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dc.contributor.authorWihastuti, Titin Andri
dc.contributor.authorAini, Fitria Nugraha
dc.contributor.authorTjahjono, Cholid Tri
dc.contributor.authorSulfia, Yuni Hendrati
dc.contributor.authorSholichah, Zuhrotus
dc.contributor.authorHeriansyah, Teuku
dc.date.accessioned2021-10-14T01:43:25Z
dc.date.available2021-10-14T01:43:25Z
dc.date.issued2019-11-01
dc.identifier.issn503–508
dc.identifier.urihttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6830380/
dc.identifier.urihttp://repository.unisma.ac.id/handle/123456789/2032
dc.description[ARCHIVES] Copyright Article from: Vascular Health and Risk Management (US National Library of Medicine National Institutes of Health)en_US
dc.description.abstractPurpose The aim of this study is to prove that type 2 diabetes mellitus can induce increasing inflammation marker in renal and that the provision of darapladib as Lp-LA2 Inhibitor agents can inhibit inflammation that were measured from the expression of IL-1B and IL-6- type cytokine in renal. This study also discusses the correlation between IL-1B and IL-6- type cytokine expression in renal. Methods Thirty Sprague-Dawley (SD) rats were divided into three main groups; those are negative control group (NC), Type 2 Diabetes Mellitus group (T2DM) given high fat diet (HFD) with streptozotocin intraperitoneal injection (35mg/kg BW) and diabetes mellitus + darapladib group (DM + DP). Each group was treated within two serial treatment time: 8 weeks and 16 weeks. Expressions of IL-1B and IL-6- type cytokine in renal were the markers that we measured by immunofluorosense method. Results The administration of darapladib can significantly decrease the expression of IL-1B- type cytokine (p ANOVA = 0.029, p < 0.005) measured in rats’ renal both at weeks 8 and 16 in the T2DM group. The Expression of IL-6- type cytokine also showed a significant difference after treated with darapladib both at weeks 8 and 16 in T2DM group with p-value of ANOVA = 0.033, p < 0.005. The Pearson correlation showed a strong correlation (linear regression value was r2 = 0.743). Conclusion Our results show that atherosclerosis caused by inflammation in renal T2DM SD rats could be inhibited by the administration of darapladib.en_US
dc.language.isoenen_US
dc.publisherUS National Library of Medicine National Institutes of Healthen_US
dc.relation.ispartofseriesVascular Health and Risk Management;
dc.subjectIL-1B- type cytokineen_US
dc.subjectIL-6- type cytokineen_US
dc.subjectkidney organen_US
dc.subjectdiabetes mellitus type 2en_US
dc.subjectdarapladiben_US
dc.titleLp-PLA2 Selective Inhibitor (Darapladib) Effect In Lowering The Expression Level Of IL-1B And IL-6 In The Renal At Type 2 Diabetes Mellitusen_US
dc.typeArticleen_US


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