Objective

2

To explore the anti-tumor effect and mechanism of Shenqi Yiliu prescription in the intervention of pyroptosis.

Method

2

Ten male BALB/c mice were randomly selected and assigned to the blank group. The remaining 40 mice underwent the induction of the liver cancer xenograft model. After 5 days of modeling， 40 surviving mice were randomly divided into model group， cisplatin group ［2.5×10

-3

g·kg

-1

·（3 d）

-1

］， Shenqi Yiliu prescription group （27 g·kg

-1

·d

-1

）， and a combination group （Shenqi Yiliu prescription group + cisplatin）. The mice in the blank group and the model group were treated with an equal volume of normal saline for 10 days. The general conditions of mice in each group were observed. After the intervention， the tumor weight of the mice was weighed and the tumor inhibition rate was calculated. Hematoxylin-eosin （HE） staining was used to observe the pathological changes in tumor tissues. The levels of mouse liver function indicators， including alanine aminotransferase （ALT） and aspartate aminotransferase （AST） were detected. The TdT-mediated dUTP-biotin nick end labeling （TUNEL） assay was used to detect DNA damage in mouse tumor tissue cells. Immunohistochemistry （IHC）， immunofluorescence （IF）， and Western blot were used to detect the protein expression levels of NOD-like receptor protein 3 （NLRP3）， cysteinyl aspartate-specific protease-1 （Caspase-1）， and gasdermin D （GSDMD） in tumor tissues. The levels of interleukin-1

β

（IL-1

β

） and interleukin-18 （IL-18） in tumor tissues were detected by enzyme-linked immunosorbent assay （ELISA）.

Result

2

Compared with the mice in the blank group， those in the model group were in a poor mental state， sleepy， and lazy， and their fur color was dull， with increased levels of serum ALT and AST in liver function tests （

P

<

0.01）. Compared with the model group， the groups with drug intervention showed improved mental state， inhibited tumor growth to varying degrees， and decreased tumor weight， and the tumor inhibition rate in the combination group was the highest （

P

<

0.01）. HE staining showed that the pathological and morphological lesions of the tumor tissues in the model group were significant， while those in all groups with drug intervention were improved to a certain extent. The karyolysis and nuclear rupture in the Shenqi Yiliu prescription group and the combination group were more significant. In the liver function test， the serum ALT and AST levels of mice in the Shenqi Yiliu prescription group and the combination group decreased （

P

<

0.01）， and the inflammatory factors IL-1

β

and IL-18 in each group with drug intervention decreased （

P

<

0.05，

P

<

0.01）. Among them， the declining trend of IL-1

β

and IL-18 in the Shenqi Yiliu prescription group was the most significant （

P

<

0.01）. TUNEL staining showed that the positive TUNEL staining in each group with drug intervention decreased after intervention （

P

<

0.05，

P

<

0.01）， especially the cisplatin group and Shenqi Yiliu prescription group （

P

<

0.01）. Western blot， IHC， and IF found that the protein expression levels of NLRP3， Caspase-1， and GSDMD in each group with drug intervention decreased （

P

<

0.05，

P

<

0.01）. Compared with the mice in the cisplatin group， those in the Shenqi Yiliu prescription group and the combination group had better mental state and regular tumor morphology， and the tumor weight of the mice in the combination group decreased （

P

<

0.05）. The levels of ALT and AST in the Shenqi Yiliu prescription group decreased （

P

<

0.05）， and the levels of IL-1

β

and IL-18 in the Shenqi Yiliu prescription group and the combination group decreased （

P

<

0.05，

P

<

0.01）， especially in the combination group （

P

<

0.01）. The results of IHC showed that the expression of GSDMD protein in the tumor tissues of mice in the combination group was reduced （

P

<

0.01）. IF detection showed that the expression of NLRP3 in the tumor tissues of the Shenqi Yiliu prescription group was reduced （

P

<

0.01）. The results of Western blot showed that the expression level of NLRP3 protein in the Shenqi Yiliu prescription group and the combination group decreased （

P

<

0.01）， and the expression level of Caspase-1 protein in the combination group decreased （

P

<

0.01）. The decrease in GSDMD protein expression was not significant， and the difference was not statistically significant.

Conclusion

2

Shenqi Yiliu prescription combined with cisplatin has an obvious anti-tumor effect， which may be achieved by down-regulating the NLRP3/Caspase-1/GSDMD inflammatory pyroptosis pathway to inhibit cell pyroptosis， and relieve the inflammatory response in mice with liver cancer.