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Risyifa Audinia
"ABSTRAK
Penyakit ginjal diabetes merupakan salah satu penyebab utama gagal ginjal stadium akhir, sehingga dibutuhkan penanda biologis yang spesifik dan sensitif untuk mengantisipasi progresi penyakit. Sistem renin-angiontensin aldosteron diketahui memiliki peran yang signifikan dalam perkembangan awal penyakit ginjal diabetes, sehingga renin sebagai salah satu komponen sistem renin-angiotensin aldosteron memiliki potensi sebagai penanda awal penyakit ginjal diabetes. Penulisan review article ini bertujuan untuk mengkaji literatur-literatur terkini yang meneliti hubungan kadar renin pada urin dengan perkembangan kerusakan ginjal. Review bersifat sistematik berdasarkan acuan Preferred Reporting Items for Systematic Reviews and Meta-Analyses Guidelines (PRISMA) tahun 2009 dengan pendekatan kualitatif. Literatur yang dikaji diperoleh melalui pencarian internet pada database ScienceDirect, PubMed, dan SpringerLink. Sebanyak 5 literatur dipilih berdasarkan kriteria yang ditetapkan. Hasil analisis literatur menunjukkan bahwa potensi renin urin sebagai penanda biologis penyakit ginjal diabetes cukup besar dikarenakan renin urin akan meningkat pada kondisi kerusakan ginjal. Selain itu, renin urin juga dapat menggambarkan aktivitas sistem renin-angiotensin aldosteron intrarenal dan memiliki korelasi positif dengan albuminuria. Hasil analisis literatur juga menunjukkan bahwa tidak adanya korelasi antara eLFG dan renin urin pada pasien dengan penyakit ginjal diabetes. Namun, renin urin secara signifikan lebih tinggi pada pasien dengan penyakit ginjal diabetik dibandingkan dengan pasien dengan penyakit ginjal kronis.

ABSTRACT
Diabetic kidney disease is one of the main causes of end-stage renal disease, therefore there is a need for specific and sensitive biological markers to anticipate progression of the disease. The renin-angiontensin aldosterone is known to have a significant role in the early development of diabetic kidney disease, that means renin as one of the components of the renin-angiotensin aldosterone system has a potential as an early biomarker for diabetic kidney disease. This review article aims to review latest literatures that studied the relationship of renin levels in urine with the development of kidney damage in patients with diabetes or chronic kidney disease. This systematic review was written based on the Reference Reporting Item Options for Systematic Review and Meta-Analysis Guide (PRISMA) of 2009 with a qualitative approach. The literature studied was obtained through an internet search in the ScienceDirect, PubMed, and SpringerLink databases. A total of 5 literatures were chosen based on specified criteria. The results of the literature analysis showed that urinary renin has a promising potential as a biological marker for diabetic kidney disease because urinary renin will likely increase in presence kidney damage. In addition, urinary renin can also describe the activity of the intrarenal renin-angiotensin aldosterone system and positively corelates with albuminuria. The results of the literature analysis also showed no correlations between eGFR and urinary renin in patients with diabetic kidney disease. However, urinary renin were significantly high in patients with diabetic kidney disease compared to patients with chronic kidney disease."
