The Effects of Interferon α2b on Chemically-Induced Peritoneal Fibrosis and on Peritoneal Tissue MMP-2 and TIMP-2 Levels in Rats

Author:

Ucar E1,Borazan A1,Semerci E2,Binici DN3,Yaldiz M4,Aysal A5,Altug E6,Kuvandik C7,Huzmeli C1,Yetim T1,Canda S4

Affiliation:

1. Department of Nephrology, Erzurum Education and Research Hospital, Erzurum, Turkey

2. Department of General Surgery, Erzurum Education and Research Hospital, Erzurum, Turkey

3. Department of Internal Medicine, Erzurum Education and Research Hospital, Erzurum, Turkey

4. Department of Pathology, Mustafa Kemal University, Hatay, Turkey

5. Department of Pathology, Dokuz Eylul University, Izmir, Turkey

6. Department of General Surgery, Faculty of Veterinary Medicine, Mustafa Kemal University, Hatay, Turkey

7. Department of Infectious Disease, Kırıkhan Government Hospital, Hatay, Turkey

Abstract

This study investigated the effect of interferon α2b on chlorhexidine gluconate (CH)-induced peritoneal fibrosis (PF) in rats and assessed peritoneal tissue levels of metalloproteinase (MMP)-2 and tissue inhibitors of metalloproteinases (TIMP)-2. Wistar albino rats ( n = 8 per group) were treated as follows: control group, 3 ml/day of 0.9% saline intra-peritoneally for 28 days; CH group, 0.1% CH (200 g [3 ml]/day) in 15% ethanol and 0.9% saline intra-peritoneally for 28 days; CH + interferon (IFN) group, CH (as above) plus pegylated IFN-α2b 1.5 μg/kg per week subcutaneously on days 0, 7, 14, 21 and 28; IFN group, pegylated IFN-α2b (as above). Parietal peritoneum samples were obtained from the left anterior abdominal wall after 35 days. Parietal thickness, degree of vascular proliferation and inflammation, and MMP-2 and TIMP-2 levels were determined. The mean peritoneal thicknesses of the control, CH, CH + IFN and IFN groups were 7.02 ± 3.89, 156.86 ± 29.13, 59.88 ± 22.1, 9.27 ± 2.03 μm, respectively. Pegylated IFN-α2b decreased CH-induced expression of MMP-2 in the parietal peritoneum, but had no effect on TIMP-2 levels. Further studies are needed to determine the optimal dosage and duration for pegylated IFN-α2b treatment.

Publisher

SAGE Publications

Subject

Biochemistry (medical),Cell Biology,Biochemistry,General Medicine

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