Evidence map›Paper›PMID 42787714›Full record

ArticleIranian journal of basic medical sciences2026

Protective effect of linalool against morphine-induced renal injury: Modulation of oxidative stress and PI3K/AKT/L-FABP signaling pathway.

Shokouh Shayanpour, Maryam Radan, Khojasteh Hoseinynejad, Seyedeh Parisa Navabi, Mohsen Khanlari Piraliloo, Parastoo Moradi Choghakabodi

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Article in Iranian journal of basic medical sciences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Shokouh ShayanpourCellular and Molecular Research Center, Medical Basic Sciences Research Institute, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran.
Maryam RadanCellular and Molecular Research Center, Medical Basic Sciences Research Institute, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran.
Khojasteh HoseinynejadCellular and Molecular Research Center, Medical Basic Sciences Research Institute, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran.
Seyedeh Parisa NavabiDepartment of Physiology, Persian Gulf Physiology Research Center, Medical Basic Sciences Research Institute, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran.
Mohsen Khanlari PiralilooDepartment of Physiology, Persian Gulf Physiology Research Center, Medical Basic Sciences Research Institute, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran.
Parastoo Moradi ChoghakabodiSchool of Medicine, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objectives: Opioid misuse and prolonged therapeutic use are increasingly linked to systemic toxicities, including renal dysfunction. Morphine has been shown to induce oxidative stress and disrupt intracellular signaling pathways implicated in kidney injury. Linalool, a naturally occurring monoterpene with antioxidant and anti-inflammatory properties, may protect against drug-induced nephrotoxicity. This study investigated the protective effects of linalool against morphine-induced renal injury in rats, focusing on oxidative stress parameters and modulation of the PI3K/AKT/L-FABP signaling pathway. Materials and Methods: Thirty-two male Wistar rats were randomly allocated into four groups (n=8/group): Control, Morphine (10 mg/kg, SC), Linalool (50 mg/kg, IP), and Morphine + Linalool. Treatments were administered for three consecutive days using a conditioned place preference protocol to model morphine exposure. Renal function markers, oxidative stress parameters (MDA, SOD, CAT), histopathological alterations, and renal expression of AKT, PI3K, and L-FABP proteins were evaluated. Results: Morphine administration significantly elevated serum creatinine, urinary injury markers, and lipid peroxidation (MDA), while decreasing antioxidant enzyme activities (SOD and CAT). Morphine also down-regulated AKT expression and PI3K, and up-regulated FABP in renal tissue. Co-treatment with linalool significantly improved biochemical parameters, attenuated histopathological damage, reduced oxidative stress, suppressed FABP overexpression, and restored AKT and PI3K expression. Conclusion: Linalool exerts renoprotective effects against morphine-induced injury by reducing oxidative stress and modulating PI3K/AKT/L-FABP signaling. These findings suggest that linalool has therapeutic potential for preventing opioid-associated renal dysfunction.

Indexed as

Acute kidney injuryL-FABPLinaloolMorphineOxidative stressPI3K/AKT

Identifiers

PMID42787714
PMCPMC13602874

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.