dc.contributor.author | Wihastuti, Titin Andri | |
dc.contributor.author | Aini, Fitria Nugraha | |
dc.contributor.author | Tjahjono, Cholid Tri | |
dc.contributor.author | Sulfia, Yuni Hendrati | |
dc.contributor.author | Sholichah, Zuhrotus | |
dc.contributor.author | Heriansyah, Teuku | |
dc.date.accessioned | 2021-10-14T01:43:25Z | |
dc.date.available | 2021-10-14T01:43:25Z | |
dc.date.issued | 2019-11-01 | |
dc.identifier.issn | 503–508 | |
dc.identifier.uri | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6830380/ | |
dc.identifier.uri | http://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.abstract | Purpose
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.iso | en | en_US |
dc.publisher | US National Library of Medicine National Institutes of Health | en_US |
dc.relation.ispartofseries | Vascular Health and Risk Management; | |
dc.subject | IL-1B- type cytokine | en_US |
dc.subject | IL-6- type cytokine | en_US |
dc.subject | kidney organ | en_US |
dc.subject | diabetes mellitus type 2 | en_US |
dc.subject | darapladib | en_US |
dc.title | Lp-PLA2 Selective Inhibitor (Darapladib) Effect In Lowering The Expression Level Of IL-1B And IL-6 In The Renal At Type 2 Diabetes Mellitus | en_US |
dc.type | Article | en_US |