# Non‐Pulmonary Mechanisms of Action of Ambroxol in In Vivo Experimental Models: a Systematic Review

**Authors:** Michelline Joana Tenório Albuquerque Madruga Mesquita, Anne Caroline Silva Nogueira da Cruz, Rafael de Abreu Lima, Joana Tenório‐Meireles, Arney José Nogueira Farias, Isabela Nogueira Santos, Gustavo Frota, Taciana Gabrielle Pinheiro de Moura Carvalho, Rafael Antônio Freire Carvalho, Jorge Antônio Meireles‐Teixeira, Tereza Prazeres, Rafael Cardoso Carvalho, Maria do Socorro de Sousa Cartágenes, João Batista Santos Garcia

PMC · DOI: 10.1111/fcp.70077 · Fundamental & Clinical Pharmacology · 2026-03-13

## TL;DR

This paper reviews how ambroxol, a drug mainly used for respiratory issues, may also help with non-lung conditions like inflammation and pain in animal models.

## Contribution

The study systematically reviews non-pulmonary mechanisms of ambroxol in experimental models, highlighting its anti-inflammatory and antioxidant potential.

## Key findings

- Ambroxol showed antioxidant effects by reducing free radicals and boosting SOD, CAT, and GSH activity.
- It reduced pro-inflammatory cytokines like TNF-α and IL-1β in various disease models.
- Ambroxol alleviated neuropathic pain by inhibiting sodium channels and reducing oxidative stress.

## Abstract

Repositioning offers a cost‐effective approach to discovering new therapeutic applications for existing medications. Ambroxol, primarily used as a mucolytic for respiratory diseases, has demonstrated anti‐inflammatory, analgesic, and antioxidant properties, suggesting potential benefits in non‐pulmonary conditions. This study conducted a systematic review to evaluate the efficacy of ambroxol in experimental disease models unrelated to the respiratory system.

Following registration in the Open Science Framework and adherence to the PICO strategy for formulating the guiding question, searches were performed in PUBMED/MEDLINE, EMBASE, and SCOPUS using the keywords: (Ambroxol) AND (Anti‐Inflammatory Agents OR Analgesics OR Antioxidants) AND (Animals OR in vivo). The SYRCLE tool assessed methodological quality. Among 353 identified records, eight articles met eligibility criteria.

These studies investigated ambroxol's effects in models of gastric lesions, neuropathic pain, psoriasis‐like skin inflammation, hemorrhagic cystitis, and ischemia/reperfusion injuries in the liver and kidneys. Ambroxol doses ranged from 5 to 1000 mg/kg, predominantly administered orally. Its antioxidant properties were demonstrated by reducing free radicals and increasing enzymatic activity (SOD, CAT, GSH). Anti‐inflammatory effects included a decrease in pro‐inflammatory cytokines (TNF‐α, IL‐1β) and histological improvements. Antinociceptive action was observed through inhibition of voltage‐gated sodium channels and reduction of oxidative stress, alleviating neuropathic pain.

Despite ambroxol's widespread clinical use, limited research has explored its non‐respiratory applications. Existing studies suggest its promising therapeutic potential, reinforcing the need for further investigation into its role as an alternative treatment for various inflammatory and oxidative stress–related conditions beyond pulmonary diseases.

## Linked entities

- **Proteins:** SOD1 (superoxide dismutase 1), CAT (catalase), LOC23687505 (pyrimidodiazepine synthase), TNF (tumor necrosis factor), IL1B (interleukin 1 beta)
- **Chemicals:** ambroxol (PubChem CID 2132)
- **Diseases:** hemorrhagic cystitis (MONDO:0000496)

