# Embryonic nano lauric acid delivery modulates lipid metabolism, oxidative balance, and gut morphogenesis in broiler chicks

**Authors:** Mostafa Mohamed Soliman, Saad N. El-Shater, Aya M. Yassin, Khaled Abo-EL-Sooud, Moataz Ibrahim, Gamal A. Swielim

PMC · DOI: 10.1038/s41598-026-38610-8 · 2026-03-03

## TL;DR

Injecting nano-lauric acid into chicken embryos improves their health and metabolism after hatching.

## Contribution

This study introduces nano-lauric acid as an effective in ovo treatment to enhance lipid metabolism and antioxidant defenses in broiler chicks.

## Key findings

- In ovo injection of 2.5 mg/egg nano-lauric acid improved lipid metabolism and increased HDL cholesterol in chicks.
- Nano-lauric acid upregulated antioxidant genes NRF2 and mt-SOD2, reducing oxidative stress in the liver.
- Intestinal development was enhanced with increased villus height and crypt depth in treated chicks.

## Abstract

The in ovo-injection technique was employed as an early-life nutritional strategy to improve the health and productivity of birds by delivering nutrients and bioactive compounds directly to the developing embryo. This study explored the innovative use of in ovo administration of nano-lauric acid (NLA) as a strategy for the metabolic programming of broiler chicks. The goal was to improve hatchability, stimulate hepatic antioxidant activity, regulate growth-related genes, and support intestinal development in newly hatched chicks. A total of 400 fertile eggs from a 40-week-old Arbor Acres breeder flock were randomly divided into four treatment groups: a non-injected control group (CN), a vehicle-injected control group (CP; 0.1 mL of sterile distilled water), and two NLA-treated groups receiving either 2.5 mg/egg (NLA 2.5) or 5 mg/egg (NLA 5) of NLA, each dissolved in 0.1 mL of sterile distilled water. Injections were administered into the yolk sac on day 12 of incubation. Post-hatching, the hatchability percentage was recorded. Serum lipid profiles, hepatic redox status, and the expression level of hepatic genes, nuclear factor erythroid 2–related factor 2 (NRF2), mitochondrial superoxide dismutase 2 (mt-SOD2), and insulin-like growth factors 1 and 2 (IGF-1 and IGF-2) were evaluated. Additionally, the intestinal morphology of the newly hatched chicks was examined. Hatchability % was significantly reduced in the NLA 5 group (80%) compared to the CN (98%), CP (97%), and NLA 2.5 (96%) groups. The findings showed that in ovo injection of NLA at 2.5 mg/egg was therefore identified as optimal, significantly improving lipid metabolism by reducing serum triglycerides, LDL, VLDL, and cholesterol, while increasing HDL cholesterol compared to controls (P < 0.05). Hepatic antioxidant defense was significantly improved through the decrease of malondialdehyde (MDA) and increase of reduced glutathione (GSH) concentrations (P < 0.05). This enhancement was associated with the upregulation of NRF-2 and mt-SOD2 by (4.04; 3.69-folds, respectively) and stimulation of anabolic signaling genes IGF-1 and IGF-2 by (4.08 and 2.3-folds; respectively) (P < 0.05). In addition, intestinal development has been significantly promoted via increased villus height and crypt depth (P < 0.05). Our findings demonstrate that in ovo NLA supplementation at 2.5 mg/egg effectively enhances lipid utilization, activates NRF2-mediated antioxidant pathways, and stimulates anabolic signaling. This targeted nutritional strategy proves to be a safe and effective method for pre-hatch metabolic programming, with significant potential to improve post-hatch health and performance in broilers.

## Linked entities

- **Genes:** GABPA (GA binding protein transcription factor subunit alpha) [NCBI Gene 2551], IGF1 (insulin like growth factor 1) [NCBI Gene 3479], IGF2 (insulin like growth factor 2) [NCBI Gene 3481]
- **Chemicals:** lauric acid (PubChem CID 3893), malondialdehyde (PubChem CID 10964), glutathione (PubChem CID 124886)
- **Species:** Gallus gallus (taxon 9031)

