# The potential role of mesenchymal stem cells enhanced with melatonin in renal damage induced experimentally by cecal ligation and puncture in rats

**Authors:** Amina F. Hussein, Manal F. El-Khadragy, Rasha S. Elbeltagy, Ahmed E. Abdel Moneim, Mohga S. Abdalla

PMC · DOI: 10.3389/fimmu.2026.1684692 · 2026-02-20

## TL;DR

Melatonin-preconditioned stem cells show better kidney protection in septic rats compared to stem cells alone.

## Contribution

Melatonin preconditioning significantly enhances mesenchymal stem cell efficacy in treating sepsis-induced kidney injury.

## Key findings

- MSCs+MEL reduced inflammation and oxidative stress more effectively than MSCs alone.
- MSCs+MEL improved kidney function and histology in a rat model of septic AKI.
- Melatonin preconditioning enhanced MSC survival and therapeutic impact.

## Abstract

Sepsis-induced acute kidney injury (AKI) carries high mortality, and treatment options beyond supportive care are limited. Mesenchymal stem cells (MSCs) offer therapeutic potential due to their paracrine properties but are limited by poor survival and engraftment post-transplantation. Preconditioning with melatonin (MEL) may enhance MSC efficacy. This study aimed to compare the renoprotective effects of MSCs alone versus melatonin-preconditioned MSCs (MSCs+MEL) in a rat model of septic AKI.

Polymicrobial sepsis was induced in male Wistar rats via cecal ligation and puncture (CLP). Three hours post-CLP, animals received an intraperitoneal injection of either MSCs (1 × 10^6), MSCs+MEL, or vehicle. Renal function, oxidative/antioxidant markers, inflammatory cytokines (IL-1β, IL-6, TNF-α, NF-κB), apoptosis, and histopathology were assessed.

CLP-induced sepsis resulted in significant AKI, evidenced by elevated inflammatory and apoptotic markers, oxidative stress, and histopathological damage. Both treatment groups showed improved kidney function and histology compared to untreated septic controls. However, the MSCs+MEL combination was significantly more effective. It superiorly reduced the expression of IL-1β, IL-6, TNF-α, NF-κB, attenuated oxidative stress and apoptosis, enhanced antioxidant defenses, and resulted in more pronounced histological improvement, as confirmed by immunohistochemistry.

Preconditioning with melatonin synergistically enhances the therapeutic efficacy of MSCs in septic AKI. The MSCs+MEL combination exerts superior renoprotection by more robustly mitigating inflammation, oxidative stress, and apoptosis while promoting tissue repair.

