Effects Of A Selective Histamine H₄R Antagonist On Inflammation In A Model Of Carrageenan-Induced Pleurisy In The Rat

Abstract

The histamine H₄ receptor (H₄R), recently cloned and identified, is a G-protein coupled histamine receptor family expressed in immune cells which plays an important role in inflammation. Recent data evidentiated that H₄R antagonists can decrease airway inflammation and hyperreactivity in animal models of asthma. In the present study we evaluated the effect of the selective H₄R antagonist JNJ7777120 (JNJ) in carrageenan-induced pleurisy, an in vivo model of inflammation, well characterized for cellular and molecular mechanisms. Intra-pleural administration of λ-carrageenan (1% w/v in 0.2 ml sterile saline) determined an intense recruitment of leucocytes in pleural exudates and in lung tissues, activated inducible nitric oxide (NO) synthase and cyclooxygenase-2, thus increasing the generation of harmful autacoids such as NO and pro-inflammatory prostaglandins, PgE₂ and 6-ketoPgF(1α), increased cellular and DNA oxidative stress, measured as malondialdehyde and 8-OH-deoxyguanosine and the local generation of IL-1β and TNF-α. Moreover, the activity of caspase-3, an early marker of apoptosis was also activated by λ-carrageenan injection. The pre-treatment with JNJ (5-10 mg Kg⁻¹ b.wt., given intrapleurally), 60 min before carrageenan markedly reduced all the studied parameters. This study clearly demonstrated that histamine H₄R antagonists have anti-inflammatory effects and could have potential therapeutic application for the treatment of inflammatory diseases.

Modulation of Dendritic Cell Apoptosis and CD8+Cytotoxicity by Histamine: Role of Protein Kinase C

“…In our system, HIS was able to inhibit the levels of both the inactive and active forms of caspase-3 in DC. In a model of carrageenan-induced pleurisy in rats, the induction of an inflammatory response was associated with the recruitment of leukocytes and nitric oxide production, which together with the activation of caspase-3 upregulated oxidative damage and apoptosis [ 31 ]. The use of an H4R antagonist reversed dramatically the tissue injury.…”