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Pituitary adenylate cyclase-activating peptide receptor 1 mediates anti-inflammatory effects in allergic airway inflammation in mice.
Lauenstein, H D; Quarcoo, D; Plappert, L; Schleh, C; Nassimi, M; Pilzner, C; Rochlitzer, S; Brabet, P; Welte, T; Hoymann, H G; Krug, N; Müller, M; Lerner, E A; Braun, A; Groneberg, D A.
Afiliação
  • Lauenstein HD; Department of Immunology, Allergology and Immunotoxicology, Fraunhofer Institute for Toxicology and Experimental Medicine, Hannover, Germany.
Clin Exp Allergy ; 41(4): 592-601, 2011 Apr.
Article em En | MEDLINE | ID: mdl-21059121
ABSTRACT

BACKGROUND:

Bronchial asthma is characterized by airway inflammation and reversible obstruction. Since the gold standard of therapy, a combination of anti-inflammatory corticosteroids and bronchodilatory ß(2) agonists, has recently been discussed to be related to an increased mortality, there is a need for novel therapeutic pathways.

OBJECTIVE:

A new experimental concept that encompasses the vasoactive intestinal peptide/pituitary adenylate cyclase activating peptide (PACAP) family of receptors by demonstrating the anti-inflammatory effects of the PACAP receptor 1 (PAC1R) in a murine model of allergic asthma is described.

METHODS:

PAC1R expression was investigated in lung tissue and isolated dendritic cells (DCs) via real-time PCR. Ovalbumin (OVA)-induced asthma models were used in PAC1R-deficient mice and BALB/c mice treated with PAC1R agonist maxadilan (MAX). Bronchoalveolar lavages have been performed and investigated at the cellular and cytokine levels. Fluorescence staining of a frozen lung section has been performed to detect eosinophil granulocytes in lung tissue. Plasma IgE levels have been quantified via the ELISA technique. Lung function was determined using head-out body plethysmography or whole-body plethysmography.

RESULTS:

Increased PAC1R mRNA expression in lung tissue was present under inflammatory conditions. PAC1R expression was detected on DCs. In OVA-induced asthma models, which were applied to PAC1R-deficient mice (PAC1R(-/-)) and to BALB/c mice treated with the specific PAC1R agonist MAX, PAC1R deficiency resulted in inflammatory effects, while agonistic stimulation resulted in anti-inflammatory effects. No effects on lung function were detected both in the gene-depletion and in the pharmacologic studies. In summary, here, we demonstrate that anti-inflammatory effects can be achieved via PAC1R.

CONCLUSION:

PAC1R agonists may represent a promising target for an anti-inflammatory therapy in airway diseases such as bronchial asthma.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Pneumonia / Asma / Receptores de Polipeptídeo Hipofisário Ativador de Adenilato Ciclase / Hipersensibilidade Limite: Animals Idioma: En Ano de publicação: 2011 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Pneumonia / Asma / Receptores de Polipeptídeo Hipofisário Ativador de Adenilato Ciclase / Hipersensibilidade Limite: Animals Idioma: En Ano de publicação: 2011 Tipo de documento: Article