Abstract

BackgroundCold stress, which may lead to local and systemic injury, is reported to be related to the immune system, especially the complement system. At present, the lack of effective treatment is a critical issue. Amentoflavone (AF), which can inhibit cold stress-induced inflammation in lung by multiple mechanisms, is the main therapeutic ingredient in plants of the genus Selaginella.ResultsIn the current study, we found that cold could induce lung inflammation related to the complement system and its downstream pathways. AF treatment significantly inhibited lung inflammation from cold exposure. We presented evidence that AF can bind to complement component 3 (C3) to regulate inflammation-related pathways involving Lck/Yes novel tyrosine kinase (Lyn), protein kinase B (Akt), nuclear factor-κB (NF-κB) and immune factors. Moreover, 30 mg/kg of AF caused significantly greater improvement than 15 mg/kg in reducing the level of C3 in lung tissue.ConclusionsAF can protect lung tissue from cold exposure. The protective effect may be achieved by inhibition of C3 and negative regulation of the B cell receptor (BCR)/NF-κB signaling pathways and high mobility group box 1 (HMGB1), which ultimately ameliorates the inflammatory response.

Highlights

  • Cold stress, which may lead to local and systemic injury, is reported to be related to the immune system, especially the complement system

  • We have found that damage to lungs, may relate directly to a local inflammatory response induced by cold injury [4]

  • The results suggest that AF pretreatment has a protective effect against lung injury due to cold exposure

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Summary

Introduction

Cold stress, which may lead to local and systemic injury, is reported to be related to the immune system, especially the complement system. Amentoflavone (AF), which can inhibit cold stress-induced inflammation in lung by multiple mechanisms, is the main therapeutic ingredient in plants of the genus Selaginella. A severe and acute period of stress, may lead to local and systemic injury caused by the immune system [1]. There are many hypotheses regarding how cold stress causes injury in target organs. Exposure to cold stress can directly cause hemodynamic changes, resulting in thrombosis, tissue ischemia and reperfusion, and inflammatory injury [3]. Cold-induced target organ damage occurs first in tissues with abundant blood flow. The lungs are directly exposed to cold air, inducing smooth muscle contraction

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