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<title>Saudi Pharmaceutical Journal Agustus 2023</title>
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<place><placeTerm type="text">Arab Saudi</placeTerm></place>
<publisher>University of Jeddah</publisher>
<dateIssued>2023</dateIssued>
<issuance>monographic</issuance>
<edition>Agustus 2023</edition>
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<languageTerm type="text">Indonesia</languageTerm>
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<note>abstract

Previous investigations have shown that D. viscosa herbal extract is often used to treat a variety of dis-
eases. Therefore, the purpose of this study was to investigate any additional potential impacts on rat liver

and kidney damage induced by diabetes. Streptozotocin (STZ) (60 mg/kg/day) was given as a single
dosage to cause type 1 diabetes. After then, diabetic rats received oral doses of D. viscosa for four weeks
at 150 and 300 mg/kg/day. Blood, liver, and kidney tissues were collected at the end of the treatment and

examined. Analysis was made of the serum lipid profile, liver, and kidney functions, as well as blood bio-
chemistry. Moreover, the levels of tumor necrosis factor-alpha (TNF-a), interleukin-6 (IL-6), interleukin-1

beta (IL-1b), prostaglandin E-2 (PGE-2), and nitric oxide (NO) were estimated in serum. In liver and kid-
ney samples, thiobarbituric acid reactive substances (TBARs) and reduced glutathione (GSH), as well as

the pro-inflammatory cytokines and enzymatic activities of glutathione peroxidase (GPx), glutathione
reeducates (GR), glutathione-S-transferase (GST), catalase (CAT), and superoxide dismutase (SOD) were
analyzed. Histological changes in liver and kidney cross-sections were also observed. Our findings
demonstrated that D. viscosa dramatically decreased pro-inflammatory indicators in blood, kidney, and

liver tissues as well as blood glucose, and restored insulin levels, and lipid profiles. Additionally, it signif-
icantly raises the antioxidant enzyme activity SOD, CAT, GPx, and GST, while significantly lowering TBARs

levels. The above-mentioned biochemical changes that took place in tissues were further supported by
histological alterations. These findings imply that D. viscosa protects against STZ-induced hyperglycemia,
aberrant lipid synthesis, and oxidative stress and that these benefits may be mediated by interacting with
various targets to increase the levels of antioxidant enzymes in the liver and kidneys. Its mode of action
and safety for use as medicine against various metabolic problems caused by diabetes require more research.</note>
<subject authority=""><topic>Streptozotocin</topic></subject>
<subject authority=""><topic>Diabetes</topic></subject>
<subject authority=""><topic>Dodonaea viscosa</topic></subject>
<subject authority=""><topic>Oxidative stress</topic></subject>
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<physicalLocation>PERPUSTAKAAN SEKOLAH TINGGI ILMU KESEHATAN SAMARINDA REPOSITORY</physicalLocation>
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<sublocation>Perpus.Akfarsam (Jurnal Farmasi Internasional)</sublocation>
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