# Protective Effect of Protaetia brevitarsis Larvae Extract on Alcoholic Liver Disease in Mice

**Authors:** Sueun Lee, Young Hye Seo, Yun‐Soo Seo, Hyeon‐Hwa Nam, Jun Lee, Joong‐Sun Kim, Ji Hye Lee

PMC · DOI: 10.1002/fsn3.71616 · Food Science & Nutrition · 2026-03-06

## TL;DR

A study found that a water extract from Protaetia brevitarsis larvae may protect mice from alcohol-induced liver damage by reducing inflammation and oxidative stress.

## Contribution

This study is the first to investigate the hepatoprotective effects of Protaetia brevitarsis larvae extract in an alcohol-induced liver disease model.

## Key findings

- PBLE reduced hepatic lipid accumulation and liver injury in mice.
- PBLE modulated alcohol metabolism-related enzymes and reduced oxidative stress and inflammation.
- Six bioactive components were identified in PBLE using ultra-high-performance liquid chromatography.

## Abstract

Protaetia brevitarsis larvae (PBLs) are edible insects traditionally used in oriental medicine to manage various liver diseases, including hepatitis, liver cirrhosis, and hepatic cancer. However, the effects of PBL water extract (PBLE) on alcohol‐induced liver disease remain unexplored. This study investigated the hepatoprotective effects of PBLE using a chronic‐plus‐single‐binge ethanol feeding model. PBLE (100 or 200 mg/kg/day) was orally administered in combination with an ethanol diet. Mice were euthanised 9 h post‐binge, and serum and liver tissues were collected for histological, biochemical, and molecular analyses. Six components (adenine, adenosine, hypoxanthine, inosine, benzoic acid, and uridine) were isolated from PBLE by ultra‐high‐performance liquid chromatography. PBLE treatment alleviated hepatic morphological changes, such as lipid droplet accumulation and hepatocytic ballooning, and reduced the elevated liver enzymes and triglyceride levels in the serum. Moreover, PBLE attenuated against the altered expression of alcohol metabolism‐related enzymes (alcohol dehydrogenase, aldehyde dehydrogenase, and cytochrome P450 2E1) in the liver. PBLE also exhibited anti‐inflammatory and antioxidant effects by normalizing the hepatic expression of p65, inducible nitric oxide synthase, cyclooxygenase‐2, interleukin‐1 beta, and tumor necrosis factor alpha, as well as nuclear factor erythroid 2‐related factor 2, haem oxygenase 1, glutathione peroxidase 3, superoxide dismutase, and catalase. In conclusion, PBLE may exert therapeutic effects on alcohol‐induced liver injury by improving alcohol metabolism and reducing oxidative stress and inflammation. These findings indicate that the edible beetle PBLs may serve as a hepatoprotective functional food ingredient.

This study evaluated the hepatoprotective effects of Protaetia brevitarsis larvae water extract (PBLE) in a chronic‐plus‐binge ethanol mouse model. PBLE attenuated hepatic lipid accumulation and liver injury by modulating alcohol metabolism‐related enzymes and reducing oxidative stress and inflammation. These findings suggest that PBLE may serve as a potential functional food ingredient for alcohol‐induced liver injury.

