Antinociceptive and anti-inflammatory activities of butein in different nociceptive and inflammatory mice models

被引:11
|
作者
Gao, Li [1 ]
Cui, Shasha [2 ]
Huang, Zhiqiang [3 ]
Cui, Hailong [4 ]
Alahmadi, Tahani Awad [5 ,6 ]
Manikandan, Velu [7 ]
机构
[1] Jiamusi Univ, Affiliated Hosp 1, Dept Anesthesiol, Jiamusi 154002, Heilongjiang, Peoples R China
[2] Jincheng Peoples Hosp, Dept Anesthesiol, Jincheng 048000, Shanxi, Peoples R China
[3] Xilingo League Cent Hosp, Dept Anesthesiol, Xilingo League 026000, Inner Mongolia, Peoples R China
[4] Hohhot Maternal & Child Hlth Hosp, Dept Anesthesiol, Hohhot 010031, Inner Mongolia, Peoples R China
[5] King Saud Univ Med City, Dept Pediat, Coll Med, POB 2925, Riyadh 11461, Saudi Arabia
[6] King Saud Univ Med City, King Khalid Univ Hosp, POB 2925, Riyadh 11461, Saudi Arabia
[7] Jeonbuk Natl Univ, Coll Environm & Bioresource Sci, Div Biotechnol, Iksan 54596, South Korea
关键词
Nociception; Butein; Inflammation; Tail immersion; Capsaicin; POSTOPERATIVE PAIN; MECHANISMS; RECEPTORS; GLUTAMATE; EDEMA; CELLS; CYCLOOXYGENASE-2; FLAVONOIDS; CYTOKINES; CHANNELS;
D O I
10.1016/j.sjbs.2021.08.006
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: Around 30% world population affected by acute and chronic pain due to inflammation and accidental injuries. Pain is a uncomfortable sensation and it reduce the patients' life quality. Objective: The present exploration focuses to explore the beneficial effects of butein on the different chemical and thermal-provoked nociceptive and inflammatory mice models. Methodology: The nociception was induced to the Swiss mice using different chemical (formalin, acetic acid, glutamate, and capsaicin) and thermal (hot plate and tail immersion) methods. the mice were supplemented with 10, 15, and 20 mg/kg of butein and respective standard drugs like morphine, diclofenac sodium, and dexamethasone. The anti-inflammatory effects of butein was studied using carrageenanprovoked inflammation in mice. Results: The present findings clearly demonstrated that the butein was substantially lessened the different thermal and chemical provoked nociception in mice. The carrageenan-triggered paw edema and inflammatory cell infiltrations were appreciably suppressed by the butein treatment. The TNF-alpha, IL-1 beta, and IL-6 levels in the carrageenan-induced mice were effectively depleted by the butein. Conclusion: Altogether, the present findings evidenced the potent antinociceptive and anti-inflammatory properties of the butein in different nociceptive mice models. (C) 2021 The Author(s). Published by Elsevier B.V. on behalf of King Saud University.
引用
收藏
页码:7090 / 7097
页数:8
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