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 |