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. 2001 Dec 18;99(1):501–506. doi: 10.1073/pnas.012506099

Figure 2.

Figure 2

Release of endogenous norepinephrine (NE) from guinea pig heart synaptosomes by depolarization with 3–30 mM K+ in the absence and presence of the selective H3R agonist imetit (100 nM), either alone or in combination with the selective H3R antagonist thioperamide (300 nM). Points represent mean increases in norepinephrine release above the basal level (± SEM; n = 8). The basal norepinephrine level was 1.14 ± 0.01 pmol/mg of protein. *, P < 0.05 from the corresponding control norepinephrine level by unpaired t test.