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Novel Non-Injection Approaches for Revealing and for Microscopic Investigation of the Microcirculatory Bed in Different Organs and Tissues

Published online by Cambridge University Press:  02 July 2020

N. Chilingaryan
Affiliation:
Department of Neurology, # 5637, LAC-USC Medical Center, 1200 N. State St., Los AngelesCA90033.
A. Chilingaryan
Affiliation:
Laboratory of Histochemistry and Neuromorphology, Institute of Physiology, Armenian Academy of Sciences, Yerevan, Armenia375028.
M. Chilingaryan
Affiliation:
Laboratory of Histochemistry and Neuromorphology, Institute of Physiology, Armenian Academy of Sciences, Yerevan, Armenia375028.
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Extract

Certain disadvantages of traditional injection methods and difficulties arising during investigation of experimental and pathological material, limit the possibilities for extensive study of the microcirculatory bed (MCB). This has prompted the authors to develop new non-injection methods for revealing the MCB on histological sections by means of direct staining of the structural elements of the vessel wall. These methods are based on selective precipitation of the extra- or intracellular orthophosphates with ions of Zn, Cd, Co, Ca, Sr, and Pb in the vascular endothelium and smooth muscle cells. These methods (which we have called “histoangiological”) provide clear-cut contrast dyeing of the MCB in different organs and tissues as well as tumors in rat, cat,pig, dog, and in humans.

In these methods, the reaction end product is lead sulfide which provides a high degree of contrast. Vessels and capillaries are detected due to precipitation of the deposit in the vascular endothelium.

Type
From Scanning Probe Microscopy to High Resolution Ultrasound: New Versions of the Vasculature
Copyright
Copyright © Microscopy Society of America 1997

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References

1.Veklich, Y.I.et al., J. Biol. Chem., 268(1993)13577.Google Scholar
2.Gorkun, O.V.et al., Biochemistry, 33(1994)6986.10.1021/bi00188a031CrossRefGoogle Scholar
3.Weisel, J.W.et al., J. Mol. Biol., 232(1993)285.10.1006/jmbi.1993.1382CrossRefGoogle Scholar
4.Collet, J.–P.et al., Biophys. J., 70(1996)500.10.1016/S0006-3495(96)79596-6CrossRefGoogle Scholar
5.Woodhead, J.L.et al., J. Biol Chem., 271(1996)4946.Google Scholar
6.Baradet, T.C.et al., Biophys. J., 68(1995)1551.10.1016/S0006-3495(95)80327-9CrossRefGoogle Scholar
7. I thank all of my colleagues and collaborators, especially Drs. Veklich, Nagaswami and Woodhead, and acknowledge the support of NIH grants HL30954 and RR2483 and of the University Research Foundation.Google Scholar