4.7 Article

Chaihu Guizhi Ganjiang Decoction Ameliorates Pancreatic Fibrosis via JNK/mTOR Signaling Pathway

Journal

FRONTIERS IN PHARMACOLOGY
Volume 12, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fphar.2021.679557

Keywords

Chaihu Guizhi Ganjiang Decoction; chronic pancreatitis; pancreatic stellate cells; autophagy; JNK; mTOR

Funding

  1. Key Research Lab of the State Administration of Traditional Chinese Medicine (DYBT)
  2. Scientific Research Project of Integrated Traditional Chinese and Western Medicine of Tianjin Municipal Health Committee [2019037]
  3. Scientific Research Projects in Key Areas of Traditional Chinese Medicine of Tianjin Municipal Health Committee [2019004]
  4. National Natural Science Foundation of China [82004147]
  5. Scientific and Technological Personnel Training Project of Tianjin Municipal Health Committee [RC20157]

Ask authors/readers for more resources

Chaihu Guizhi Ganjiang Decoction (CGGD) showed effects in alleviating pancreatic damage, reducing collagen deposition, and inhibiting pancreatic stellate cell (PSC) activation in a rat model of chronic pancreatitis. By suppressing autophagy in PSCs through the JNK/mTOR signaling pathway, CGGD attenuated pancreatic fibrosis and PSC activation.
Pancreatic fibrosis is a pathological characteristic of chronic pancreatitis (CP) and pancreatic cancer. Chaihu Guizhi Ganjiang Decoction (CGGD) is a traditional Chinese medicine, which is widely used in the clinical treatment of digestive diseases. However, the potential anti-fibrosis mechanism of CGGD in treating CP remains unclear. Here, we conducted a series of experiments to examine the effect of CGGD on the CP rat model and primary isolated pancreatic stellate cells (PSCs). The results revealed that CGGD attenuated pancreatic damage, decreased collagen deposition, and inhibited PSC activation in the pancreas of CP rats. However, compared with the CP group, CGGD had no effect on body weight and serum amylase and lipase. In addition, CGGD suppressed autophagy by downregulating Atg5, Beclin-1, and LC3B and facilitated phosphorylation of mTOR and JNK in pancreatic tissues and PSCs. Moreover, the CGGD-containing serum also decreased LC3B or collagen I expression after rapamycin (mTOR inhibitor) or SP600125 (JNK inhibitor) treatment in PSCs. In conclusion, CGGD attenuated pancreatic fibrosis and PSC activation, possibly by suppressing autophagy of PSCs through the JNK/mTOR signaling pathway.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available