SUMMARY To study the effect of histamine (HA) on brain blood flow and capillary permeability, bilateral parietal craniectomies were made in cats anesthetized with nitrous oxide and ketamine. The dura was reraored and solutions of HA in mock cerebrospinal fluid (CSF) in varying concentrations ranging from 10 ' M to 10 ' M were irrigated continuously onto the exposed brain while local cerebral blood flow was determined polarographically by hydrogen clearance. Capillary permeability was assessed by determining HA's effect on the 12s I-albumin space of the brain. Electrical activity was monitored by eiectrocorticography. HA consistently dilated pial blood vessels and produced within 15 rain a dose-related local hyperemia that subsided 30-60 min after HA was removed. Hyperemia was blocked by cimetidine. HA had no appreciable effect on either the blood-brain barrier to albumin or the electrical activity of the cortex. HA is pharmacologically capable of participating directly in the acute hyperemic response of the brain's microclrculatlon to physiologic and pathologic stimuli but has little effect on cerebrovascular permeability to protein.Stroke, Vol 11, No 5, 1980MAMMALIAN BRAIN contains biologically significant amounts of histamine (HA) in 2 principal locations: within certain neurons, particularly those of the hypothalamus, and within mast cells, which tend to be concentrated in the leptomcninges.
'2 Neuronal HA probably functions as a neurotransmitter through a specific adenylate cyclase system that has pharmacologic properties of an H, receptor.3 The function of HA in the mast cells of the brain is unknown. Mast cells are often found in brain strategically located close to blood vessels where they may affect vascular tone and, in turn, cerebral blood flow.s Schwartz 4 has suggested that mast cell HA in the bnin plays a role in inflammatory processes and vascular control, as it does elsewhere in the body.The effect of HA on systemic vasculature has been well studied.1 ' 6 -' Injected intravenously, HA constricts cardiac and pulmonary arteries and dilates the capillary bed of peripheral organs where blood pools, leading to a fall in systemic arterial pressure. Concurrently, plasma is lost through the capillary endothelium, which accentuates shock.1 '' Injected subcutaneously, HA produces capillary hyperemia, increased vascular permeability and edema, thus mimicking, in part, the acute vascular response to injury. 1 ' ° Although considerable information is also available about the effect of HA on cerebrovascular smooth muscle and cerebral blood flow (CBF), much of it is contradictory. brain as it does the permeability of vessels outside of the central nervous system.Because of the continuing uncertainty regarding the preponderant effect of HA on CBF, the lack of information about the effect of HA on the permeability of cerebral blood vessels, and the evidence indicating biologically significant stores of HA in the brain, we undertook this in vivo study to determine the local response of the cerebral circulation of t...