Research Note: Effect of light intensity of calcium homeostasis in pullets.

The impact of varying light intensities on layer pullets is not yet well understood. Behaviorally, brighter illumination may increase pullet activity levels by allowing better navigation in the complexity of non-cage systems. In addition, light intensity was previously demonstrated to affect the levels of calcium and phosphate regulating hormones in mice. The objective of this study was to examine how exposure of pullets to different light intensity affects their calcium and phosphorus homeostasis. Lohmann LSL-Lite and Lohmann Brown-Lite pullets were randomized into 4 individually controlled rooms with 6 pens per room, which were assigned to 10 or 50 lux light intensity supplied via white LED lighting during the photophase. After 8 and 16 wk of exposure, plasma calcium, phosphorus, and magnesium were measured by inductively coupled plasma optical emission spectrometry; and parathyroid hormone, 1,25-dihydroxyvitamin D, fibroblast growth factor 23, and markers of bone formation and resorption were measured by ELISA. Intestine and kidney samples were collected at 16 wk and gene expression of receptors for calcium and phosphate regulating hormones was assessed. The data were analyzed by one-way ANOVA. Lohmann Brown-Lite pullets exposed to 50 lux for 8 wk exhibited lower ionized Ca levels and a trend for increased bone formation markers compared to pullets reared in 10 lux. Thus, higher light intensity during rearing may beneficially affect calcium homeostasis and bone formation in young Lohmann Brown-Lite chicken.

Comparison of the effects of serpin A1, a recombinant serpin A1-IGF chimera and serpin A1 C-terminal peptide on wound healing.

Serpin A1 (alpha1-antitrypsin, alpha1-proteinase inhibitor), a potent neutrophil elastase inhibitor, has therapeutic potential as a wound-healing agent. We compared the in vitro wound-healing action of serpin A1-IGF, a recombinant fusion protein of serpin A1(M351E-M358L) and insulin-like growth factor I with that observed in the presence of natural serpin A1 or A1-C26, the synthetic C-terminal 26 residue peptide of serpin A1, previously shown to have mitogenic and antiviral activities. All agents reduced wound sizes in monolayers of the kidney epithelial cell line LLC-PK1 and in primary cultures of human skin fibroblasts. Wound reduction in primary human keratinocytes was only observed with the serpin A1-IGF chimera. None of the factors stimulated cell proliferation using a colorimetric assay, with the exception of the serpin A1-IGF chimera, which caused a significant increase of cell proliferation and thymidine incorporation in human skin fibroblasts. However, wound healing by the A1-IGF chimera was reduced in keratinocytes in the presence of mitomycin C, suggesting a role of cell proliferation in wound reduction. The hydrophobic A1-C26 peptide significantly increased the production of collagen I in skin fibroblasts, an appealing asset for skin care applications.