Search Results (754)

Retinitis pigmentosa (RP) is a genetically heterogeneous group of inherited retinal degenerative disorders characterized by progressive photoreceptor loss and vision impairment, for which broadly applicable mutation-independent therapies remain limited. To examine the therapeutic potential of combined galanin receptor 3 (GALR3) inhibition and antioxidant therapy in a mutation-independent context, we utilized the rd10 mouse model of RP. We first evaluated the effects of individual treatments with the GALR3 antagonist SNAP-37889 and the antioxidant quercetin, followed by a combined treatment regimen to determine whether simultaneous targeting of neuroinflammatory and oxidative stress pathways provides enhanced retinal protection. Treatment efficacy was assessed using functional and morphological analyses, including electroretinography (ERG) to measure retinal function, optical coherence tomography (OCT) to evaluate retinal structure in vivo, and histological and immunohistochemical analyses to quantify photoreceptor survival and markers of retinal oxidative stress and inflammation. Although the expression levels of individual inflammatory and oxidative stress markers did not consistently exhibit additive responses, the combined treatment produced greater photoreceptor survival and preservation of photopic retinal function than either monotherapy alone. These findings support the hypothesis that simultaneous modulation of oxidative stress and neuroinflammation provides greater neuroprotective benefits, establish a foundation for the development of mutation-independent therapeutic strategies for RP, and identify GALR3 as a promising therapeutic target. Full article

The withdrawal of antibiotic growth promoters has fundamentally changed the priorities of poultry nutrition, shifting attention from growth promotion towards maintenance of intestinal homeostasis and physiological resilience, defined here as the capacity of the organism to maintain or restore functional homeostasis when exposed to biological, nutritional, or environmental challenges. Although plant-derived feed additives have attracted considerable interest as natural alternatives, their biological activity is still commonly interpreted as a collection of independent antimicrobial, antioxidant, or immunomodulatory effects. This fragmented perspective may not fully capture the interconnected and context-dependent nature of their effects across experimental models. This review develops an integrated conceptual framework in which phytogenic feed additives are considered as potential systems-level modulators of the microbiota–gut–immune axis rather than as isolated sources of bioactive compounds. We synthesise experimental evidence from 155 broiler chickens identified through searches of PubMed, Web of Science, Scopus, and Google Scholar from database inception to June 2026, covering microbial ecology, intestinal morphology and barrier function, microbial metabolites, redox balance, inflammatory signalling, and innate and adaptive immunity across infectious, nutritional, and environmental challenge models. Particular attention is given to the different levels of evidence provided by culture-based and targeted analyses, microbiome profiling, integrated host–microbiome studies, and multi-omics approaches. The available evidence suggests that structurally diverse phytochemicals can influence overlapping regulatory networks linking microbial ecology, epithelial barrier integrity, redox balance, inflammatory signalling, and immune function. However, the magnitude and direction of these responses vary substantially according to botanical source, phytochemical composition, dose, formulation, duration of supplementation, animal genotype, basal diet, and experimental challenge. Collectively, the available evidence supports a paradigm shift from compound-centred interpretation towards network-based regulation of host homeostasis. Within this context, physiological resilience refers to the capacity to maintain or restore functional homeostasis in response to biological, nutritional, or environmental challenges. It may emerge from coordinated interactions among the intestinal microbiota, the epithelial barrier, and the immune system. Phytogenic supplementation may contribute to resilience by simultaneously modulating several components of this network, although causal relationships remain incompletely established for many proposed mechanisms. This systems-level perspective provides a framework for integrating heterogeneous evidence and for identifying priorities for future research, including dose–response relationships, phytochemical combinations, longitudinal multi-omics approaches, and validation under commercially relevant production conditions, with implications for precision poultry nutrition. Full article

