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NEUROHUMORAL CONTROL OF CARDIOVASCULAR FUNCTION
1Department of Physiology, Nagasaki University School of Medicine, Nagasaki 852-8523; 2Department of Anatomy and Physiology, Faculty of Wellness, Kwassui Women's College, Nagasaki 850-0954; and 3Natural Environmental Conservation, Faculty of Environmental Studies, Nagasaki University, Nagasaki 852-8521, Japan
Submitted 30 December 2003 ; accepted in final form 19 June 2004
The effect of intracerebroventricular infusion of compound 48/80 (C48/80), a mast cell secretagogue, on adrenal cortisol secretion was investigated in dogs under pentobarbital sodium anesthesia. A marked increase in adrenal cortisol secretion was elicited by C48/80 along with a concomitant increase in the plasma levels of cortisol and immunoreactive ACTH, but neither arterial blood pressure and heart rate nor the plasma histamine level altered significantly. Pretreatment with either anti-CRF antiserum or pyrilamine maleate (H1 histamine-receptor antagonist) significantly attenuated the C48/80-evoked increase in cortisol secretion, but pretreatment with metiamide (H2-receptor antagonist) significantly potentiated it. Significant attenuation of the C48/80-evoked increase in cortisol also occurred in dogs given ketotifen, a mast cell stabilizing drug, before pharmacologic challenge. In the pars tuberalis and median eminence (ME), mast cells were highly concentrated in close association with the primary plexus of the hypophysial portal system. Degranulated mast cells were extensively found in the ME of C48/80-treated animals. These results suggest that mast cells located in these regions liberated histamine within the brain as a result of degranulation induced by C48/80 and that this led to activation of the hypothalamic-pituitary-adrenocortical axis.
brain mast cells; cortisol; pyrilamine; metiamide; ketotifen
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I. Matsumoto, Y. Inoue, T. Shimada, T. Matsunaga, and T. Aikawa Stimulation of brain mast cells by compound 48/80, a histamine liberator, evokes renin and vasopressin release in dogs Am J Physiol Regulatory Integrative Comp Physiol, March 1, 2008; 294(3): R689 - R698. [Abstract] [Full Text] [PDF] |
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