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Protective Effects of Apamin on Acetaminophen-Induced Hepatotoxicity in Mice

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Publisher MDPI
Specialty Molecular Biology
Date 2023 May 26
PMID 37232748
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Abstract

Acetaminophen (APAP) overdose can cause severe liver damage, but therapeutic options are limited. Apamin is a natural peptide present in bee venom and has antioxidant and anti-inflammatory properties. Accumulating evidence suggests that apamin has favorable actions in rodent models of inflammatory disorders. Here, we examined the effect of apamin on APAP-evoked hepatotoxicity. Intraperitoneal administration of apamin (0.1 mg/kg) alleviated histological abnormalities and reduced serum levels of liver enzymes in mice injected with APAP. Apamin inhibited oxidative stress through an increase in the amount of glutathione and activation of the antioxidant system. Apamin also attenuated apoptosis with inhibition of caspase-3 activation. Moreover, apamin reduced serum and hepatic levels of cytokines in APAP-injected mice. These effects were accompanied by suppression of NF-κB activation. Furthermore, apamin inhibited chemokine expression and inflammatory cell infiltration. Our results suggest that apamin dampens APAP-evoked hepatotoxicity through inhibiting oxidative stress, apoptosis, and inflammation.

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References
1.
Mossanen J, Krenkel O, Ergen C, Govaere O, Liepelt A, Puengel T . Chemokine (C-C motif) receptor 2-positive monocytes aggravate the early phase of acetaminophen-induced acute liver injury. Hepatology. 2016; 64(5):1667-1682. DOI: 10.1002/hep.28682. View

2.
Matsumoto K, Kawanaka H, Hori M, Kusamori K, Utsumi D, Tsukahara T . Role of transient receptor potential melastatin 2 in surgical inflammation and dysmotility in a mouse model of postoperative ileus. Am J Physiol Gastrointest Liver Physiol. 2018; 315(1):G104-G116. DOI: 10.1152/ajpgi.00305.2017. View

3.
Kim J, Leem J, Park K . Antioxidative, Antiapoptotic, and Anti-Inflammatory Effects of Apamin in a Murine Model of Lipopolysaccharide-Induced Acute Kidney Injury. Molecules. 2020; 25(23). PMC: 7731169. DOI: 10.3390/molecules25235717. View

4.
Liu A, Tanaka N, Sun L, Guo B, Kim J, Krausz K . Saikosaponin d protects against acetaminophen-induced hepatotoxicity by inhibiting NF-κB and STAT3 signaling. Chem Biol Interact. 2014; 223:80-6. PMC: 4376644. DOI: 10.1016/j.cbi.2014.09.012. View

5.
Yan M, Huo Y, Yin S, Hu H . Mechanisms of acetaminophen-induced liver injury and its implications for therapeutic interventions. Redox Biol. 2018; 17:274-283. PMC: 6006912. DOI: 10.1016/j.redox.2018.04.019. View