Nag S
Department of Pathology, Queen's University, Kingston, Ontario, Canada.
Acta Neuropathol. 1988;75(6):547-53. doi: 10.1007/BF00686198.
The plasma membrane calcium-activated adenosine triphosphatase (Ca2+-ATPase) is known to regulate intracellular calcium levels. This enzyme was localised in intracerebral cortical vessels of normotensive and acutely hypertensive rats. Of interest was whether the arterioles that develop increased permeability to horseradish peroxidase (HRP) in acute hypertension demonstrate any alteration in localisation of Ca2+-ATPase as compared to normotensive controls. Rats were injected with HRP intravenously and acute hypertension was induced by a 2-min infusion of angiotensin amide. Following perfusion of fixative, brains were sliced and reacted for demonstration of HRP reaction product and Ca2+-ATPase. Normotensive rats showed discontinuous distribution of Ca2+-ATPase on the outer plasma membranes of endothelial, smooth muscle and adventitial cells of arterioles. The localisation of Ca2+-ATPase in pinocytotic vesicles present in endothelial and smooth muscle cells was quite striking. Focal cortical areas of hypertensive rats showed increased arteriolar permeability to HRP. Permeable arterioles showed marked reduction of Ca2+-ATPase on the outer plasma membranes of endothelium and smooth muscle cells as compared to nonpermeable arterioles of the same animals and arterioles of normotensive controls. The latter finding suggests that calcium may be involved in increased cerebrovascular permeability mechanisms in acute hypertension.
已知质膜钙激活腺苷三磷酸酶(Ca2 + -ATP酶)可调节细胞内钙水平。该酶定位于正常血压和急性高血压大鼠的脑皮质血管中。有趣的是,与正常血压对照组相比,急性高血压时对辣根过氧化物酶(HRP)通透性增加的小动脉在Ca2 + -ATP酶定位上是否有任何改变。给大鼠静脉注射HRP,并通过2分钟输注血管紧张素酰胺诱导急性高血压。灌注固定剂后,将脑切片并进行反应以显示HRP反应产物和Ca2 + -ATP酶。正常血压大鼠的小动脉内皮细胞、平滑肌细胞和外膜细胞的外质膜上Ca2 + -ATP酶呈间断分布。Ca2 + -ATP酶在内皮细胞和平滑肌细胞中存在的胞饮小泡中的定位非常明显。高血压大鼠的局灶性皮质区域显示小动脉对HRP的通透性增加。与同一动物的非通透性小动脉和正常血压对照组的小动脉相比,通透性小动脉在内皮细胞和平滑肌细胞的外质膜上Ca2 + -ATP酶明显减少。后一发现表明,钙可能参与急性高血压时脑血管通透性增加的机制。