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. Author manuscript; available in PMC: 2023 Dec 5.
Published in final edited form as: Br J Pharmacol. 2021 Apr 30;178(13):2709–2726. doi: 10.1111/bph.15463

FIGURE 3.

FIGURE 3

Dose-dependent NO release for (a–d) compounds 5, 10, 11 and 25 in Be2C cells transfected with 7TM-μ receptors (7TM-MOR), 6TM-μ receptors (6TM-MOR), β2-adrenoceptors (β2-AR) or 6TM-MOR+β2-AR. (a) Compound 5 (n = 4, 4, 3 and 4 per dose tested in 7TM-MOR, 6TM-MOR, β2-AR and 6TM-MOR/β2-AR transfected cell line, respectively) induced a dose-dependent release of NO in 7TM-MOR transfected cells only. Compounds (b) 10 (n = 3, 4, 3 and 4 per dose tested in 7TM-MOR, 6TM-MOR, β2-AR and 6TM-MOR/β2-AR transfected cell line, respectively), (c) 11 (n = 3, 4, 3 and 4 per dose tested in 7TM-MOR, 6TM-MOR, β2-AR and 6TM-MOR/β2-AR transfected cell line, respectively) and (d) 25 (n = 3 for log doses −8.0, −7.0 and −6.0 per transfected cell line and n = 3, 5, 3 and 5 in 7TM-MOR, 6TM-MOR, β2-AR and 6TM-MOR/β2-AR transfected cell lines, respectively, for log doses −5.0, −4.3 and −4.0) induced a dose-dependent release of NO in 6TM-MOR transfected cells, and this effect was potentiated by co-transfection with β2-AR. None of the compounds released NO when the cells were transfected only with β2-AR. Data expressed as mean ± SEM