Ganoderma Lucidum Alleviates Ischemia-Reperfusion–induced Renal Injury in Wistar Rats

dc.contributor.author Dönder, A.
dc.contributor.author Aşır, F.
dc.date.accessioned 2022-05-13T06:54:14Z
dc.date.available 2022-05-13T06:54:14Z
dc.date.issued 2021
dc.description.abstract OBJECTIVE: To investigate effects of Ganoderma lucidum (G. lucidum) kidney sections of rats induced by ischemiareperfusion (I/R) injury. STUDY DESIGN: A total of 40 rats were assigned to 4 groups: control (Sham), I/R, G. lucidum, and I/R+G. lucidum groups. Prior to animal experiments, 20 mL/kg G. lucidum was administered to the G. lucidum–treated groups for 7 days. The control and I/R groups received only saline solution. The kidney was exposed to hypoxia for 1 hour by clamping renal vessels and was then allowed to reoxygenate for 6 hours. Blood was taken to measure for serum MDA, MPO, and GSH. Kidney tissues were resected for histological paraffin tissue protocol. Hematoxylineosin and immunohistochemical staining were performed. RESULTS: MDA and MPO levels were highest in the I/R group but were close to the levels of the control group in the I/R+G. lucidum group. Unlike MDA and MPO values, GSH values were the lowest in the I/R group, but after G. lucidum treatment, GSH levels increased in the I/R+G. lucidum group. In kidney sections of hematoxylineosin staining, the control group showed no pathology. In the I/R group, atrophic glomeruli, degenerated tubular cells, and mononuclear cell infiltration with dilated and congested vessels were observed. In the I/R+G. lucidum group, I/R pathology was mostly recovered. In the G. lucidum group, ADAMTS4 expression was moderately expressed in glomerular and tubular cells. The I/R group showed positive ADAMTS4 expression in mostly inflammatory cells. In the I/R+G. lucidum group, ADAMTS4 was positively expressed only in glomerular structures. In the G. lucidum group, caspase3 expression was observed in glomerular and tubular cells. The I/R group showed strong caspase3 activity in glomerular and tubular cells, in vascular cells, and inflammatory cells. The I/R+G. lucidum group showed weak caspase3 expression. CONCLUSION: Ischemiareperfusion injury caused histopathological and biochemical alterations in renal tissue; G. lucidum protected tissue structure and integrity by its antioxidant and antiinflammatory properties. © Science Printers and Publishers, Inc. en_US
dc.identifier.citation Dönder, A. ve Aşır, F. (2021). Ganoderma lucidum alleviates ischemia- reperfusion-induced renal injury in wistar rats. Analytical and Quantitave Cytopathology and Histopathology, 43(5), 484-492. en_US
dc.identifier.issn 2578-742X
dc.identifier.scopus 2-s2.0-85129255699
dc.indekslendigikaynak Web of Science en_US
dc.indekslendigikaynak Scopus en_US
dc.language.iso en en_US
dc.publisher Science Printers and Publishers Inc. en_US
dc.relation.ispartof Analytical and Quantitative Cytopathology and Histopathology en_US
dc.rights info:eu-repo/semantics/closedAccess en_US
dc.subject Chinese Herbal Drugs en_US
dc.subject Chinese Traditional Medicine en_US
dc.subject Ganoderma Lucidum en_US
dc.subject Ischemia-Reperfusion Injury en_US
dc.subject Renal Ischemia-Reperfusion en_US
dc.title Ganoderma Lucidum Alleviates Ischemia-Reperfusion–induced Renal Injury in Wistar Rats en_US
dc.type Article en_US
dspace.entity.type Publication
gdc.author.scopusid 57189211476
gdc.author.scopusid 57347745200
gdc.coar.access metadata only access
gdc.coar.type text::journal::journal article
gdc.description.department Artuklu University en_US
gdc.description.departmenttemp [Dönder A.] Vocational School of Health Services, Mardin Artuklu University; [Aşır F.] Department of Histology and Embryology, Medical School, Dicle University en_US
gdc.description.endpage 492 en_US
gdc.description.issue 5 en_US
gdc.description.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
gdc.description.scopusquality N/A
gdc.description.startpage 484 en_US
gdc.description.volume 43 en_US
gdc.description.wosquality N/A
gdc.identifier.wos WOS:000765842800001
gdc.scopus.citedcount 0
gdc.wos.citedcount 0

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