Startseite Ethanolic extract of Achillea wilhelmsii C. Koch improves pulmonary function and inflammation in LPS-induced acute lung injury mice
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Ethanolic extract of Achillea wilhelmsii C. Koch improves pulmonary function and inflammation in LPS-induced acute lung injury mice

  • Niloofar Honari , Parastoo Shaban , Saeed Nasseri und Mehran Hosseini ORCID logo EMAIL logo
Veröffentlicht/Copyright: 6. Mai 2021

Abstract

Objectives

Acute lung injury (ALI) is a life-threatening pulmonary dysfunction associated with severe inflammation. There are still no effective pharmacological therapies for the treatment of ALI. In this concern, several anti-inflammatory agents could be used as add-on therapy to inhibit inflammation. Achillea wilhelmsii (AW) C. Koch is a well-known medicinal plant in the Iranian ethnomedical practices with anti-inflammatory activity. This study was aimed to evaluate the efficacy of ethanolic extract of AW on lipopolysaccharide (LPS)-induced ALI in mice.

Methods

The ALI model was established via the intra-tracheal (i.t.) administration of LPS (2 mg/kg) to male BALB/c mice. The ALI mice were divided into four groups (n=8 each) which intra-peritoneally (i.p.) treated with repeated doses of saline (model), dexamethasone (2 mg/kg), and AW (150–300 mg/kg) 1, 11 and 23 h post LPS administration. Twenty-four hours after the LPS challenge, bronchoalveolar lavage fluid (BALF) and lung tissue were evaluated for inflammatory cell influx, level of tumor necrosis factor-α (TNF-α) and histopathological changes.

Results

The AW (150–300 mg/kg) treated mice showed lower inflammatory cells infiltration in BALF and TNF-α level when compared to the model group. In addition, LPS induced several pathological alterations such as edema, alveolar hemorrhage and inflammatory cell infiltration into the interstitium and alveolar spaces. Treatment with AW significantly reduced LPS-induced pathological injury.

Conclusions

Taken together, the data here indicated that AW may be considered as a promising add-on therapy for ALI.


Corresponding author: Mehran Hosseini, Cellular and Molecular Research Center, Department of Anatomical Sciences, Birjand University of Medical Sciences, Birjand, Iran, E-mail:

Award Identifier / Grant number: 5150

Acknowledgments

We appreciate Ms. Vazifeshenas and Mr. Kabiri (Laboratory technologists, BUMS) for their technical assistance. The authors would like to thank Dr. Zardast for helping us in cell differentiation.

  1. Research funding: Birjand University of Medical Sciences (Grant number: 5150).

  2. Author contributions: All authors have accepted responsibility for the entire content of this manuscript and approved its submission.

  3. Competing interests: The authors have no financial or nonfinancial conflicts of interest to declare.

  4. Informed consent: Not applicable.

  5. Ethical approval: All procedures involving animals were in accordance with the national guides in care and use of Laboratory Animals in Scientific Affairs provided by the Iranian Ministry of Health and Medical Education (2019). The guideline is following 1964 Helsinki declaration and its later amendments or comparable ethical standards. Moreover, the animal experiments were approved by the Birjand University of Medical Sciences Ethics Committee (permit code: IR.BUMS.REC.1398.260).

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Received: 2021-01-30
Accepted: 2021-04-06
Published Online: 2021-05-06

© 2021 Walter de Gruyter GmbH, Berlin/Boston

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