doses of 25 and 250 mg/kg significantly reduced renal IL-18 levels. The medium dose (25 mg/kg) significantly increased renal SOD2 expression and reduced serum MDA levels. Histopathological analysis showed that low- and medium-dose treatments attenuated renal tubular injury, whereas the high dose did not provide additional histological protection.
Conclusion: Garcinia forbesii King leaf extract exerts nephroprotective effects against IRI-induced renal injury, likely through modulation of inflammatory responses and oxidative stress.


