Modulation of mesenteric collecting lymphatic contractions by σ₁-receptor activation and nitric oxide production

Abstract

Recently, it has been reported that a σ-receptor antagonist could reduce inflammation-induced edema. Lymphatic vessels play an essential role in removing excess interstitial fluid. We tested the hypothesis that activation of σ-receptors would reduce or weaken collecting lymphatic contractions. We used isolated, cannulated rat mesenteric collecting lymphatic vessels to study contractions in response to the σ-receptor agonist afobazole in the absence and presence of different σ-receptor antagonists. We used RT-PCR and Western blot analysis to investigate whether these vessels express the σ 1 -receptor and immunofluorescence confocal microscopy to examine localization of the σ 1 -receptor in the collecting lymphatic wall. Using N-nitro-l-arginine methyl ester (l-NAME) pretreatment before afobazole in isolated lymphatics, we tested the role of nitric oxide (NO) signaling. Finally, we used 4-amino-5-methylamino-2′,7′-difluorofluorescein diacetate fluorescence as an indicator to test whether afobazole increases NO release in cultured lymphatic endothelial cells. Our results show that afobazole (50–150 µM) elevated end-systolic diameter and generally reduced pump efficiency and that this response could be partially blocked by the σ 1 -receptor antagonists BD 1047 and BD 1063 but not by the σ 2 -receptor antagonist SM-21. σ 1 -Receptor mRNA and protein were detected in lysates from isolated rat mesenteric collecting lymphatics. Confocal images with anti-σ 1 -receptor antibody labeling suggested localization in the lymphatic endothelium. Blockade of NO synthases with l-NAME inhibited the effects of afobazole. Finally, afobazole elicited increases in NO production from cultured lymphatic endothelial cells. Our findings suggest that the σ 1 -receptor limits collecting lymphatic pumping through a NO-dependent mechanism. NEW & NOTEWORTHY Relatively little is known about the mechanisms that govern contractions of lymphatic vessels. σ 1 -Receptor activation has been shown to reduce the fractional pump flow of isolated rat mesenteric collecting lymphatics. The σ 1 -receptor was localized mainly in the endothelium, and blockade of nitric oxide synthase inhibited the effects of afobazole.