Key result
Propranolol antagonized the hypotensive effect of alpha-blockers, increasing MAP to 20% above control, but did not reverse hypotension induced by sodium nitroprusside or methacholine.
Why the study?
Does propranolol antagonize hypotension induced by alpha-blockers, sodium nitroprusside, or methacholine in conscious unrestrained rats?
Does propranolol antagonize hypotension induced by alpha-blockers, sodium nitroprusside, or methacholine in conscious unrestrained rats?
Propranolol specifically antagonizes the hypotensive effect of alpha-blockers but not sodium nitroprusside or methacholine, suggesting a specific interaction between alpha- and beta-antagonists.
Animal data suggest specific alpha-beta antagonist interaction in rats; hypothesis-generating and should not change practice.
A pressor response has been observed with propranolol, a nonselective beta-adrenoceptor antagonist, in animals given a nonselective alpha-adrenoceptor antagonist. This study investigates whether a pressor response to propranolol occurs in conscious unrestrained rats following a hypotensive response induced by phentolamine (nonselective alpha-antagonist), prazosin (selective alpha 1-antagonist) and (or) rauwolscine (selective alpha 2-antagonist), sodium nitroprusside (smooth muscle relaxant), or methacholine (muscarinic agonist). The rats were subjected to a continuous infusion of a hypotensive agent or normal saline followed by i.v. injection of propranolol. The infusion of phentolamine significantly decreased mean arterial pressure (MAP). Subsequent injection of propranolol restored MAP to the control level. Prazosin and rauwolscine each caused a small but not significant decrease in MAP which was reversed by propranolol. Concurrent infusions of prazosin and rauwolscine caused a significant decrease in MAP. Subsequent injection of propranolol caused a large pressor response which increased MAP to 20% above control MAP prior to the administration of drugs. Nitroprusside or methacholine each caused a significant decrease in MAP, but the hypotension was not antagonized by propranolol. The concurrent infusions of a low dose of nitroprusside and prazosin caused a significant decrease in MAP which was reversed by propranolol. The infusion of saline did not alter MAP, and propranolol did not cause a pressor response. It is concluded that propranolol antagonizes the hypotensive effect of an alpha-blocker but not that of sodium nitroprusside or methacholine. Our results suggest the presence of a specific interaction between alpha- and beta-antagonists.
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Tabrizchi et al. (1989) studied this question. Propranolol vs. Normal saline was evaluated on Mean arterial pressure (MAP). Propranolol antagonized the hypotensive effect of alpha-blockers, increasing MAP to 20% above control, but did not reverse hypotension induced by sodium nitroprusside or methacholine.
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