Huperzine A versus epicatechin: a comparative study of their potential protective effect on lipopolysaccharide-induced lung injury in mice

Authors

  • Zeena Thamir Tariq
  • Ahmed R. Abu-Raghif
  • Abdulla K. Raheem
  • Hayder Ridha-Salman
  • Alaa Hamza Abbas
  • Qassim A. Zigam
  • Weaam J. Abbas
  • Maytham Ahmed AbdulAemah
  • Hasanain A. M. Abbas
  • Ali Jihad Hemid Al-Athari
  • Elaf Mahmood Shihab
  • Salim K. Hajwal
  • Ahmed Abbas Al-Khafaji
  • Mahdi Hamzah Al-Taee

DOI:

https://doi.org/10.60988/p.v37i2S.244

Keywords:

huperzine A; epicatechin; methylprednisolone; lipopolysaccharide; cytokine storm

Abstract

A cytokine storm is a severe and potentially fatal condition resulting from an excessive immune response. Epicatechin and huperzine A have demonstrated anti-inflammatory and antioxidant properties, suggesting their potential utility in mitigating tissue damage and cytokine storm severity. This study aimed to compare the protective effects of huperzine A and epicatechin in a cytokine storm-like murine model. Sixty male Swiss albino mice were randomly allocated into six groups. Except for the control group, all animals received a single intraperitoneal injection of lipopolysaccharide (LPS; 5 mg/kg) in order to induce a cytokine storm. The induction group received LPS without further intervention. The remaining groups were pre-treated for three consecutive days prior to LPS administration as follows: vehicle group (1% dimethyl sulfoxide), methylprednisolone group (50 mg/kg/day methylprednisolone), huperzine A group (0.2 mg/kg/day huperzine A), and epicatechin group (25 mg/kg/day epicatechin). The histological analysis of lung tissues and the quantification of serum cytokines – interleukin-1 beta (IL-1β), interleukin-6 (IL-6), and tumor necrosis factor-alpha (TNF-α) – revealed that all pre-treated groups exhibited significant anti-inflammatory effects. Notably, epicatechin conferred a more pronounced protective effect than either methylprednisolone or huperzine A, as evidenced by reduced pulmonary histopathological alterations and lower serum cytokine concentrations. In conclusion, both huperzine A and epicatechin demonstrated protective efficacy against the LPS-induced cytokine storm, with epicatechin showing superior performance in attenuating systemic inflammation and lung injury.

Author Biographies

Zeena Thamir Tariq

Antimicrobial Resistance Sector, Public Health Directorate, Ministry of Health, Baghdad, Iraq

Ahmed R. Abu-Raghif

Department of Pharmacology, College of Medicine, Al-Nahrain University, Baghdad, Iraq

Abdulla K. Raheem

Department of Pharmacology, College of Pharmacy, Al-Mustaqbal University, Hillah, Iraq

Hayder Ridha-Salman

Department of Pharmacology, College of Pharmacy, Al-Mustaqbal University, Hillah, Iraq

Alaa Hamza Abbas

Department of Pharmacology, College of Pharmacy, Al-Mustaqbal University, Hillah, Iraq

Qassim A. Zigam

Department of Pharmacology, College of Pharmacy, Al-Mustaqbal University, Hillah, Iraq

Weaam J. Abbas

Department of Pharmacology, College of Pharmacy, Al-Mustaqbal University, Hillah, Iraq

Maytham Ahmed AbdulAemah

Department of Pharmacology, College of Pharmacy, Al-Mustaqbal University, Hillah, Iraq

Hasanain A. M. Abbas

Department of Pharmacology, College of Pharmacy, Al-Mustaqbal University, Hillah, Iraq

Ali Jihad Hemid Al-Athari

Department of Pharmacology, College of Pharmacy, Al-Mustaqbal University, Hillah, Iraq

Elaf Mahmood Shihab

Department of Pharmacology and Toxicology, College of Pharmacy, Al-Esraa University, Baghdad, Iraq

Salim K. Hajwal

Department of Nursing, College of Nursing, Al-Mustaqbal University, Hillah, Iraq

Ahmed Abbas Al-Khafaji

Department of Pharmacology, College of Pharmacy, Al-Mustaqbal University, Hillah, Iraq

Mahdi Hamzah Al-Taee

Department of Nursing, College of Nursing, Al-Mustaqbal University, Hillah, Iraq

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Published

10-10-2025

How to Cite

[1]
Tariq, Z.T. et al. 2025. Huperzine A versus epicatechin: a comparative study of their potential protective effect on lipopolysaccharide-induced lung injury in mice. Pharmakeftiki . 37, 2S (Oct. 2025). DOI:https://doi.org/10.60988/p.v37i2S.244.