Depok: Fakultas Farmasi Universitas Indonesia, 2020
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UI - Skripsi Membership  Universitas Indonesia Library
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Shinta Ayu Nurfaradilla
"Ekstrak air Hibiscus sabdariffa (HS) telah digunakan sebagai pengobatan tradisional pada terapi hipertensi. Banyak orang menggabungkan penggunaan ekstrak air HS dengan kaptopril sehingga dapat berpotensi menimbulkan interaksi. Penelitian ini bertujuan untuk mengetahui pengaruh koadministrasi ekstrak air HS terhadap profil farmakokinetika kaptopril, tekanan darah, dan biomarkersistem renin angiotensin aldosteron (RAAS). Studi farmakokinetika dilakukan terhadap empat kelompok tikus (n = 6). Kelompok I menerima suspensi kaptopril tunggal (CAP; 4,5 mg/200 g BB) sementara kelompok II, III, dan IV menerima koadministrasi ekstrak air HS (15 mg/200 g BB, 30 mg/200 g BB, dan 60 mg/200g BB) dan kaptopril 4,5 mg/200 g BB. Untuk pengukuran tekanan darah dan level biomarker RAAS, digunakan tujuh kelompok tikus (n = 6) berbeda yang terdiri dari satu kelompok sham dan enam kelompok tikus model 2K1C. Pada tikus model 2K1C, hipertensi diinduksi dengan pemasangan mikroklip stainless steel (ID: 0,20 mm) pada arteri ginjal kiri. Kelompok tikus model terdiri dari kontrol negatif (2K1C, tidak diobati), kontrol positif (4,5 mg/200 g BB kaptopril), ekstrak air HS tunggal (30 mg/200 g BB), dan 3 kelompok koadministrasi yang menerima ekstrak air HS (15, 30, atau 60 mg/200g BB) dan kaptopril 4,5 mg/200 g BB. Pemberian ekstrak dan kaptopril dilakukan secara peroral. Seluruh perlakuan dilakukan selama 2 minggu. Ketiga dosis koadministrasi ekstrak HS dapat mempengaruhi profil farmakokinetika kaptopril secara signifikan. Nilai AUC0-t, AUC0-, dan Cmax, pada kelompok tersebut mengalami penurunan, sementara nilai Cl/F dan Vd/F mengalami peningkatan. Seluruh pemberian terapi pengobatan menyebabkan penurunan tekanan darah secara signifikan mendekati kelompok sham. Level renin plasma, aktivitas serum angiotensin converting enzyme (ACE), dan level angiotensin II plasma pada kelompok 2K1C mengalami kenaikan yang signifikan dibandingkan dengan kelompok sham. Aktivitas serum ACE dan level angiotensin II plasma pada seluruh kelompok terapi mengalami penurunan signifikan dan nilainya mendekati kelompok sham. Ekstrak air HS tunggal dapat menurunkan tekanan darah, namun koadministrasi dengan kaptopril tidak memberikan efek tambahan. Oleh karena itu, dapat disimpulkan bahwa pemberian koadministrasi ekstrak air HS dengan kaptopril dapat mempengaruhi profil farmakokinetika kaptopril secara signifikan, namun tidak memberikan pengaruh yang signifikan terhadap penurunan tekanan darah dan level biomarker RAAS.

Hibiscus sabdariffa (HS) extract has been used as traditional medicine during management of hypertension. Many people co-administered HS aqueous extract with captopril thus predispose herb-drug interaction. The purpose of this study was to determine the effect of HS aqueous extract co-administration on the pharmacokinetic profile of captopril, blood pressure, and biomarker level of renin angiotensin aldosterone system (RAAS). Pharmacokinetic study was performed on four groups of rats (n = g). Group I received captopril suspension only (CAP; 4.5 mg/200 g BW), while group II, III, and IV received co-administration of Hibiscus sabdariffa extract (15 mg/200 g BW, 30 mg/200 g BW, and 60 mg/200 g BW respectively) and captopril 4.5 mg/200 g BW. Blood pressure and biomarker level of RAAS measurement were performed on another 7 groups (n = 6), a SHAM group and six 2K1C groups. In 2K1C animals, hypertension was induced by placing a stainless micro clip (inner diameter of 0.20 mm) on left renal artery. The 2K1C animals consist of negative control (2K1C, no treatment), positive control (captopril 4.5 mg/200 g BW), HS aqueous extract (30 mg/200 g BW), and three co-administration groups receiving HS aqueous extract (15, 30, or 60 mg/200 g BW) plus 4.5 mg/200 g BW captopril. Extract and captopril administration were given by oral gavage. All treatments were performed for two weeks. Pharmacokinetic profile of captopril was changed significantly by all co-administration doses of HS aqueous extract. The AUC0-t, AUC0-, and Cmax value of those groups were decreased, conversely the Cl/F and Vd/F value were increased. Blood pressure was significantly reduced by all the drug treatments approaching the level of SHAM controls. Plasma renin level, serum angiotensin converting enzyme (ACE) activity, and plasma angiotensin II level were also significantly elevated in the 2K1C group compared to the SHAM group. Both serum ACE activity and plasma angiotensin II level were significantly reduced approaching the SHAM group levels by all the drug treatments. HS aqueous extract can reduce blood pressure but may not provide any additional benefit. Therefore, we can conclude that co-administration of HS aqueous extract with captopril could affect the pharmacokinetic profile significantly, however it didnt have significant effect on the decrease in blood pressure and RAAS biomarker level.
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Depok: Fakultas Farmasi Universitas Indonesia, 2019
T53603
UI - Tesis Membership  Universitas Indonesia Library