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Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie 2018-Apr

Therapeutic effects of Saussurea involucrata injection against severe acute pancreatitis- induced brain injury in rats.

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Xiaohong Wang
Lei Chu
Chun Liu
Ronglong Wei
Xianglong Xue
Yuefen Xu
Mengjie Wu
Qing Miao

Keywords

Abstract

OBJECTIVE

To observe the therapeutic effects of Saussurea involucrata (Sau) injection against severe acute pancreatitis (SAP)-induced brain injury.

METHODS

Sodium taurocholate-induced SAP-modeled rats were equally randomized into an SAP model group (SAP group) and a Sau treated group (Sau + S group). Healthy rats were equally randomized into a Sau treated group (Sau + H group) and a sham operation group (SO group). Serum amylase levels, endothelin-1 (ET-1) and nitric oxide (NO) contents were determined by optical turbidimetry, ELISA and nitrate reductase method respectively. Western blot was used to detect protein expression levels of phosphatidylinositol 3-kinase (PI3K), protein kinase B (Akt), ET-1, inducible nitric oxide synthase (iNOS) and endothelial NOS (eNOS) while mRNA levels of these biomarkers in brain tissue were measured by quantitative real-time PCR. Furthermore, pathological changes, as well as all above indexes of pancreas and brain, were observed at 6, 24 and 48 h after administration.

RESULTS

There was a significant difference in mortality between SAP and Sau + S groups (P < 0.05). Serum amylase levels, ET-1 and NO contents, ET-1/NO ratio, relative expression levels of ET-1 and iNOS protein/mRNA of brain tissue in Sau + S group were lower than those in SAP group at 24 and 48 h post-operation (P < 0.05 or 0.01), meanwhile, pancreas and brain pathological scores showed similar tendency (P < 0.01). However, both protein and mRNA levels of PI3K, Akt and eNOS of brain tissue in Sau + S group were higher than those in SAP group (P < 0.05 or P < 0.01). There were no significant differences in all indexes between Sau + H and SO groups at all designated time points (P > 0.05).

CONCLUSIONS

Sau injection has therapeutic effects on SAP-induced brain injury in rats.

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