Vitamin D and its metabolite 25-hydroxyvitamin D₃ (25-OH-D₃) are central to calcium homeostasis, maternal skeletal integrity, and sow reproductive efficiency. This study compared vitamin D₃ with an equivalent supranutritional dose of chemically or microbially produced 25-OH-D₃ from day 90 of gestation to weaning. A total of 100 Large White × Landrace sows were assigned to five treatments (n = 20): a basal control (25 µg/kg vitamin D₃), a VD₃ group (basal + 50 µg/kg vitamin D₃), and three 25-OH-D₃ groups (basal + 50 µg/kg 25-OH-D₃; QV1–QV3). Reproductive traits, colostrum composition, serum vitamin D-related indices, antioxidant and cytokine profiles, pre-weaning piglet growth, femoral mineral concentration, intestinal morphology, and barrier-related gene expression were assessed. Compared with the control, QV2 increased litter weight gain from birth to day 14 by 9.8%, piglet serum 25-OH-D₃ at weaning by 33.2%, and femoral calcium concentration by 14.4% (p < 0.05); litter and average piglet weights at weaning were unchanged. Maternal 25-OH-D₃ supplementation also altered the overall redox profile and several circulating inflammatory cytokines, increased jejunal and ileal villus height in the QV2 and QV3 groups, and upregulated selected tight-junction-related genes, including occludin and ZO-1, in a source- and intestinal-segment-dependent manner (p < 0.05). Responses were source-dependent, and QV2 showed the strongest effects for selected endpoints; the data do not support class-wide superiority of biosynthesized preparations. Full article

Background/Objectives: Immune-mediated inflammatory skin diseases (IMSDs), including psoriasis, atopic dermatitis, and systemic sclerosis, are chronic relapsing disorders that impose substantial physical, psychological, and economic burdens. Current assessment relies largely on subjective clinical scoring and conventional imaging modalities that provide limited functional information. This structured narrative review evaluates photoacoustic imaging (PAI) as a non-invasive optical-ultrasound technique for morphological and functional assessment in IMSDs. Methods: We searched PubMed studies published from January 2017 to December 2025 using terms related to photoacoustic imaging, optoacoustic mesoscopy, psoriasis, atopic dermatitis, systemic sclerosis, contact dermatitis, and immune-mediated inflammatory skin disease. Studies were narratively synthesized by disease, PAI modality, comparator, outcome, and translational limitation. Main Findings: PAI can map vascular and pigment-related optical absorption and estimate oxygenation, blood volume, and selected structural biomarkers. In psoriasis, atopic dermatitis, and systemic sclerosis, PAI-derived measures have been associated with clinical severity, subclinical vascular or epidermal changes, and treatment response. However, most available studies are small, single-center, heterogeneous, or based on prototype systems, and several biomarkers still require histopathological and external validation. Conclusions: Current evidence supports PAI as a feasible research and potential adjunctive assessment tool for IMSDs rather than an established replacement for standard clinical, histopathological, or imaging methods. Standardized protocols, validation across skin phototypes, cost-effective devices, and prospective multicenter studies are required before routine clinical adoption. Full article

Objective: Self-assembling peptide nanomaterials are increasingly investigated as modular platforms for vaccine delivery and immune modulation. However, their structure-dependent interactions with immune cells remain insufficiently defined, limiting their early evaluation as peptide nanomaterial. This study evaluated the physicochemical properties and immunological effects of three Sup35 G7-derived self-assembling peptide nanomaterials, G7, G7d, and G7d(PEG)HER2, with particular attention to innate immune compatibility and macrophage responses. Methods: The morphology and surface charge of the peptides were characterized by transmission electron microscopy and zeta-potential analysis. Their cytocompatibility was assessed in THP-1 macrophages, Jurkat T cells, and IM-9 B cells. Transcriptomic and proteomic analyses were integrated to identify immune-cell-specific molecular responses. Cellular uptake, apoptosis, cytokine secretion, and intracellular reactive oxygen species production were further examined in macrophages. In vivo immunization in BALB/c mice was conducted to assess systemic immunoglobulin responses. Results: G7 and G7d assembled into large crystalline aggregates with limited dispersibility, whereas PEGylated G7d(PEG)HER2 formed more uniform nanofibers. All three materials showed positive zeta potentials and relatively low cytotoxicity across the tested immune cell models. Among these cells, macrophages displayed the strongest molecular responses. Integrated transcriptomic and proteomic analyses revealed coordinated alterations mainly involving metabolic remodeling, redox homeostasis, proteasome activity, and mitochondrial-associated pathways, rather than predominant activation of classical pro-inflammatory signaling. Ultrastructural analysis confirmed intracellular uptake of assembled peptides and mitochondrial morphological changes without detectable apoptosis. Cytokine profiling showed reduced secretion of multiple cytokines and chemokines, while G7 induced higher intracellular reactive oxygen species than G7d and G7d(PEG)HER2. In vivo, G7d administration was associated with increased serum IgG levels, whereas G7 showed a moderate effect and G7d(PEG)HER2 exhibited minimal changes; IgM levels remained unchanged. Conclusions: Sup35 G7 based self-assembling peptides exhibit low acute toxicity but induce structure-dependent modulation of macrophage function. Differences in assembly morphology and surface modification may influence systemic humoral responses. These findings support the importance of physicochemical design in evaluating immune compatibility of peptide nanomaterial scaffolds. Full article

