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1.
Int Immunopharmacol ; 26(1): 272-6, 2015 May.
Article in English | MEDLINE | ID: mdl-25682766

ABSTRACT

We evaluated the clinical improvement of patients with mild to moderate persistent allergic rhinitis (AR) due to mono-sensitization to house dust mite (HDM) allergen, by sodium cromoglycate nasal spray (Lomusol 4%). Lomusol was used as a single agent treatment, and its anti-inflammatory effects, in the early phase reaction were evaluated. Herein we showed that Lomusol significantly improved the subjective nasal symptom scores especially nasal obstruction. This was associated with significant and specific reduction in neutrophils influx in nasal cytology but had no effect on other cell types. This selective anti-inflammatory effect on nasal cytology was associated with significant reduction in the levels of platelet activating factor (PAF) and histamine in nasal secretions but had no effect on PGD2, LTC4 or CysLt levels. Lomusol was also able to induce significant reduction in eosinophil cationic protein (ECP) levels in nasal secretions without altering the percentage of eosinophil influx in nasal cytology. Taken collectively, we showed the first evidence that nasal sodium cromoglycate possesses a selective inhibition on neutrophil recruitment into nasal cytology in the early phase reaction of AR patients mono-sensitized to HDM. This may be attributed to the ability of Lomusol to significantly reduce the amount of PAF recovered in nasal secretion. These results were associated with significant improvement in subjective symptom scores especially nasal obstruction that may in addition, be due to the ability of Lomusol to down-regulate eosinophil degranulation activity as well.


Subject(s)
Anti-Allergic Agents/therapeutic use , Cromolyn Sodium/therapeutic use , Pyroglyphidae/immunology , Rhinitis, Allergic/drug therapy , Administration, Intranasal , Adult , Animals , Anti-Allergic Agents/administration & dosage , Cromolyn Sodium/administration & dosage , Female , Humans , Male , Nasal Mucosa/drug effects , Nasal Mucosa/immunology , Nasal Provocation Tests , Neutrophil Infiltration/drug effects , Rhinitis, Allergic/diagnosis , Rhinitis, Allergic/immunology , Severity of Illness Index , Treatment Outcome
2.
J Biol Chem ; 288(2): 1374-84, 2013 Jan 11.
Article in English | MEDLINE | ID: mdl-23168411

ABSTRACT

We explored the relation between vasoactive intestinal peptide (VIP), CRTH2, and eosinophil recruitment. It is shown that CRTH2 expression by eosinophils from allergic rhinitis (AR) patients and eosinophil cell line (Eol-1 cells) was up-regulated by VIP treatment. This was functional and resulted in exaggerated migratory response of cells against PGD2. Nasal challenge of AR patients resulted in a significant increase of VIP contents in nasal secretion (ELISA), and the immunohistochemical studies of allergic nasal tissues showed significant expression of VIP in association with intense eosinophil recruitment. Biochemical assays showed that VIP-induced eosinophil chemotaxis from AR patients and Eol-1 cells was mediated through the CRTH2 receptor. Cell migration against VIP was sensitive to protein kinase C (PKC) and protein kinase A (PKA) inhibition but not to tyrosine kinase or p38 MAPK inhibition or calcium chelation. Western blot demonstrated a novel CRTH2-mediated cytosol-to-membrane translocation of PKC-ε, PKC-δ, and PKA-α, -γ, and -IIαreg in Eol-1 cells upon stimulation with VIP. Confocal images and FACS demonstrated a strong association and co-localization between VIP peptide and CRTH2 molecules. Further, VIP induced PGD2 secretion from eosinophils. Our results demonstrate the first evidence of association between VIP and CRTH2 in recruiting eosinophils.


Subject(s)
Eosinophilia/pathology , Eosinophils/cytology , Hypersensitivity/pathology , Receptors, Immunologic/metabolism , Receptors, Prostaglandin/metabolism , Trachea/pathology , Vasoactive Intestinal Peptide/metabolism , Amino Acid Sequence , Base Sequence , DNA Primers , Enzyme-Linked Immunosorbent Assay , Eosinophilia/metabolism , Flow Cytometry , Humans , Hypersensitivity/metabolism , Immunohistochemistry , Molecular Sequence Data , Reverse Transcriptase Polymerase Chain Reaction , Trachea/metabolism , Vasoactive Intestinal Peptide/chemistry
3.
Arch Facial Plast Surg ; 10(5): 346-9, 2008.
Article in English | MEDLINE | ID: mdl-18794414

ABSTRACT

OBJECTIVE: To investigate the anatomophysiologic aging-related changes in the orbicularis oculi muscle. METHODS: We examined the full-thickness histologic characteristics of the upper eyelids from cadavers of 30-, 40-, 60-, and 70-year-old men and the muscle interference pattern (IP) of 68 healthy volunteers of both sexes aged 18 to 73 years. RESULTS: Histologic analysis revealed that in the aging upper eyelid, changes were primarily in the skin and subcutaneous layers with the characteristic loss of collagen elastic fibers; however, the whole muscle layer was histologically intact, with no signs of aging; loss of fibers, loss of adherence to surrounding structure, or ptosis. Neurophysiologic studies of the electromyographic IP of the orbicularis oculi muscle confirmed that the full efficiency of orbicularis oculi function was intact in the age group studied (18-73 years) in both sexes. CONCLUSION: Our results suggest that the anatomophysiologic characteristics of the orbicularis oculi muscle remain intact through advancement of age.


Subject(s)
Aging/physiology , Eyelids/cytology , Adult , Aged , Female , Humans , Male , Middle Aged
4.
Int J Gen Med ; 1: 27-31, 2008 Nov 30.
Article in English | MEDLINE | ID: mdl-20428403

ABSTRACT

We recently reported a novel neuro-immuno co-operation between vasoactive intestinal peptide (VIP) and fraktalkine (FKN) in recruiting human mast cells to the asthmatic airway that provided a classical example of priming effect on mast cells migratory function, but the role of the F-actin in human mast cell chemotaxis' priming is poorly defined. Therefore the aim of this study was to further investigate the biophysical role of the cytoskeletal element; the F-actin, intracellular reorganization and its polymerization in mast cell priming of chemotaxis function. In the present communication it is shown by immunofluoresence confocal microscopy analysis that physical F-actin intracellular reorganization in a membrane bound manner on human mast cell is involved in VIP-induced priming of human mast cell chemotaxis against FKN. The F-actin reorganization was calcium independent and without modification of its contents as assessed by fluorescence-activated cell scanning analysis. These results identify a novel role for the biophysical association of F-actin in the crosstalk between neuro-inflammatory mediators and mast cells and may be an important target for therapeutic modalities in allergic inflammation.

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