Skip to content

Phencyclidine, Lysergic Acid Diethylamide, and Mescaline: Cerebral Artery Spasms and Hallucinogenic Activity

Bella T. Altura, Burton M. Altura

Science May 29, 1981 DOI: 10.1126/science.7195070 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Experimental study Peer reviewed
Population Isolated basilar and middle cerebral arteries
Interventions Phencyclidine Lysergic acid diethylamide Mescaline Verapamil
Topics LSD Mescaline
Keywords Phencyclidine Hallucinogen Psychotomimetic Pharmacology Antagonist Cerebral arteries Anesthesia
Citations 81
Key findings PCP, LSD, and mescaline produce cerebrovasospasm via distinct receptors, and verapamil reverses PCP-induced vasospasm.

Abstract

Phencyclidine (PCP), lysergic acid diethylamide (LSD), and mescaline produced potent contractile responses on isolated basilar and middle cerebral arteries, where, in terms of potency, LSD > mescaline > PCP. All three drugs produced cerebrovasospasm in a concentration range which parallels that needed for their psychotomimetic and intoxicating actions. Specific receptors for PCP, which subserve contraction and differ from those for LSD and mescaline, are found in cerebral arteries. Concentrations of PCP that produced near-maximum contractile responses on cerebral arteries were similar to those in the blood and brain of human subjects who had died from PCP overdoses. A specific calcium antagonist, verapamil, readily prevented (and reversed) PCP-induced vasospasm. This study provides direct evidence for PCP receptors in cerebral blood vessels, the biologic action of which can be reversed by a calcium antagonist; the clinical use of the latter could prove invaluable in treating PCP-intoxicated victims.

Explore topics