Although resistance exercise effectively attenuates disuse muscle atrophy, studies examining both quantitative muscle morphometry and transcriptomic responses during early adaptation remain limited. To comprehensively evaluate these adaptations, we performed automated Hematoxylin and Eosin stain (H&E)-based quantitative morphometry alongside transcriptomic profiling in a mouse model of hindlimb immobilization with or without resistance exercise. Resistance exercise partially restored muscle fiber atrophy and restored muscle morphology. Transcriptomic profiling identified 76 differentially expressed genes and revealed coordinated alterations involving metabolic regulation, immune/inflammatory responses, and extracellular matrix remodeling, rather than a single dominant signaling pathway. Functional enrichment analysis further highlighted cytokine-mediated signaling, extracellular matrix organization, and metabolic pathways associated with the early response to resistance exercise. Together, these findings demonstrate that automated H&E-based morphometry, alongside transcriptomic profiling, provides complementary structural and molecular insights into the early adaptive response to resistance exercise and offers a practical framework for future studies of skeletal muscle remodeling. Full article

Retinal degeneration is characterized by progressive photoreceptor loss driven by oxidative stress and chronic inflammation, yet effective mutation-independent therapeutic strategies remain limited. Lycium barbarum polysaccharides (LBPs) possess antioxidant and anti-inflammatory activities; however, the structural features responsible for their retinal protective effects remain poorly defined. In this study, crude LBP was fractionated by DEAE-cellulose ion-exchange chromatography, and the most bioactive fraction, LBPF2, was identified using H₂O₂-injured 661W cone photoreceptor-like cells. LBPF2 was subsequently characterized by high-performance anion-exchange chromatography, SEC-MALLS-RI, GC–MS methylation analysis, and one- and two-dimensional NMR spectroscopy, and its protective effects were evaluated in H₂O₂-treated 661W cells and rd10 mice. LBPF2 was identified as a homogeneous glucose-rich polysaccharide with an average molecular weight of approximately 41 kDa and a backbone mainly composed of →4)-α-D-Glcp-(1→ and →4,6)-α-D-Glcp-(1→ residues. LBPF2 reduced oxidative stress, inflammation, and apoptosis in H₂O₂-treated 661W cells, preserved retinal morphology, improved electroretinographic responses and partial retention of rhodopsin immunoreactivity relative to untreated rd10 mice, and restored redox homeostasis in rd10 mice. Pharmacological inhibition of Nrf2 using ML385 attenuated these protective effects, supporting the involvement of Nrf2/HO-1 signaling. Collectively, these findings identify LBPF2 as a structurally characterized neuroprotective polysaccharide that mitigates retinal degeneration through coordinated regulation of oxidative stress and inflammation and highlight its therapeutic potential for retinal degenerative diseases. Full article

Peri-implantitis is characterized by progressive tissue destruction accompanied by dysregulated innate and adaptive immune responses. This study evaluated whether systemic treatment with 2-deoxy-D-glucose (2-DG) could attenuate experimental peri-implantitis and alter inflammatory markers associated with macrophage- and T-cell-mediated responses in a rat model. Experimental peri-implantitis was induced in Sprague–Dawley rats by Porphyromonas gingivalis-inoculated silk ligation around the implant neck. After disease induction, animals received intraperitoneal injections of 2-DG or normal saline for six weeks while ligature-associated challenge was maintained. Peri-implant tissues were assessed by micro-computed tomography (micro-CT), hematoxylin and eosin staining, immunohistochemistry (IHC), and reverse transcription-quantitative PCR (RT-qPCR). 2-DG treatment significantly reduced peri-implant bone resorption and was associated with less pronounced bone-resorptive morphology. RT-qPCR showed lower expression of M1-associated genes (CD86, iNOS, TNF-α, IL-6, and IL-18) and the Th17-associated genes IL-17 and RORγT, whereas IL-21, M2-associated genes, and the Treg-associated gene FOXP3 were not significantly changed. IHC showed qualitative trends toward lower iNOS- and IL-17-positive signals. These findings provide proof-of-concept evidence that 2-DG treatment reduces peri-implant bone loss and is associated with attenuated inflammatory changes and lower expression of M1- and Th17-associated inflammatory markers in experimental peri-implantitis. This study supports further investigation of 2-DG as a potential immunometabolic adjunct for peri-implantitis management. Full article

