Chlorogenic Acid Alleviates Chronic Stress-Induced Intestinal Damage by Inhibiting the P38MAPK/NF-κB Pathway

• Published in: Journal of agricultural and food chemistry Vol. 71; no. 24; pp. 9381 - 9390
• Main Authors: Zhao, Yuan, Wang, Chaoran, Yang, Tianyuan, Feng, Guofeng, Tan, Haoyang, Piao, Xue, Chen, Dongni, Zhang, Yu, Jiao, Wenjign, Chen, Yongping, Sha, Jichen, Fan, Honggang
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 21.06.2023
• Subjects: Animals; Bioactive Constituents, Metabolites, and Functions; Chlorogenic Acid; food chemistry; gene expression; intestines; intraperitoneal injection; NF-kappa B - metabolism; occludins; p38 Mitogen-Activated Protein Kinases - genetics; polyphenols; Rats; Rats, Wistar; tight junctions; Tumor Necrosis Factor-alpha; NF-κB; chronic stress; intestinal barrier; chlorogenic acid; P38MAPK
• ISSN: 0021-8561; 1520-5118; 1520-5118
• DOI: 10.1021/acs.jafc.3c00953

Chronic stress can cause intestinal barrier damage. MAPK and NF-κB are closely related to it. Chlorogenic acid (CGA), a dietary polyphenol, has been shown to have intestinal protective effects, but whether by regulating MAPK and NF-κB is not known. Therefore, in this experiment, 24 Wistar rats were randomly divided into 4 groups (C group, CS group, CS + SB203580, and CS + CGA group). Rats in the CS group were restrained stress for 6 h per day for 21 days. Rats in the CS + SB203580 group were given SB203582 (0.5 mg/kg, intraperitoneal injection) 1 h before restraint stress every other day. Rats in the CS + CGA group were given CGA (100 mg/kg, gavage) 1 h before restraint stress. In chronic stress, intestinal barrier damage was evident, while being restored after CGA treatment. After chronic stress, the levels of p-P38 were increased (P < 0.01), while the levels of p-JNK and p-ERK were not changed. The levels of p-p38 were elevated after CGA treatment (P < 0.01). These results suggested that p38MAPK played an important role in chronic stress-induced intestinal injury, and CGA could inhibit p38MAPK activity. Therefore, we chose SB203582 (P38MAPK inhibitor) to elucidate the role of p38. After chronic stress, intestinal tight junction key proteins Occludin, ZO-1, and Claudin3 protein and gene expression were reduced (P < 0.01), while being elevated after CGA or SB203582 intervention (P < 0.05). After CGA treatment, the levels of p-IκB, p-p65, p-p38, and TNF-α were reduced (P < 0.01). SB203582 intervention reduced p-p65 and TNF-α levels significantly (P < 0.01). These results suggested that CGA could inhibit the NF-κB pathway by suppressing p38MAPK, thereby alleviating chronic stress-induced intestinal damage.