Dopaminergic effect of anisodamine on the microcirculation of the hydronephrotic kidney of rats

Zou Ai-ping , Niranjan Parekh , Michael Steinhausen

Current Medical Science ›› 1991, Vol. 11 ›› Issue (2) : 65 -72.

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Current Medical Science ›› 1991, Vol. 11 ›› Issue (2) : 65 -72. DOI: 10.1007/BF02888091
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Dopaminergic effect of anisodamine on the microcirculation of the hydronephrotic kidney of rats

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Abstract

Anisodamine is an alkaloid extracted from the Tibetan plant “Anisodus tanguticus”. Since 1965 it has been used in China for the treatment of shock but the mechanisms of its action are not fully known. The present study was performed to determined the effect of anisodamine on the renal microcirculation and to examine the underlying mechanism of its actions. The addition of anisodamine (10−8 M to 10−3 M) to the kidney bath resulted in a significant and dose dependent dilation of all preglomerular vessels. The maximal dilation (about 30 % dilation) was found in the proximal interlobular artery. In contrast to preglomerular vessels anisodamine caused constriction of postglomerular vessels. The glomerular blood flow increased by about 50 % at anisodamine concentration of 10−3 M. Haloperidol, a dopamine receptor antagonist could abolish the renal vascular effect of anisodamine. It is suggested that anisodamine could improve renal function by the dilation of preglomerular vessels in combination with the constriction of postglomerular vessels, and the effect of anisodamine may be mediated by activation of the dopaminergic system.

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Zou Ai-ping, Niranjan Parekh, Michael Steinhausen. Dopaminergic effect of anisodamine on the microcirculation of the hydronephrotic kidney of rats. Current Medical Science, 1991, 11(2): 65-72 DOI:10.1007/BF02888091

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References

[1]

Department of Pediatrics, Peking Friendship Hospital. Anisodamine in treatment of some diseases with manifestations of acute microcirculatory insufficiency. Chinese Med J, 1975, 1: 127-32

[2]

(654–2) 1985,16:317–22.

[3]

SuJY, et al.. Beneficial effect of anisodamine in hemorrhagic shock. Naunyn-Schmiedeberg’s Arch Pharmacol, 1984, 325: 360-5

[4]

SuJY, et al.. Experimental study in rabbits of the antishock effect of anisodamine (654–2) and its mechanism of action. Resuscitation, 1983, 10: 173-84

[5]

654–2 1982; 44–8.

[6]

1982;11-27.

[7]

SteinhausenM, et al.. Hydronephrosiss: A new method to visualize vas afferens, efferens and glomerular network. Kidney Int, 1983, 23: 794-806

[8]

SteinhausenM, et al.. Response of in vivo renal microvesseis to dopamine. Kidney Int, 1986, 30: 361-70

[9]

BührleCh Ph, et al.. The afferent glomerular arterioie: Immunochemical and electrophysiological investigations. J Cardiovasc Pharmacol, 1984, 6: S383-93

[10]

BührleCh Ph, et al.. Intracellular recording in ju xt a glomerular granulated cells of the mouse kidney. Pflügers Archiv, 1984, 400: R21-R21

[11]

NobilingR, et al.. The hydronephrotic kidney of the mouse as a tool for intravital microscopy and in vitro electrophysiological studies of renincontaining cells. Pflügers Archiv, 1984, 400: R23-R23

[12]

IntagliettaM, et al.. Capillary flow velocity in vivo and in situ by television methods. Microvasc Res, 1975, 10: 165-79

[13]

SteinhausenM, et al.. Angiotensin I control of the renal microcirculation: Effect of blockade by saralasin. Kidney Int, 1986, 30: 56-61

[14]

ParekhN, VeithU. Renal hemodynamics and oxygen consumption during postischemic acute renal failure in the rat. Kidney Int, 1981, 19: 306-16

[15]

SteinhausenM. WheltonA. Intravital microscope observation of acute renal failure as a tool for simultaneously analyzing structure and function. Acute Renal Failure: correlation between morphology and function, 1984Kim SolezMarcel Dekker Inc.169-76

[16]

SteinhausenM, et al.. Pathophysiological mechanisms of acute renal failure. Contr Nephrol, 1981, 25: 151-6

[17]

OkenDE. Hemodynamic basis for human acute renal failure (vasomotor nephropathy). Am J Med, 1984, 76: 702-7

[18]

1980,19:303–5.

[19]

Department of Pharmacology, Chinese Academy of Medical Sciences. Pharmacologic effects of anisodamine. Chinese Med J, 1975, 1: 133-8

[20]

Marin-GrezM, et al.. Atrial natriuretic peptide causes preglomerular vasodilation and postglomerular constriction in rat kidney. Nature, 1986, 324: 473-6

[21]

Marin-GrezM, et al.. Dopamine receptor antagonists inhibit the natriuretic response to atrial natriuretic factor (ANF). Life Sci, 1985, 36: 2171-6

[22]

PettersonA, et al.. The diuretic effect of atrial natriuretic peptide (ANP) is dependent on dopaminergic activation. Acta Physiol Scand, 1986, 126: 619-21

[23]

1981;13:277–81.

[24]

1985; 17:161–4.

[25]

NicholsAJ, HileyCR. Identification of adrenoceptors and dopamine receptor mediating vascular responses in the superior mensenteric arterial bed of the rat. J Pharm Pharmacol, 1985, 37: 110-5

[26]

YehBK, et al.. Attenuation of dopamine renal and mesentric vasodilation by haloperidol: evidence for a specific dopamine receptor. J Pharmacol Exp Ther, 1969, 168: 303-9

[27]

FullerRW, et al.. Elevation of serum corticosterone in rats by dopamine agonists related in structure to pergolide. Neuroendocrinology, 1983, 36: 285-90

[28]

FullerRW, SnoddyHD. Serum corticosterone elevation by pergolide in rats: Prevention of tolerance development by spiperone. J Pharm Pharmacol, 1982, 34: 607-8

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