Diffusion-weighted imaging (DWI) has evolved from a niche research sequence into an increasingly valuable adjunct to conventional magnetic resonance imaging (MRI) in musculoskeletal (MSK) radiology. By providing qualitative and quantitative information on tissue microstructure through assessment of water diffusion and apparent diffusion coefficient (ADC) mapping, DWI offers functional insights beyond conventional morphological imaging. We aim to present the current evidence for DWI in MSK imaging organised around established applications and emerging applications, with particular emphasis on composition-related interpretive pitfalls relevant to differentiating tumours and other pathologies, and to review the technique’s evolving role in routine practice. This narrative review synthesises the current literature on the clinical utility of DWI in MSK imaging. It is structured in four parts: foundations and the tissue composition signal framework, including the basis of qualitative and quantitative assessment; established applications; emerging applications; and assessment of tissue composition-related interpretive as well as technical pitfalls, including those arising due to myxoid matrix, chondroid matrix, blood degradation products, organising thrombus, crystalline or mineralised material, keratinaceous debris, purulent content, cellular haematopoietic marrow, by using original cases from the authors’ institution, which have been confirmed either histologically or surgically. Applications are stratified by strength of evidence. Established applications of DWI include soft tissue abscess detection, differentiation of malignant from benign soft tissue tumours, differentiation of malignant from benign vertebral compression fractures, and myeloma staging and response assessment, as well as treatment response in soft tissue and bone sarcomas. Whole-body MRI with DWI for staging and response assessment in multiple myeloma is guideline-endorsed and supported by prospective multicentre data. Soft tissue abscess detection, soft tissue and bone tumour characterisation, and characterisation of vertebral compression fractures are supported by consistent evidence from multiple independent cohorts, although no universally transferable ADC threshold exists. The emerging applications, which are promising adjuncts supported by small, single-centre or heterogeneous studies with thresholds that have not been externally validated, include ADC ghost sign in osteomyelitis (high specificity but sensitivity of only 20%), peripheral nerve sheath tumour characterisation and surveillance in NF1 patients, peripheral neuropathy and plexopathy, predisposing conditions such as Li Fraumeni syndrome in paediatric cancers, inflammatory myopathy, and postsurgical assessment of residual disease, as well as opportunistic detection of venous thrombosis. Radiomics and machine learning approaches remain experimental. Recent technical advances, including reduced field-of-view imaging, multi-shot acquisition and improved fat suppression, have mitigated but not eliminated historical limitations of susceptibility artefacts and limited spatial resolution. DWI has become an important functional imaging technique that complements conventional MRI across a broad range of musculoskeletal disorders. Understanding the relationship between tissue composition and the diffusion signal is central to both interpreting DWI correctly and avoiding its characteristic pitfalls. DWI is best regarded not as a stand-alone technique but as one component of a multiparametric assessment, in which its functional information is integrated with conventional morphological imaging. Ongoing technical improvement and expanding clinical evidence are expected to further support its integration into routine MSK imaging and its development as a quantitative biomarker for diagnosis, prognostication, and treatment monitoring. Full article

