Key result
Canine mesencephalic stimulation reveals anatomically distinct vasoconstriction points for the kidney, intestine, and lower extremity.
Why the study?
Selective vasoconstriction of different vascular beds induced by mesencephalic stimulation and its anatomical specificity were unclear.
The mesencephalic pressor area contains anatomically distinct points that mediate selective vasoconstriction in different vascular beds.
Does not alter clinical practice; leaves open whether mesencephalic topography enables selective vasomotor control in humans.
In an attempt to clarify the selective vasoconstriction of different vascularbeds, vasoconstrictor responses of kidney, intestine and lower extremity to the electrical stimulation of the points within the mesencephalon were systematically explored. Three vascular circuits were perfused at constant flow, and changes in vascular resistance were indicated by changes in perfusion pressure. Various points were stimulated by moving electrode position, and systemic arterial pressure and perfusion pressure from 2 of these vascular circuits were simultaneously measured. Central stimulation caused systemic pressor and vasoconstrictor responses of varied degree in 3 vascular circuits. Slight shift in electrode position altered the vasoconstrictor response patterns in these vascular circuits. The points giving maximum systemic pressor and maximum vasoconstrictor responses in kidney, intestine and lower extremity were anatomically separate, though these points were located very closely each other. No anatomical separation was found in control group, both sides of renal or femoral circuits.
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UEDA et al. (1966) studied Normal physiology (animal model) (n=24). Electrical stimulation of the mesencephalic pressor area vs. Different stimulation sites within the mesencephalon was evaluated on Changes in perfusion pressures (vascular resistance) in the kidney, intestine, and lower extremity. Electrical stimulation of the mesencephalic pressor area in dogs revealed that the points giving maximal vasoconstriction in the kidney, intestine, and lower extremity were anatomically separate.
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