## Full-text entities

- **Genes:** CAT (catalase) [NCBI Gene 847], IL1B (interleukin 1 beta) [NCBI Gene 3553] {aka IL-1, IL1-BETA, IL1F2, IL1beta}, Il17a (interleukin 17A) [NCBI Gene 301289] {aka CTLA-8, IL-17, IL-17A, Il17}, Mpo (myeloperoxidase) [NCBI Gene 303413], TLR8 (toll like receptor 8) [NCBI Gene 51311] {aka CD288, IMD98, TLR-8, hTLR8}, Cat (catalase) [NCBI Gene 24248] {aka CS1, Cas1, Cat01, Catl, Cs-1}, Got2 (glutamic-oxaloacetic transaminase 2) [NCBI Gene 25721] {aka ASPATA, mAAT}, Tnf (tumor necrosis factor) [NCBI Gene 24835] {aka RATTNF, TNF-alpha, Tnfa}, Tgfb1 (transforming growth factor, beta 1) [NCBI Gene 59086] {aka Tgfb}, SOD1 (superoxide dismutase 1) [NCBI Gene 6647] {aka ALS, ALS1, HEL-S-44, IPOA, SOD, STAHP}, Il22 (interleukin 22) [NCBI Gene 500836] {aka If2b1, RGD1561292}, Pdlim3 (PDZ and LIM domain 3) [NCBI Gene 114108] {aka Actn2lp, Alp}, TLR7 (toll like receptor 7) [NCBI Gene 51284] {aka IMD74, SLEB17, TLR7-like}, Il10 (interleukin 10) [NCBI Gene 25325] {aka IL10X, If2a}, Tnf (tumor necrosis factor) [NCBI Gene 21926] {aka DIF, TNF-a, TNF-alpha, TNFSF2, TNFalpha, Tnfa}, tumor necrosis factor [NCBI Gene 103694380], Il6 (interleukin 6) [NCBI Gene 24498] {aka ILg6, Ifnb2}, Il1b (interleukin 1 beta) [NCBI Gene 24494] {aka IL-1F2}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}
- **Diseases:** non-respiratory diseases (MESH:D012140), SYRCLE (MESH:D007757), spinal cord injury (MESH:D013119), liver injury (MESH:D017093), chronic bronchitis (MESH:D029481), pain (MESH:D010146), bladder injury (MESH:D001745), heat hypersensitivity (MESH:D004342), skin lesions (MESH:D012871), neurodegenerative diseases (MESH:D019636), Inflammation (MESH:D007249), psoriasis (MESH:D011565), reperfusion injuries (MESH:D015427), genital warts (MESH:D003218), neuropathy (MESH:D009422), ischemic injuries (MESH:D017202), ACH (MESH:D000130), pulmonary diseases (MESH:D008171), epidermal hyperplasia (MESH:D006965), hepatic ischemia (MESH:D007511), edema (MESH:D004487), ulcers (MESH:D014456), injury (MESH:D014947), hepatic injury (MESH:D056486), hemorrhage (MESH:D006470), neuropathic pain (MESH:D009437), OSF (MESH:D005597), allodynia (MESH:D006930), cancerous skin abnormalities (MESH:D012878), acute and chronic pain (MESH:D059787), tissue damage (MESH:D017695), Antral (MESH:D020252), renal injury (MESH:D007674), gastric injury (MESH:D013272), analgesia (MESH:D000699), acute lung injury (MESH:D055371)
- **Chemicals:** oxaliplatin (MESH:D000077150), LPS (MESH:D008070), IMQ (MESH:D000077271), CYP (MESH:D003520), lipid (MESH:D008055), ABX (MESH:D000551), free radicals (MESH:D005609), bromhexine (MESH:D001964), nitrite (MESH:D009573), AED (-), pregabalin (MESH:D000069583), creatinine (MESH:D003404), indomethacin (MESH:D007213), sodium (MESH:D012964), leukotrienes (MESH:D015289), superoxide anion (MESH:D013481), GSH (MESH:D005978), acetone (MESH:D000096), MDA (MESH:D008315), TBARS (MESH:D017392), histamine (MESH:D006632)
- **Species:** Homo sapiens (human, species) [taxon 9606], Mus musculus (house mouse, species) [taxon 10090], Human papillomavirus (species) [taxon 10566], Rattus norvegicus (brown rat, species) [taxon 10116], Justicia adhatoda (species) [taxon 141317]

## Full text

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## References

28 references — full list in the complete paper: https://tomesphere.com/paper/PMC12987714/full.md

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Source: https://tomesphere.com/paper/PMC12987714