Objectives: This study aimed to explore the cellular injury phenotypes induced by outer membrane vesicles (OMVs) from uropathogenic Escherichia coli (E. coli, UPEC) and Proteus mirabilis (P. mirabilis, P. m) in human renal tubular epithelial HK-2 cells in vitro. Introduction: In urological practice, UPEC and P. mirabilis are representative pathogens of uncomplicated and complicated UTIs, respectively. Both are Gram-negative bacteria, and a notable feature of these bacteria is their ability to secrete OMVs. OMVs are nanoscale vesicles containing lipopolysaccharides (LPS), phospholipids, peptidoglycan, nucleic acids, and various virulence factors such as proteases and toxins. OMVs serve as effective carriers, delivering these toxic substances to host cells, triggering inflammatory responses, cellular damage, and ultimately cell death. Methods: In this study, we cultured standard pathogenic strains of E. coli and P. mirabilis in lysogeny broth (LB) medium until they reached the logarithmic growth phase. OMVs were isolated and identified. The uptake of OMVs by HK-2 cells was observed in vitro, and we evaluated the cytotoxic effects of both types of OMVs by measuring cell viability, oxidative stress, membrane permeability, mitochondrial function, and organelle morphology. Results: The results demonstrated that OMVs from both bacterial strains were efficiently internalized by HK-2 cells. Both OMVs induced oxidative stress, decreased antioxidant capacity, disrupted membrane permeability, and damaged mitochondrial function, leading to cell injury. Interestingly, while the two types of OMVs caused comparable cytotoxicity in terms of cell viability, oxidative stress and mitochondrial membrane potential, they produced distinct patterns of mitochondrial ultrastructural injury: P. mirabilis OMVs primarily caused mitochondrial structural deformation and blurred cristae, while E. coli OMVs led to mitochondrial swelling, cristae breakage, and vacuolization. These findings provide phenotypic evidence and experimental clues for understanding OMV-associated renal tubular epithelial injury caused by different uropathogens. Full article

Melatonin, a methoxyindole synthesized by the pineal gland, is secreted in response to photoperiodic cues relayed from the retina through an endogenous circadian oscillator within the suprachiasmatic nucleus. Consequently, melatonin secretion regulates the circadian rhythm. Melatonin has been reported to have antioxidant, photoprotective, anti-inflammatory, anticancer, and wound-healing properties. It has also been reported to promote hair growth, although the underlying mechanisms remain unclear. In this study, we explored the potential molecular mechanisms of melatonin-induced hair growth by using an in vivo C57BL/6 mouse model. We observed morphological changes in the dorsal area and changes in the hair cycle and anagen induction were observed through hematoxylin–eosin staining. The molecular mechanisms were explored using Western blotting and immunofluorescence assay. Our findings indicate that topical melatonin promotes anagen entry and hair regrowth in C57BL/6 mice, accompanied by the modulation of Wnt/β-catenin-related signaling proteins. The decrease in grayscale value, increase in hair length and skin thickness and histological change in hair follicles in the melatonin-treated group indicated hair regrowth in the dorsal skin of mice. Moreover, the expression of the Wnt/β-catenin pathway was remarkably regulated. These findings further our understanding of the molecular mechanisms underlying topical melatonin-induced hair growth. Full article

Aqueous Chlorella extract (CE) is a functional feed additive derived from widely cultivated microalgae. It is rich in proteins, polysaccharides, pigments, polyunsaturated fatty acids, vitamins and other bioactive compounds. CE possesses great potential to improve the health status and physiological performance of aquatic animals. This study investigated the effects of dietary CE on inflammatory response, non-specific immunity, antioxidant capacity, lipid metabolism, immune gene expression, intestinal histomorphology and intestinal microbiota in Litopenaeus vannamei. Shrimp were fed diets containing 0%, 1%, or 5% CE for 60 days. The 1% CE treatment produced stronger responses in several non-specific immune and antioxidant-related indicators and induced broader changes in immune-related gene expression. In contrast, the 5% CE treatment showed more pronounced changes in inflammation-related factors, lipid metabolism, and intestinal morphology. CE supplementation also altered intestinal microbial composition and predicted microbial functions, with different response patterns between the two inclusion levels. A distinctive feature of this study is the integrated identification of inclusion-level-specific response patterns across host physiological and intestinal microbial endpoints, rather than a simple increase in effects with increasing CE inclusion. Overall, the 1% treatment was more closely associated with immune and antioxidant-related responses, whereas the 5% treatment was more closely associated with anti-inflammatory, lipid-regulatory, and intestinal effects. These findings demonstrate the potential of CE as a functional aquafeed additive for improving aquatic animal health and provide a scientific basis for its application in sustainable shrimp aquaculture. Full article

