Analisis Ekspresi Vimentin pada Hati Babi yang Diinduksi Sirosis oleh Diethylnitrosamine dan Phenobarbital.
Date
2026Jenis/Type
SkripsiSubtype
Undergraduate ThesesAuthor
Abimanyu, Arkhana Prasetyo
Juniantito, Vetnizah
Novelina, Savitri
Metadata
Show full item recordAbstract
ARKHANA PRASETYO ABIMANYU. Analisis Ekspresi Vimentin pada Hati
Babi yang Diinduksi Sirosis oleh Diethylnitrosamine dan Phenobarbital. Dibimbing oleh VETNIZAH JUNIANTITO dan SAVITRI NOVELINA. Sirosis hati merupakan kerusakan hati tahap lanjut yang ditandai fibrosis
ekstensif dan nodul regeneratif. Model babi dipilih karena kemiripan anatomi dan
fisiologi hatinya dengan manusia. Penelitian ini menganalisis ekspresi
vimentinpenanda sel mesenkimal terkait aktivasi hepatic stellate cells (HSC) pada
hati babi yang diinduksi sirosis menggunakan DENA dan phenobarbital, melalui
pewarnaan HE, Azan-Mallory, dan Immunohistokimia. Hasil menunjukkan
perubahan histopatologi berupa septa fibrotik, nodul regeneratif, dan deposisi
kolagen di area septa, perivaskuler, dan perisinusoidal. Ekspresi vimentin
dominan ditemukan di area tersebut dengan morfologi sel spindle-shaped, mengindikasikan aktivasi sel mesenkimal dan fibrogenesis aktif selama
perkembangan sirosis. Temuan ini relevan sebagai acuan pengembangan
diagnostik dan terapi penyakit hati kronis pada manusia. ARKHANA PRASETYO ABIMANYU. Analysis of Vimentin Expression in
Swine Liver Cirrhosis Induced by Diethylnitrosamine and Phenobarbital. Supervised by VETNIZAH JUNIANTITO and SAVITRI NOVELINA. Liver cirrhosis is an advanced stage of liver damage characterized by
extensive fibrosis and regenerative nodules. The pig model was selected due to its
anatomical and physiological similarities to the human liver. This study analyzed
the expression of vimentin a mesenchymal cell marker associated with hepatic
stellate cell (HSC) activationin pig livers induced with cirrhosis using DENA and
phenobarbital, through HE staining, Azan-Mallory, and immunohistochemistry. Results showed histopathological changes including fibrous septa formation, regenerative nodules, and collagen deposition in septal, perivascular, and
perisinusoidal areas. Vimentin expression was predominantly found in these areas
with spindle-shaped cell morphology, indicating active mesenchymal cell
activation and fibrogenesis during cirrhosis progression. These findings provide a
relevant vimentin expression profile in a large animal model for the development
of diagnostic and therapeutic approaches for chronic liver disease in humans.

