YANG Hong,REN Pengyan,CHEN Yongxin,et al.Interventional effect and mechanism of 1,8-cineoleon pancreatic β cell ferroptosis induced by type 2 diabetes[J].ZHONGGUO YAOFANG,2024,35(03):290-295.
YANG Hong,REN Pengyan,CHEN Yongxin,et al.Interventional effect and mechanism of 1,8-cineoleon pancreatic β cell ferroptosis induced by type 2 diabetes[J].ZHONGGUO YAOFANG,2024,35(03):290-295. DOI: 10.6039/j.issn.1001-0408.2024.03.05.
Interventional effect and mechanism of 1,8-cineoleon pancreatic β cell ferroptosis induced by type 2 diabetes
To study the interventional effect and mechanism of 1,8-cineole on pancreatic β cell ferroptosis induced by type 2 diabetes.
METHODS
2
In vitro
ferroptosis model was established in pancreatic β cells of mice by using high glucose. The effects of low-dose and high-dose 1,8-cineole (0.25, 0.5 μmol/L) on the level of Fe
2+
in pancreatic β cells were investigated. The effects of 1,8-cineole (0.5 μmol/L) combined with ferroptosis inducer Erastin (20 μmol/L) and ferroptosis inhibitor Ferrostatin-1 (20 μmol/L) on the protein expressions of glutathione peroxidase-4 (GPX4) and cyclooxygenase-2 (COX2) were also detected. The type 2 diabetes model mice were established by feeding high-sugar and high-fat diet combined with intraperitoneal injection of streptozotocin. The effects of low-dose and high-dose 1,8-cineole (50, 200 mg/kg) on the pathological morphology of pancreatic tissue, the content of iron as well as the protein expressions of GPX4 and COX2 were investigated.
RESULTS
2
The results of the cell experiment showed that compared with the model group, pretreatment with 1,8-cineole significantly reduced intracellular Fe
2+
levels and upregulated GPX4 protein expression, while downregulated COX2 protein expression in pancreatic β cells (
P
<0.05). After combining with Ferrostatin-1, the expression trends of the above two proteins were the same, while there was no statistically significant difference after combining with Erastin. The results of anima
l experiments showed that compared with the model group, after intervention with 1,8-cineole, the structure of the pancreatic islets in mice recovered intact and their morphology improved; the iron content of pancreatic tissue and protein expression of COX2 were decreased significantly (
P
<0.05), while protein expression of GPX4 was increased significantly (
P
<0.05).
CONCLUSIONS
2
1,8-cineole could ameliorate pancreatic β cell injury induced by diabetes, the mechanism of which may be related to reducing intracellular iron deposition and regulating ferroptosis-related proteins.
关键词
Keywords
references
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Related Institution
School of Chinese Materia Medica, Guangdong Pharmaceutical University/Guangdong Engineering Technology Research Center for Standardized Processing of Chinese Materia Medica
Heilongjiang Key Laboratory for Pharmacodynamic Material Bases of TCM and Natural Medicines/Key Laboratory of Northern Medicine Foundation and Application,Ministry of Education,Heilongjiang University of Chinese Medicine
Dept. of Nephrology, the Affiliated Hospital of Southwest Medical University/Nephropathy Clinical Medical Research Center of Sichuan Province
Research Center of Traditional Chinese Medicine and Western Medicine Integration,the Affiliated Traditional Chinese Medicine Hospital of Southwest Medical University
Dept. of Nephrology, the Affiliated Chinese Traditional Medicine Hospital of Southwest Medical University