Background: Diabetic foot ulcers (DFUs) are chronic wounds characterized by persistent inflammation, oxidative stress, impaired angiogenesis, and defective extracellular matrix remodeling. Current therapeutic approaches remain insufficient for refractory diabetic wounds due to limited drug retention and inadequate regulation of the wound microenvironment. This study aimed to develop a centipede-derived protein fraction-loaded nanocapsule hybrid hydrogel for sustained bioactive delivery and diabetic wound repair. Methods: A bioactive protein fraction was isolated from processed medicinal centipede material and screened using cellular compatibility assays. The selected tropomyosin-containing protein fraction was incorporated into nanocapsules and subsequently integrated into a gallic acid-modified polyacrylamide hydrogel matrix. The physicochemical properties, antioxidant activity, rheological behavior, and protein release characteristics of the nanocapsule-hydrogel system were systematically evaluated. A streptozotocin-induced diabetic rat wound model was established to assess therapeutic efficacy through wound closure analysis, histological staining, and immunohistochemical evaluation. Results: The prepared nanocapsules exhibited a spherical morphology, nanoscale size distribution, and sustained protein delivery capability. The PAM-GA hydrogel demonstrated antioxidant activity, injectability, shear-thinning behavior, self-healing ability, and enhanced retention of protein release. In vivo experiments showed that the PT@NC@PAM-GA hydrogel significantly accelerated wound closure and promoted tissue regeneration, accompanied by enhanced angiogenesis, collagen deposition, and reduced inflammatory responses. Conclusions: The centipede-derived protein fraction-loaded nanocapsule hybrid hydrogel effectively integrates bioactive protein delivery with a multifunctional hydrogel matrix, providing a potential strategy for sustained treatment of diabetic foot ulcers. Full article

Wle vanillin is widely used as a flavoring agent in food products, its potential as a non-antibiotic feed additive for broilers remains unexplored. This study primarily investigated the effects of dietary supplementation of vanillin on antioxidant activity, anti-inflammatory response, immune function, and gut microbiota composition in broilers. One-day-old male broilers were randomly assigned to five groups: a basal diet group, a positive control group (basal diet + 100 mg/kg chlortetracycline (CTC)), and three vanillin-supplemented groups (0.1%, 0.2%, or 0.4%) for 42 days. Results showed that vanillin improved antioxidant capacity, with elevated serum superoxide dismutase (SOD) and glutathione peroxidase (GSH-Px) activity and reduced malondialdehyde (MDA) levels. Broilers receiving vanillin supplementation showed lower levels of pro-inflammatory cytokines (interleukin-6 (IL-6), interleukin-1β (IL-1β), and tumor necrosis factor-α (TNF-α)) and higher interleukin-10 (IL-10) expression compared with controls. Additionally, serum immunoglobulin A (IgA) and immunoglobulin M (IgM) levels were also greater in the vanillin group. It also enhanced intestinal health by increasing the duodenal villus height-to-crypt depth ratio, improving intestinal morphology, raising the Firmicutes-to-Bacteroidetes ratio, and promoting Lactobacillus proliferation compared with CTC. Notably, growth performance data were exploratory in nature; vanillin was associated with numerical improvements in average daily gain (ADG) and feed conversion (F/G) ratio. These preliminary findings suggest that vanillin requires further investigation as a potential feed additive. Full article

Red tilapia (Oreochromis sp.) fry are routinely transported between hatcheries and grow out farms, yet the effects of transport duration on epidermal barrier-associated responses and goblet cells remain poorly defined. This study assessed the impact of simulated transport on epidermal morphology, immune-related gene expression and goblet cell density in red tilapia fry. Fish were assigned to four groups (0, 5, 12 and 20 h of transport). Skin samples were analyzed for relative mRNA expression of 10 genes associated with tight junction proteins, mucins, antimicrobial peptides and cytokines using RT-qPCR, and for epidermal goblet cell density by histology. Transport significantly modulated eight genes, forming three co-expression clusters associated with inflammatory, barrier-related, and mucus-related responses, with mainly non-linear time courses. MUC2, DB-4, IL-1β, and TGF-β1b showed transient increases at 5–12 h, whereas MUC5AC and claudin transcripts increased earlier and approached control levels at 20 h. Goblet cell density remained relatively stable up to 12 h but declined after 20 h, coinciding with changes in MUC2 and MUC5AC expression and suggesting altered mucosal responses during prolonged transport. Overall, transport durations ≤ 12 h were associated with relatively stable epidermal responses, whereas 20 h induced pronounced changes in goblet cell density and barrier-associated gene expression. These findings provide information that may assist future optimization of transport practices in tilapia aquaculture. Transport stress in red tilapia fry induces rapid defensive responses, significantly modulating gene expression and mucosal dynamics; this is characterized by increased mucus production, goblet cell density, and early upregulation of mucins (MUC2), followed by later increases in tight junction genes and anti-inflammatory cytokines, alongside a temporary downregulation of antimicrobial peptides. Full article