Takagi M, Kimura K, Atarashi K, Ikeda T, Matsuoka H, Ishii M, Sugimoto T
Second Department of Internal Medicine, Faculty of Medicine, University of Tokyo, Japan.
Am J Hypertens. 1990 Nov;3(11):838-45. doi: 10.1093/ajh/3.11.838.
In order to evaluate whether immunoglobulin deposition in vessels plays some role in the development of vascular lesions in severe hypertension, an immunohistochemical study was performed in spontaneously hypertensive rats (SHRs), to which deoxycorticosterone acetate (DOCA) and salt were administered. DOCA and salt rapidly induced severe hypertensive vascular lesions, including necrotizing arteriolitis and productive endarteritis. In these rats, considerable deposits of IgG and IgM were found in the small arteries and arterioles of the kidneys. These deposits were accompanied by complement (C3), and could be eluted by acid incubation. They were localized in periodic acid-Schiff-positive insudative lesions, which were thought to be an early phase of the hypertensive vascular lesions. These results suggest that the immunoglobulins might be bound to an unknown antigen in the vascular lesions and that some immunological mechanism mediated by the immunoglobulins is involved in the development of vascular lesions in severe hypertension.
为了评估血管内免疫球蛋白沉积是否在重度高血压血管病变的发展中起某种作用,对给予醋酸脱氧皮质酮(DOCA)和盐的自发性高血压大鼠(SHR)进行了免疫组织化学研究。DOCA和盐迅速诱发了重度高血压血管病变,包括坏死性小动脉炎和增殖性动脉内膜炎。在这些大鼠的肾脏小动脉和微动脉中发现了大量IgG和IgM沉积。这些沉积物伴有补体(C3),且可通过酸孵育洗脱。它们定位于高碘酸希夫染色阳性的渗出性病变中,这些病变被认为是高血压血管病变的早期阶段。这些结果表明,免疫球蛋白可能与血管病变中一种未知抗原结合,并且由免疫球蛋白介导的某些免疫机制参与了重度高血压血管病变的发展。