Protective Effects of Atractylodis Rhizoma Extracts on Lung Injury Induced by Particulate Matter 2.5 in Mice

This study investigated the lung-protective effects of Atractylodis Rhizoma extracts (the root of <i>Atractylodes japonica</i> Koidz. ex Kitam), known as AJ extracts, in mitigating subacute pulmonary injuries caused by particulate matter 2.5 (PM<sub>2.5</sub>) exposure in Balb/c mice. AJ was given orally at concentrations of 400, 200, and 100 mg/kg, demonstrating a promising impact by mitigating oxidative stress and inflammation associated with phosphoinositide 3-kinase/protein kinase B (<i>PI3K/Akt</i>) and p38 mitogen-activated protein kinase α (<i>p38 MAPKα</i>) pathways and reducing mucus overproduction. These protective effects were achieved through the downregulation of <i>p38 MAPKα</i> and <i>PI3K/Akt</i> mRNA expressions, enhanced anti-inflammatory and antioxidant activities, and increased mucolytic expectorant effects arbitrated by elevated lung acetylcholine (ACh) and substance P levels, along with decreased mRNA expressions of <i>MUC5AC</i> and <i>MUC5B</i>. Importantly, these outcomes occurred without significant hepatotoxicity. While all AJ dosages provided dose-dependent pulmonary protection, their effects were less pronounced than those of dexamethasone (DEXA) at 0.75 mg/kg. However, AJ uniquely exhibited mucolytic expectorant activities absent in DEXA-treated mice. The results indicate that <i>A. japonica</i> may serve as a potential candidate for creating alternative treatments for respiratory conditions or as an ingredient in functional foods.

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Publication Details

Journal
Antioxidants
Published
2025-01-23
DOI
https://doi.org/10.3390/antiox14020127
Citations
3
Primary Topic
Chronic Obstructive Pulmonary Disease (COPD) Research
Type
article
Field-Weighted Citation Impact
4.56

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article

Protective Effects of Atractylodis Rhizoma Extracts on Lung Injury Induced by Particulate Matter 2.5 in Mice

Sae‐Kwang Ku, Eunjeong Yun, Young-Sam Kwon, Jae‐Suk Choi et al.
3 citations
Antioxidants
Chronic Obstructive Pulmonary Disease (COPD) Research
4.56
article

Protective Effects of Atractylodis Rhizoma Extracts on Lung Injury Induced by Particulate Matter 2.5 in Mice

Sae‐Kwang Ku, Eunjeong Yun, Young-Sam Kwon, Jae‐Suk Choi, Khawaja Muhammad Imran Bashir, Hye Jin Chung, Jeongjun Lee
article en
3 citations

Abstract

This study investigated the lung-protective effects of Atractylodis Rhizoma extracts (the root of <i>Atractylodes japonica</i> Koidz. ex Kitam), known as AJ extracts, in mitigating subacute pulmonary injuries caused by particulate matter 2.5 (PM<sub>2.5</sub>) exposure in Balb/c mice. AJ was given orally at concentrations of 400, 200, and 100 mg/kg, demonstrating a promising impact by mitigating oxidative stress and inflammation associated with phosphoinositide 3-kinase/protein kinase B (<i>PI3K/Akt</i>) and p38 mitogen-activated protein kinase α (<i>p38 MAPKα</i>) pathways and reducing mucus overproduction. These protective effects were achieved through the downregulation of <i>p38 MAPKα</i> and <i>PI3K/Akt</i> mRNA expressions, enhanced anti-inflammatory and antioxidant activities, and increased mucolytic expectorant effects arbitrated by elevated lung acetylcholine (ACh) and substance P levels, along with decreased mRNA expressions of <i>MUC5AC</i> and <i>MUC5B</i>. Importantly, these outcomes occurred without significant hepatotoxicity. While all AJ dosages provided dose-dependent pulmonary protection, their effects were less pronounced than those of dexamethasone (DEXA) at 0.75 mg/kg. However, AJ uniquely exhibited mucolytic expectorant activities absent in DEXA-treated mice. The results indicate that <i>A. japonica</i> may serve as a potential candidate for creating alternative treatments for respiratory conditions or as an ingredient in functional foods.

AntioxidantsVol. 14(2)
Daegu Haany University (KR), Gyeongsang National University (KR), Kyungpook National University (KR)
Gyeongsang National University
Good health and well-being
Openalex Percentile: Top 7%
Chronic Obstructive Pulmonary Disease (COPD) Research
4.56
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