## Linked entities

- **Proteins:** IL1B (interleukin 1 beta), IL6 (interleukin 6), TNF (tumor necrosis factor), NFKB1 (nuclear factor kappa B subunit 1)
- **Chemicals:** melatonin (PubChem CID 896)
- **Diseases:** acute kidney injury (MONDO:0002492)
- **Species:** Rattus norvegicus (taxon 10116), Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** Cd14 (CD14 molecule) [NCBI Gene 60350], Il6 (interleukin 6) [NCBI Gene 24498] {aka ILg6, Ifnb2}, Mt2 (metallothionein 2) [NCBI Gene 689415] {aka MT-2, MT-II, Mt2A}, glyceraldehyde 3-phosphate dehydrogenase [NCBI Gene 108351137], Bax (BCL2 associated X, apoptosis regulator) [NCBI Gene 24887], Sod1 (superoxide dismutase 1) [NCBI Gene 24786] {aka CuZnSOD}, Bik (BCL2-interacting killer) [NCBI Gene 114496] {aka Biklk, Blk}, Il6 (interleukin 6) [NCBI Gene 16193] {aka Il-6}, Bid (BH3 interacting domain death agonist) [NCBI Gene 64625], Bcl2l2 (Bcl2-like 2) [NCBI Gene 60434] {aka BCL-W, BCL-WEL, BCL-WS, Bclw}, Nfkbia (NFKB inhibitor alpha) [NCBI Gene 25493] {aka RL/IF-1}, Tgfb1 (transforming growth factor, beta 1) [NCBI Gene 59086] {aka Tgfb}, Tnfaip6 (TNF alpha induced protein 6) [NCBI Gene 84397] {aka Tnfip6}, G6pd (glucose-6-phosphate dehydrogenase) [NCBI Gene 24377] {aka G6pdx}, NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}, Il10 (interleukin 10) [NCBI Gene 25325] {aka IL10X, If2a}, Syt1 (synaptotagmin 1) [NCBI Gene 25716] {aka P65}, Fcgr1a (Fc gamma receptor 1A) [NCBI Gene 295279] {aka FcgammaRI, Fcgr1, Fcgr1b}, Gsr (glutathione-disulfide reductase) [NCBI Gene 116686], COX2 (cytochrome c oxidase subunit II) [NCBI Gene 4513] {aka COII, MTCO2}, Mt1a (metallothionein 1a) [NCBI Gene 24567] {aka Mt, Mt1}, Cat (catalase) [NCBI Gene 24248] {aka CS1, Cas1, Cat01, Catl, Cs-1}, p53-ps (Wistar clone pR53P1 p53 pseudogene) [NCBI Gene 301300], Fcgr2b (Fc gamma receptor 2B) [NCBI Gene 289211] {aka CD32, FCRII, FcgammaRIIB2, Fcgr2}, IL1B (interleukin 1 beta) [NCBI Gene 3553] {aka IL-1, IL1-BETA, IL1F2, IL1beta}, Nos2 (nitric oxide synthase 2) [NCBI Gene 24599] {aka Nos2a, iNos}, Gapdh (glyceraldehyde-3-phosphate dehydrogenase) [NCBI Gene 24383] {aka BARS-38, Gapd}, Nfkb1 (nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105) [NCBI Gene 18033] {aka NF-KB1, NF-kappaB, NF-kappaB1, p105, p50, p50/p105}, Hmox1 (heme oxygenase 1) [NCBI Gene 24451] {aka HEOXG, Heox, Hmox, Ho-1, Ho1, hsp32}, Crp (C-reactive protein) [NCBI Gene 25419] {aka Aa1249, Ab1-341, Ab2-196, Ac1-114, Ac1262, Ac2-069}, Sirt3 (sirtuin 3) [NCBI Gene 293615], Tnf (tumor necrosis factor) [NCBI Gene 24835] {aka RATTNF, TNF-alpha, Tnfa}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, Bak1 (BCL2-antagonist/killer 1) [NCBI Gene 116502] {aka Bak}, Mpo (myeloperoxidase) [NCBI Gene 303413], Il1b (interleukin 1 beta) [NCBI Gene 24494] {aka IL-1F2}, Casp3 (caspase 3) [NCBI Gene 25402] {aka CPP32-beta, Lice, Yama}, Bcl2 (BCL2, apoptosis regulator) [NCBI Gene 24224] {aka Bcl-2}, Calm1 (calmodulin 1) [NCBI Gene 24242] {aka CaMI, Calm, Cam1}, Cxcl15 (C-X-C motif chemokine ligand 15) [NCBI Gene 20309] {aka Il8, Scyb15, lungkine, weche}, Mapk9 (mitogen-activated protein kinase 9) [NCBI Gene 50658] {aka SAPK}, Nos1 (nitric oxide synthase 1) [NCBI Gene 24598] {aka bNOS}, Havcr1 (hepatitis A virus cellular receptor 1) [NCBI Gene 286934] {aka KIM-1, Kim1}, Pink1 (PTEN induced kinase 1) [NCBI Gene 298575], Ptgs2 (prostaglandin-endoperoxide synthase 2) [NCBI Gene 29527] {aka COX-2, Cox2, PGHS-2, PHS II, Pghs2}, Prkaa2 (protein kinase AMP-activated catalytic subunit alpha 2) [NCBI Gene 78975] {aka Ampk, Ampka2}, Bcl2l11 (Bcl2-like 11) [NCBI Gene 64547] {aka Bim, BimL, Bod}, Blk (BLK proto-oncogene, Src family tyrosine kinase) [NCBI Gene 364403], Bcl10 (BCL10, immune signaling adaptor) [NCBI Gene 83477], IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, Bcl2l1 (Bcl2-like 1) [NCBI Gene 24888] {aka Bcl-xl, Bcl2l, Bclx, bcl-X}, Tlr4 (toll-like receptor 4) [NCBI Gene 29260], Akt1 (AKT serine/threonine kinase 1) [NCBI Gene 24185] {aka Akt}
- **Diseases:** hyperactivity (MESH:D006948), renal apoptosis (MESH:D006030), vacuolar degeneration (MESH:C536522), multiple organ failure (MESH:D009102), Ed (MESH:C564542), pulmonary inflammation (MESH:D011014), AKI (MESH:D058186), GD (MESH:D005776), tumor (MESH:D009369), hepatic necrosis (MESH:D047508), morbidities (OMIM:614963), acute tubular necrosis (MESH:D007683), Oliguria (MESH:D009846), lung injury (MESH:D055370), edema (MESH:D004487), critically ill (MESH:D016638), renal fibrosis (MESH:D005355), Inflammation (MESH:D007249), injury (MESH:D014947), mitochondrial damage (MESH:D028361), septic (MESH:D001170), septic shock (MESH:D012772), dislocation (MESH:D004204), Sepsis (MESH:D018805), CLP (MESH:D002429), tissue damage (MESH:D017695), intravascular coagulation (MESH:D004211), damaged kidney (MESH:D007674), and organ damage (MESH:D000092124), cytokine storm (MESH:D000080424), liver, kidney, heart, and central nervous system dysfunction (MESH:D006331), liver failure (MESH:D017093), infected (MESH:D007239), CD (MESH:D003424), toxicity (MESH:D064420), renal tubular injury (MESH:D015499), atherosclerotic (MESH:D050197), viral diseases (MESH:D014777), death (MESH:D003643)
- **Chemicals:** teichoic acids (MESH:D013682), alpha-MEM (MESH:C420642), NO (MESH:D009569), ethanol (MESH:D000431), water (MESH:D014867), PGE2 (MESH:D015232), TRIzol (MESH:C411644), thiobarbituric acid (MESH:C029684), xylazine hydrochloride (MESH:D014991), pentobarbital (MESH:D010424), streptomycin (MESH:D013307), NaCl (MESH:D012965), T (MESH:D014316), paraffin (MESH:D010232), oxygen (MESH:D010100), phosphate (MESH:D010710), nitrate (MESH:D009566), tryptophan (MESH:D014364), RNS (MESH:D011886), lysophosphatidylcholine (MESH:D008244), HU (MESH:D006918), eosin (MESH:D004801), AMK (MESH:C032131), calcium (MESH:D002118), ROS (MESH:D017382), phosphoryl choline (MESH:D010767), Betadine (MESH:D011206), creatinine (MESH:D003404), formaldehyde (MESH:D005557), SYBR Green (MESH:C098022), GSH (MESH:D005978), CO2 (MESH:D002245), polypropylene (MESH:D011126), lipid (MESH:D008055), LPS (MESH:D008070), nitrite (MESH:D009573), urea (MESH:D014508), MDA (MESH:D008315), GSSG (MESH:D019803), H&amp;E (MESH:D006371), MEL (MESH:D008550), superoxide (MESH:D013481), CM-Dil (-), H2O2 (MESH:D006861), hematoxylin (MESH:D006416), penicillin (MESH:D010406)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Rattus norvegicus (brown rat, species) [taxon 10116], Homo sapiens (human, species) [taxon 9606]
- **Cell lines:** HUVEC-C — Homo sapiens (Human), Finite cell line (CVCL_2959)

## Figures

9 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12964371/full.md

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Source: https://tomesphere.com/paper/PMC12964371