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Am J Physiol Heart Circ Physiol 292: H1821-H1827, 2007. First published December 8, 2006; doi:10.1152/ajpheart.00365.2006
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Lowering of interstitial fluid pressure after neurogenic inflammation in mouse skin is partly dependent on mast cells

Tine V. Karlsen, Athanasia Bletsa, Eli-Anne B. Gjerde, and Rolf K. Reed

Department of Biomedicine, University of Bergen, Bergen, Norway

Submitted 6 April 2006 ; accepted in final form 27 November 2006

Neurogenic inflammation is known to induce lowering of interstitial fluid pressure (Pif) in mouse skin. This study examined the possible role of mast cell activation secondary to neuropeptide release in lowering of Pif by using KitW/KitW-v mice, which are devoid of mast cells, including connective tissue mast cells (CTMCs). Pif was measured in paw skin of anesthetized (fentanyl-fluanison and midazolam, 1:1) mice with glass capillaries connected to a servo-controlled counterpressure system. In contrast to wild-type mice, intravenous administration of mast cell-activating compound 48/80 induced no lowering of Pif in KitW/KitW-v mice. Intravenous challenge with substance P (SP), calcitonin gene-related peptide (CGRP), or capsaicin induced a significant (P < 0.05) lowering of Pif in wild-type mice to –2.16 ± 0.28, –1.96 ± 0.11, and –2.22 ± 0.19 mmHg, respectively, compared with vehicle (–0.49 ± 0.11 mmHg). In KitW/KitW-v mice the Pif response to SP was completely abolished (–0.53 ± 0.32 mmHg) while the response to CGRP and capsaicin was attenuated (–1.33 ± 0.13 and –1.42 ± 0.13 mmHg, respectively) although significantly (P < 0.05) lowered compared with vehicle. Immunohistochemical analysis revealed no difference in distribution or density of SP- and CGRP-immunoreactive fibers in paws of KitW/KitW-v compared with wild-type mice. We conclude that lowering of Pif normally depends on mast cells. However, the sensory nerves can also elicit a lowering of Pif that is independent of mast cells.

KitW/KitW-v mice; neuropeptides; micropuncture



Address for reprint requests and other correspondence: T. V. Karlsen, Dept. of Biomedicine, Univ. of Bergen, Jonas Lies vei 91, N-5009 Bergen, Norway (e-mail:tine.karlsen{at}biomed.uib.no)




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