## Linked entities

- **Proteins:** ATA1 (TAPETUM 1), RELA (RELA proto-oncogene, NF-kB subunit), GPX3 (glutathione peroxidase 3), Cat (Catalase)
- **Chemicals:** adenine (PubChem CID 190), adenosine (PubChem CID 60961), hypoxanthine (PubChem CID 135398638), inosine (PubChem CID 135398641), benzoic acid (PubChem CID 243), uridine (PubChem CID 6029)
- **Diseases:** alcoholic liver disease (MONDO:0043693), hepatitis (MONDO:0002251), hepatic cancer (MONDO:0002691)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** Cxcl2 (C-X-C motif chemokine ligand 2) [NCBI Gene 20310] {aka CINC-2a, GROb, Gro2, MIP-2, MIP-2a, Mgsa-b}, Nos2 (nitric oxide synthase 2, inducible) [NCBI Gene 18126] {aka MAC-NOS, NOS-II, Nos-2, Nos2a, i-NOS, iNOS}, Aldh2 (aldehyde dehydrogenase 2, mitochondrial) [NCBI Gene 11669] {aka AHD-M1, ALDH-E2, ALDHI, Ahd-5, Ahd5}, Tnf (tumor necrosis factor) [NCBI Gene 21926] {aka DIF, TNF-a, TNF-alpha, TNFSF2, TNFalpha, Tnfa}, Cyp2e1 (cytochrome P450, family 2, subfamily e, polypeptide 1) [NCBI Gene 13106] {aka CYPIIE1, Cyp2e}, Stk4 (serine/threonine kinase 4) [NCBI Gene 58231] {aka Kas-2, Mst1, Ysk3}, Acsl4 (acyl-CoA synthetase long-chain family member 4) [NCBI Gene 50790] {aka 9430020A05Rik, ACS4, Facl4, Lacs4}, Slc17a5 (solute carrier family 17 (anion/sugar transporter), member 5) [NCBI Gene 235504] {aka 4631416G20Rik, 4732491M05, AST, ISSD, NSD, SD}, Atf4 (activating transcription factor 4) [NCBI Gene 11911] {aka Atf-4, C/ATF, CREB-2, CREB2, TAXREB67}, Rela (Rela proto-oncogene, NFKB subunit) [NCBI Gene 19697] {aka p65, p65 NF-kappa B, p65 NFkB}, Ptgs2 (prostaglandin-endoperoxide synthase 2) [NCBI Gene 19225] {aka COX2, Cox-2, PES-2, PGHS-2, PHS II, PHS-2}, Adh1 (alcohol dehydrogenase 1 (class I)) [NCBI Gene 11522] {aka ADH-A2, ADH-AA, Adh-1, Adh-1-t, Adh-1e, Adh-1t}, Akr1a1 (aldo-keto reductase family 1, member A1) [NCBI Gene 58810] {aka 2610201A18Rik, Akr1a4}, Gpt (glutamic pyruvic transaminase, soluble) [NCBI Gene 76282] {aka 1300007J06Rik, 2310022B03Rik, ALT, ALT1, Gpt-1, Gpt1}, Sod1 (superoxide dismutase 1, soluble) [NCBI Gene 20655] {aka B430204E11Rik, Cu/Zn-SOD, CuZnSOD, Ipo-1, Ipo1, SODC}, Hmox1 (heme oxygenase 1) [NCBI Gene 15368] {aka D8Wsu38e, HO-1, HO1, Hemox, Hmox, Hsp32}, Aldh3a1 (aldehyde dehydrogenase family 3, subfamily A1) [NCBI Gene 11670] {aka Ahd-4, Ahd4, Aldh, Aldh3}, Cat (catalase) [NCBI Gene 12359] {aka 2210418N07, Cas-1, Cas1, Cs-1}, Nfe2l2 (nuclear factor, erythroid derived 2, like 2) [NCBI Gene 18024] {aka Nrf2}, Gpx3 (glutathione peroxidase 3) [NCBI Gene 14778] {aka EGPx, GPx, GSHPx-3, GSHPx-P}, Sod3 (superoxide dismutase 3, extracellular) [NCBI Gene 20657] {aka EC-SOD}, Il1b (interleukin 1 beta) [NCBI Gene 16176] {aka IL-1beta, Il-1b}, Il6 (interleukin 6) [NCBI Gene 16193] {aka Il-6}, Actb (actin, beta) [NCBI Gene 11461] {aka Actx, E430023M04Rik, beta-actin}, H3c7 (H3 clustered histone 7) [NCBI Gene 260423] {aka H3.2-221, H3c13, H3c14, H3c15, H3c2, H3c3}, Sod2 (superoxide dismutase 2, mitochondrial) [NCBI Gene 20656] {aka MnSOD, Sod-2}, COX2 (cytochrome c oxidase subunit II) [NCBI Gene 17709]
- **Diseases:** oedema (MESH:C536897), toxicity (MESH:D064420), excessive (MESH:D006970), deaths (MESH:D003643), hepatocellular carcinoma (MESH:D006528), hepatic lipid (MESH:D011017), hepatic cancer (MESH:D008113), ALD (MESH:D008108), kidney impairment (MESH:D007674), Hepatic Injury (MESH:D056486), dementia (MESH:D003704), UPLC (MESH:D008228), liver injury (MESH:D017093), liver cirrhosis (MESH:D008103), Inflammatory (MESH:D007249), hepatic disorders (MESH:D008107), cirrhosis (MESH:D005355), alcohol dependence (MESH:D000437), fat (MESH:D004620), Liver steatosis (MESH:D005234), jaundice (MESH:D007565)
- **Chemicals:** malondialdehyde (MESH:D008315), hydrogen peroxide (MESH:D006861), Chemical (-), superoxide (MESH:D013481), maltose (MESH:D008320), H&amp;E (MESH:D006371), Tween 20 (MESH:D011136), polyvinylidene fluoride (MESH:C024865), Alcohol (MESH:D000438), hydrogen (MESH:D006859), acetaldehyde (MESH:D000079), N-acetylcysteine (MESH:D000111), formalin (MESH:D005557), reactive oxygen species (MESH:D017382), glutathione (MESH:D005978), astaxanthin (MESH:C005948), lipid (MESH:D008055), purine (MESH:C030985), Benzoic acid (MESH:D019817), xylazine (MESH:D014991), acetonitrile (MESH:C032159), TG (MESH:D014280), polyacrylamide (MESH:C016679), inosine (MESH:D007288), paraffin (MESH:D010232), adenosine (MESH:D000241), saline (MESH:D012965), PV (MESH:D010404), formic acid (MESH:C030544), phosphate (MESH:D010710), dioxygen (MESH:D010100), uridine (MESH:D014529), hypoxanthine (MESH:D019271), colchicine (MESH:D003078), acetic acid (MESH:D019342), sodium dodecyl sulphate (MESH:D012967), adenine (MESH:D000225), EtOH (MESH:D000431), nitric oxide (MESH:D009569), pyrimidine (MESH:C030986), B (MESH:D001895), water (MESH:D014867), pentoxifylline (MESH:D010431), ADH (MESH:C010011), S-adenosyl methionine (MESH:D012436), alfaxalone (MESH:C006477)
- **Species:** Protaetia brevitarsis (species) [taxon 348688], Homo sapiens (human, species) [taxon 9606], Protaetia (genus) [taxon 348687], Mus musculus (house mouse, species) [taxon 10090]

## Full text

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## References

66 references — full list in the complete paper: https://tomesphere.com/paper/PMC12966768/full.md

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Source: https://tomesphere.com/paper/PMC12966768