The effects of pentoxifylline and caffeic acid phenethyl ester on TNF-? and lung histopathology in D-galactosamine-induced pulmonary injury in rats

被引:4
作者
Taslidere, Elif [1 ]
Vardi, Nigar [1 ]
Yildiz, Azibe [1 ]
Ates, Burhan [2 ]
Esrefoglu, Mukaddes [3 ]
机构
[1] Inonu Univ, Fac Med, Dept Histol & Embryol, Malatya, Turkiye
[2] Inonu Univ, Dept Chem, Malatya, Turkiye
[3] Bezmialem Vakif Univ, Fac Med, Dept Histol & Embryol, Istanbul, Turkiye
关键词
Galactosamine; Pentoxifylline; Caffeic acid phenethyl ester; Lung; Rat; NECROSIS-FACTOR-ALPHA; ISCHEMIA-REPERFUSION; OXIDATIVE STRESS; LIVER-INJURY; KAPPA-B; INFLAMMATION; APOPTOSIS; PROPOLIS; MODEL; PATHOGENESIS;
D O I
10.1016/j.tice.2023.102085
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
In this study, we aimed to investigate the effects of pentoxifylline [PTX] and caffeic acid phenethyl ester [CAPE] in D-galactosamine [D-GAL]-induced pulmonary injury in rats. The rats were randomly divided into six groups: control, D-GAL, D-GAL+PTX, D-GAL+CAPE, PTX and CAPE. Each group included eight animals. Lung sections from the control, PTX and CAPE groups had a normal histological appearance. The D-GAL group showed histopathological changes in lung tissue, including haemorrhage, oedema, inter-alveolar septal thickening and widespread infiltration of inflammatory lymphocytes and macrophages. Administration of PTX and CAPE significantly reduced histopathological damage scores in the D-GAL+PTX and D-GAL+CAPE groups compared with the D-GAL group. PTX and CAPE treatment also significantly decreased malondialdehyde levels, increased levels of reduced GSH and increased catalase and superoxide dismutase activity in lung tissue samples. These results indicate that the destructive effects of D-GAL-induced inflammation in the rat lung are significantly reduced following administration of PTX and CAPE.
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页数:7
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