## Full-text entities

- **Genes:** LPL (lipoprotein lipase) [NCBI Gene 396219], IGF1 (insulin like growth factor 1) [NCBI Gene 418090] {aka IGF-1, IGF-I}, GHRL (ghrelin/obestatin prepropeptide) [NCBI Gene 408185] {aka ghrelin, preproghrelin}, MTOR (mechanistic target of rapamycin) [NCBI Gene 419455] {aka FRAP1}, ACTB (actin, beta) [NCBI Gene 396526] {aka Bact, actin}, IGF2R (insulin like growth factor 2 receptor) [NCBI Gene 395817] {aka MPR300}, TLR4 (toll like receptor 4) [NCBI Gene 417241], INSR (insulin receptor) [NCBI Gene 420133] {aka CTK-1}, GH (growth hormone) [NCBI Gene 378781] {aka GH1, cGH}, NFE2L2 (nuclear factor, erythroid 2 like 2) [NCBI Gene 396014] {aka ECH, NRF2}, NFE2L2 (NFE2 like bZIP transcription factor 2) [NCBI Gene 4780] {aka IMDDHH, NRF2, Nrf-2}, IGF2 (insulin like growth factor 2) [NCBI Gene 395097] {aka IGF-II}, IGF2 (insulin like growth factor 2) [NCBI Gene 3481] {aka C11orf43, GRDF, IGF-II, PP9974, SRS3}, SOD1 (superoxide dismutase 1, soluble) [NCBI Gene 395938], SOD2 (superoxide dismutase 2, mitochondrial) [NCBI Gene 374042] {aka MNSOD}, CAT (catalase) [NCBI Gene 423600], INS (insulin) [NCBI Gene 396145], IGF1R (insulin like growth factor 1 receptor) [NCBI Gene 395889] {aka IGF-1R}, IGF1 (insulin like growth factor 1) [NCBI Gene 3479] {aka IGF, IGF-I, IGFI, MGF}, OLFM4 (olfactomedin 4) [NCBI Gene 418826] {aka olfactomedin-4}
- **Diseases:** liver injury (MESH:D017093), gut (MESH:C536735), CP (MESH:D002972), dehydration (MESH:D003681), insulin resistance (MESH:D007333), weight gain (MESH:D015430), metabolic dysfunction (MESH:D008659), Marek's disease (MESH:D008380), cervical dislocation (MESH:D002575), inflammation (MESH:D007249)
- **Chemicals:** MCT (MESH:C000709826), sodium butyrate (MESH:D020148), GML (MESH:C020777), GSH (MESH:D005978), lipid (MESH:D008055), LPS (MESH:D008070), eosin (MESH:D004801), alcohol (MESH:D000438), formalin (MESH:D005557), ROS (MESH:D017382), CP (-), superoxide (MESH:D013481), H&amp;E (MESH:D006371), HMG-CoA (MESH:C008047), atorvastatin (MESH:D000069059), polyunsaturated fatty acid (MESH:D005231), hematoxylin (MESH:D006416), coconut oil (MESH:D000074263), amino acids (MESH:D000596), phosphotungstic acid (MESH:D010772), MDA (MESH:D008315), fatty acid (MESH:D005227), water (MESH:D014867), free fatty acids (MESH:D005230), LA (MESH:C030358), copper (MESH:D003300), 5,5'-dithiobis (2-nitrobenzoic acid) (MESH:D004228), Malic acid (MESH:C030298), cholesterol (MESH:D002784), ethanol (MESH:D000431), mevalonate (MESH:D008798), paraffin (MESH:D010232), fat (MESH:D005223), NaCl (MESH:D012965), linoleic acid (MESH:D019787), phosphate (MESH:D010710), Thiopentone (MESH:D013874), xylene (MESH:D014992), nitrogen (MESH:D009584), TG (MESH:D014280), carbon (MESH:D002244)
- **Species:** Gallus gallus (bantam, species) [taxon 9031], Acanthopagrus schlegelii (black porgy, species) [taxon 72011], gut metagenome (species) [taxon 749906], Coturnix coturnix (Common quail, species) [taxon 9091], Cyprinus carpio (carp, species) [taxon 7962], Sparus aurata (gilthead bream, species) [taxon 8175], Rattus norvegicus (brown rat, species) [taxon 10116], Rodentia (rodent, order) [taxon 9989], Homo sapiens (human, species) [taxon 9606]

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12960906/full.md

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Source: https://tomesphere.com/paper/PMC12960906