ABSTRACT
Prokineticin 2 (PK2) is a putative output molecule from the SCN. PK2 RNA levels are rhythmic in the mouse SCN, with high levels during the day, and PK2 administration suppresses nocturnal locomotor activity in rats. The authors examined the PK2 system in a diurnal rodent, Arvicanthis niloticus, to determine whether PK2 or PK2 receptors differ between diurnal and nocturnal species. The major transcript variant of A. niloticus PK2 (AnPK2) encodes a 26-residue signal peptide followed by the presumed mature peptide of 81 residues. Within the grass rat signal sequence, polymorphic sequences and amino acid substitutions were observed relative to mouse and laboratory rats, but the hydrophobic core and cleavage site of the signal sequence were preserved. The mature PK2 peptide is identical among A. niloticus, rat, and mouse. AnPK2 mRNA is rhythmically expressed in the SCN, with peak RNA levels occurring in the morning, preceding peaks of Per1 and Per2 as in mouse SCN. Analysis of prokineticin receptor 2 (PKR2) sequences revealed polymorphisms among the grass rats studied. PKR2 mRNA was expressed in the SCN and paraventricular nuclei of the thalamus and hypothalamus. While further analysis is necessary, there is no clear evidence indicating that a difference in the PK2 ligand/receptor system accounts for diurnality in this rodent species. These data contribute to a growing body of evidence suggesting that the key to diurnality lies downstream of the SCN in A. niloticus.
Subject(s)
Circadian Rhythm/genetics , Circadian Rhythm/physiology , Gene Expression Regulation/physiology , Amino Acid Sequence , Animals , Brain Chemistry/genetics , DNA, Complementary/biosynthesis , DNA, Complementary/genetics , In Situ Hybridization , Light , Male , Molecular Sequence Data , Polymorphism, Genetic/genetics , Rats , Rodentia , Transcription, Genetic , Vascular Endothelial Growth Factor, Endocrine-Gland-Derived/biosynthesis , Vascular Endothelial Growth Factor, Endocrine-Gland-Derived/geneticsABSTRACT
A 43-year-old white woman with a history of multiple ocular surgeries, including 4 penetrating keratoplasties, developed a concentric retrocorneal membrane at the graft periphery in the right eye. A white-light, tandem, scanning confocal microscope using a 24x/0.60 contact objective was used to examine the right eye in vivo. At the endothelial layer, confocal microscopic images similar to corneal epithelial cells were detected at the graft periphery. Unlike normal endothelial cells, the imaged cells demonstrated easily recognizable nuclei.
Subject(s)
Corneal Diseases/pathology , Epithelium, Corneal/pathology , Keratoplasty, Penetrating/adverse effects , Adult , Corneal Diseases/etiology , Female , Humans , Microscopy, ConfocalABSTRACT
Fourteen nonstrabismic volunteers were monocularly patched for 2 and 24 hours in separate experiments. Horizontal and vertical phorias were measured at 6 m and 30 cm, at 30-second intervals, for at least 30 minutes, following removal of the patch. After 24 hours of monocular occlusion, the initial change from baseline at 6 m ranged from 9.5 prism diopters exo to 7 delta eso and 6.5 delta hyper to 3 delta hypo. At 30 cm, the initial change ranged from 7.5 delta exo to 4 delta eso and 1 delta hyper to 1 delta hypo. In all but three subjects, phorias returned to within 2 delta of baseline by 3 minutes, and in all subjects by 25 minutes. After 2 hours of monocular occlusion, the range of initial change from baseline was similar to 24 hours of occlusion, but all phorias returned to within 2 delta of baseline by 2.5 minutes. Therefore, we suggest that ocular alignment should not be routinely measured within 3 minutes of removing a patch. If patched for 24 hours, a few individuals will require up to 25 minutes for stabilization of their deviation. Further studies might address these effects in patients with subnormal fusion and stereopsis.