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. 2023 Sep 27:14:1249234.
doi: 10.3389/fphar.2023.1249234. eCollection 2023.

Anti-inflammatory and analgesic effects of Streblus indicus

Affiliations

Anti-inflammatory and analgesic effects of Streblus indicus

Yan-Qing Xie et al. Front Pharmacol. .

Abstract

The bark of Streblus indicus, a Dai medicine in China, has been listed in the Chinese Materia Medica as possessing hemostatic and analgesic properties. Ethnic medicine books record that its bark or leaves for the treatment of mumps and lymphoma. However, according to the literature survey, anti-inflammatory and analgesic studies available for leaves and branches of S. indicus have been seldom reported so far. The current study focuses on the metabolites of S. indicus bark and leaves responsible for anti-inflammatory and analgesic effects on the basis of bioactive-included acetic acid writhing, hot-plate, and xylene-induced ear swelling. The secretion of inflammatory mediators, TNF-α, IL-6, IL-1β, IL-4, and IL-10, were evaluated for their anti-inflammatory by xylene-induced in mouse ear cells. Histological examination was used to assess the anti-inflammatory and analgesic effects of the branches and leaves of S. indicus, and Western blot analysis determined the mechanism of the methanolic extract of branches and leaves. Different metabolites of S. indicus significantly alleviated analgesic and anti-inflammatory effects, with no discernable differences among them. All metabolites decreased the levels of TNF-α, IL-1β, and IL-6 and increased the levels of IL-4 and IL-10. The analgesic and anti-inflammatory mechanism of the methanolic extract was related to the NF-kB signaling pathway. These results not only would account for scientific knowledge for the traditional application of S. indicus, but also provide a credible theoretical foundation for the further development of anti-inflammatory and analgesic agents.

Keywords: Streblus indicus (Bur.) Corner; analgesia; anti-inflammation; inflammatory cytokines; nuclear factor kappa B.

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Conflict of interest statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Figures

FIGURE 1
FIGURE 1
The results of acetic acid writhing test. (A) Number of turns in female mice. (B) Number of turns in male mice. *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001 compared with model group.
FIGURE 2
FIGURE 2
The results of xylene-induced ear swelling test. *p < 0.05, **p < 0.01, ***p < 0.001 compared with model group.
FIGURE 3
FIGURE 3
The results of inflammatory cytokines assay. *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001 compared with model group.
FIGURE 4
FIGURE 4
The results of histological examination analysis. (A) Histological alteration of the left ear in model group mice. (B) Histological alteration of the right ear in model group mice. (C) Histological alteration of the right ears from high dose group of methanolic extract of branches and leaves.
FIGURE 5
FIGURE 5
The results of NF-κB pathway in ear swelling anti-inflammatory test. The experimental groups were divided into blank control group (NC), model group (M) and high dose group of methanolic extract of branches and leaves (HMBL). In the figure, * is used to represent p values for NF-κB and IkBα groups, and # is used to represent p values for p-NF-κB and p-IkBα groups. Compared with M group, # and * represent p < 0.05, ## and ** represent p < 0.01, ### and *** represents p < 0.001, #### and **** means p < 0.0001.
FIGURE 6
FIGURE 6
The results of Cytotoxicity test. (A) Cytotoxicity test results of different dosages of bark methanolic extract group. (B) Cytotoxicity test results of different dosages of bark aqueous extract group. (C) Cytotoxicity test results of different dosages of branches and leaves methanolic extract group. (D) Cytotoxicity test results of different dosages of branches and leaves aqueous extract group. NC was blank control group. *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001 compared with model group.

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