Antioxidative effect of Periplaneta americana extract on dextran sulfate sodium-induced ulcerative colitis through activation of the Nrf2 signal

Pharm Biol. 2023 Dec;61(1):949-962. doi: 10.1080/13880209.2023.2220351.

Abstract

Context: Periplaneta americana L. (Blattariae) is used as a treatment for ulcerative colitis (UC) in Chinese traditional medicine.

Objective: To evaluate the antioxidative activity of P. americana whole body ethanol extract (PAE) on UC mice and whether glycine and proline could be used for quality control and identification of active PAE components.

Materials and methods: NCM460 cells were pre-incubated in PAE, AA-L, AA-M, and AA-H (low, high and medium doses of proline and glycine), then treated with recombinant human TNF-α. The glutathione (GSH), malondialdehyde (MDA), superoxide dismutase (SOD) and reactive oxygen (ROS) levels were determined. UC mice were fed with water containing 2.5% dextran sulfate sodium (w/v) after pre-treatment with different doses of PAE once a day for 7 days. ELISA was used to detect the concentrations of inflammation-related factors. Colon tissues of mice were used to detect the activity of myeloperoxidase (MPO), GSH, MDA, and SOD. Histological changes were observed using H&E staining. The expression of target proteins was determined by western blotting.

Results: In vivo, PAE treatment reduced the DAI score more than in the model group, restoring the weight and colonic length. It also reduced the severity of colitis, and inflammatory and oxidative stress intensity. Additionally, western blotting showed that the Nrf2 pathway was activated by PAE. In vitro PAE significantly alleviated TNF-α-induced cell damage and oxidative stress, which is relevant to the activation of the Nrf2 pathway.

Conclusions: PAE may relieve oxidative stress through the Nrf2 signaling pathway, and proline and glycine may be used as active components of its antioxidative stress activity.

Keywords: Amino acids; anti-inflammatory; natural animal extracts.

MeSH terms

  • Animals
  • Antioxidants / therapeutic use
  • Colitis, Ulcerative* / chemically induced
  • Colitis, Ulcerative* / drug therapy
  • Colitis, Ulcerative* / metabolism
  • Colon
  • Dextran Sulfate / toxicity
  • Disease Models, Animal
  • Humans
  • Mice
  • NF-E2-Related Factor 2 / metabolism
  • Periplaneta* / metabolism
  • Superoxide Dismutase / metabolism
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Antioxidants
  • Dextran Sulfate
  • NF-E2-Related Factor 2
  • Tumor Necrosis Factor-alpha
  • Superoxide Dismutase

Grants and funding

This study was supported by several grants as follows: the National Natural Science Fund of China under Grant (NO. 82060780); Yunnan Fundamental Research Projects under Grant (NO. 2019FH001-003, 202001AT070021, 202305AC160034); the Program for Innovative Research Team of Yunnan Province: Traditional entomic medicine effective substances discovery and comprehensive utilization under Grant [NO. 202305AS350001]; and the Special Program of Science and Technology of Yunnan Province under Grant (NO. 202002AA100007).