Effect of pyrrolidine dithiocarbamate on expression of E-selectin and oxidative stress related enzymes in rats with severe acute pancreatitis induced by L-arginine
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Effect of pyrrolidine dithiocarbamate on expression of E-selectin and oxidative stress related enzymes in rats with severe acute pancreatitis induced by L-arginine
Journal of Army Medical UniversityVol. 31, Issue 8, Pages: 697-700(2009)
作者机构:
第三军医大学新桥医院消化内科
作者简介:
基金信息:
DOI:
CLC:R576.05;R965;R446.8
Published:2009,
Published Online:30 April 2009,
稿件说明:
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LE XIANG-HUA, WANG LEI, ZHAO XIAO-YAN. Effect of pyrrolidine dithiocarbamate on expression of E-selectin and oxidative stress related enzymes in rats with severe acute pancreatitis induced by L-arginine. [J]. Journal of army medical university, 2009, 31(8): 697-700.
DOI:
LE XIANG-HUA, WANG LEI, ZHAO XIAO-YAN. Effect of pyrrolidine dithiocarbamate on expression of E-selectin and oxidative stress related enzymes in rats with severe acute pancreatitis induced by L-arginine. [J]. Journal of army medical university, 2009, 31(8): 697-700.DOI:
Effect of pyrrolidine dithiocarbamate on expression of E-selectin and oxidative stress related enzymes in rats with severe acute pancreatitis induced by L-arginine
ithiocarbamate (PDTC) on the expression of E-selectin and the activities of enzymes in oxidative stress in the pancreas of rats with severe acute pancreatitis (SAP). Methods Rat model of ASP was build by intraperitoneal injection of L-arginine (totally 5 g/kg
twice in an interval of 1 h). Thirty-six SD rats were assigned to 6 groups randomly and equally
that is
normal control
SAP
PDTC pretreatment group 1 (1 mg/kg) and 2 (100 mg/kg)
and PDTC treatment group 1 (1 mg/kg) and 2 (100 mg/kg). PDTC pretreatment was preformed by subcutaneous injection of PDTC 1 h before first injection of L-arginine. For the animals in treatment groups
PDTC was given 3 h after first injection. Normal control was given intraperitoneal injection of normal saline. In 24 h after the first injection of L-arginine
the activity of myeloperoxidase (MPO)
lipid peroxide (LPO) and nitric oxide synthase (NOS) were detected. Expressions of E-selectin was detected through inmmunohistochemical method
and activity of NF-κB-DNA binding were detected by electrophoretic mobility shift assay (EMSA). Results In SAP groups and PDTC pretreatment and treatment groups
the expression of E-selectin
activities of NF-κB
MPO
LPO
and inducible NOS (iNOS) were higher
but the activity of constitutive NOS (cNOS) was lower than those in the normal control (
P
<
0.05). PDTC treatment group 1 had comparatively lower above increased items
but higher activity of cNOS in comparison with SAP group (
P
<
0.05)
and PDTC pretreatment group 1 was more significant (
P
<
0.01). However
PDTC at the dosage of 100 mg/kg no matter before or after L-arginine injection had few effects on all above items compared to SAP group (
P
>0.05). Conclusion PDTC of 1 mg/kg can alleviate the inflammation in SAP by blocking the translocation of NF-κB
however
the 100 mg/kg PDTC shows little protection in this process.