Key result
Combined glycopyrrolate and dexmedetomidine increased blood pressure (99 vs 90 mm Hg; P<0.05) but effectively inhibited norepinephrine release and MSNA, serving as an alternative to ganglionic blockade.
RCT
Randomized days
Answers are grounded in this paper and cite their sources.
May support sympathetic inhibition research as ganglionic blockade alternative; hypothesis-generating and should not yet change practice.
The purpose of this study was to compare ganglionic blockade with trimethaphan (TMP) and an alternative drug strategy using combined muscarinic antagonist (glycopyrrolate, GLY) and alpha-2 agonist (dexmedetomidine, DEX). Protocol 1: incremental phenylephrine was administered during control and combined GLY-DEX, or control and TMP on two control combined GLY and DEX or TMP infusion on two randomized days. Protocol 2: muscle sympathetic nerve activity (MSNA) and the baroreflex MSNA relationship was determined before and after GLY-DEX. Blood pressure was higher with GLY-DEX (99+/-3 mm Hg) and lower with TMP (78+/-3 mm Hg) relative to control (GLY-DEX: 90+/-2 mm Hg; TMP: 91+/-2 mm Hg; P<0.05). Incremental phenylephrine increased pressure during GLY-DEX (P<0.01 vs control) and TMP (P<0.01 vs control) to a similar degree. Both GLY-DEX and TMP infusion inhibited norepinephrine release (P<0.01 vs control). GLY-DEX inhibited baseline MSNA (P<0.05) and baroreflex changes in MSNA (P<0.01). We conclude that the GLY-DEX alternative drug strategy can be used as a reasonable alternative to pharmacologic ganglionic blockade to examine autonomic cardiovascular control.
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Wilkins et al. (2007) reported an RCT. Glycopyrrolate (GLY) and dexmedetomidine (DEX) vs. Trimethaphan (TMP) and control was evaluated on Blood pressure (p=<0.05). Combined glycopyrrolate and dexmedetomidine increased blood pressure (99 vs 90 mm Hg; P<0.05) but effectively inhibited norepinephrine release and MSNA, serving as an alternative to ganglionic blockade.
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