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利多卡因增强钡和铯诱导的肾上腺儿茶酚胺释放

Enhancement of barium- and cesium-induced adrenal catecholamine release by lidocaine.

作者信息

Borowitz J L, Shanbaky I

出版信息

Experientia. 1977 Apr 15;33(4):495-6. doi: 10.1007/BF01922231.

DOI:10.1007/BF01922231
PMID:871317
Abstract

Catecholamine release evoked from isolated perfused bovine adrenals by Ba+2 or Cs+ is enhanced by lidocaine or by a calcium-free medium. The action of Cs+ therefore differs from that of K+ or Rb+ in adrenal medulla. Divalent and monovalent metallic cations of relatively large atomic weight like Ba+2 and Cs+, probably penetrate the cell more easily than small highly charged ions and act intracellularly to cause adrenal catecholamine release. Local anesthetics and calcium-free media may allow greater influx of Ba+2 and Cs+ into adrenomedullary cells.

摘要

钡离子(Ba+2)或铯离子(Cs+)从离体灌注的牛肾上腺诱发的儿茶酚胺释放,会因利多卡因或无钙培养基而增强。因此,铯离子在肾上腺髓质中的作用不同于钾离子(K+)或铷离子(Rb+)。像钡离子和铯离子这样相对原子量大的二价和一价金属阳离子,可能比小的高电荷离子更容易穿透细胞,并在细胞内起作用导致肾上腺儿茶酚胺释放。局部麻醉剂和无钙培养基可能会使更多的钡离子和铯离子流入肾上腺髓质细胞。

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Experientia. 1977 Apr 15;33(4):495-6. doi: 10.1007/BF01922231.
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本文引用的文献

1
THE EFFECTS OF ALKALINE EARTHS AND OTHER DIVALENT CATIONS ON ADRENAL MEDULLARY SECRETION.碱土金属及其他二价阳离子对肾上腺髓质分泌的影响。
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2
STIMULANT ACTION OF BARIUM ON THE ADRENAL MEDULLA.钡对肾上腺髓质的刺激作用。
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3
Inhibition of catecholamine secretion and calcium exchange in perfused cat adrenal glands by tetracaine and magnesium.丁卡因和镁对灌注猫肾上腺中儿茶酚胺分泌及钙交换的抑制作用。
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Effects of alkali metal and other monovalent ions on the adrenomedullary secretion.碱金属及其他一价离子对肾上腺髓质分泌的影响。
Eur J Pharmacol. 1968 Jun;3(3):235-41. doi: 10.1016/0014-2999(68)90136-2.
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Duration of catecholamine release from bovine adrenal medulla.
Am J Physiol. 1971 May;220(5):1194-8. doi: 10.1152/ajplegacy.1971.220.5.1194.
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Biological membranes: the physical basis of ion and nonelectrolyte selectivity.生物膜:离子与非电解质选择性的物理基础。
Annu Rev Physiol. 1969;31:581-646. doi: 10.1146/annurev.ph.31.030169.003053.
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The membrane actions of anesthetics and tranquilizers.麻醉剂和镇静剂的膜作用。
Pharmacol Rev. 1972 Dec;24(4):583-655.
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Adrenal catecholamine release by divalent mercury and cadmium.
Arch Int Pharmacodyn Ther. 1974 May;209(1):94-9.