Sodium binding in the arterial wall

1969 ◽  
Vol 47 (9) ◽  
pp. 763-770 ◽  
Author(s):  
Vladimír Palatý ◽  
Brigid Gustafson ◽  
Sydney M. Friedman

There are two fractions of sodium in the arterial wall which can be selectively and reversibly exchanged for other ions. These fractions are believed to be bound to the acid mucopolysaccharide – protein component of the paracellular matrix. The first fraction seems to be loosely bound by weakly acidic groups, probably the carboxyl groups of the hexuronic acid moieties. It can be exchanged for hydrogen even in neutral solutions by reducing the concentration of sodium ions in the medium. In the rat tail artery, the average size of this fraction did not exceed 0.5 meq/100 g of dry fat-free tissue. The second fraction behaves as if it is more tightly bound, apparently by strongly acidic groups like the sulfo groups of the mucopolysaccharides. It amounts to 2.21 ± 0.20 meq/100 g of dry fat-free tissue if a simplified system of sodium and calcium chloride solutions is used. In the presence of normal plasma concentrations of potassium and magnesium, the sum of both sodium fractions is increased substantially and is equal to approximately 5 meq/100 g of dry fat-free tissue. This bound sodium is increased in arteries of immature animals and animals with established DOCA hypertension, both of which have a higher content of the acid mucopolysaccharides.

1973 ◽  
Vol 51 (6) ◽  
pp. 410-417 ◽  
Author(s):  
S. M. Friedman ◽  
M. Nakashima ◽  
V. Palatý ◽  
B. K. Walters

The changes in the resistance of the perfused ventral rat-tail artery resulting from exposure of the tissue to ouabain-containing and/or K+-free physiological salt solution were studied. In each case, there was an increase in the vascular resistance which was not sustained. The response of the arterial wall to the above stimuli was abolished in the absence of external Ca2+. In contrast to the delayed response of the wall to either ouabain-containing or K+-free solution, an almost instantaneous rise in the resistance was observed if the two stimuli were combined, though the rate of loss of the tissue K+ was not accelerated significantly under these experimental conditions. The tension developed in K+-free solution was relieved almost instantaneously upon readmittance of external potassium.


2020 ◽  
Vol 182 ◽  
pp. 114263
Author(s):  
F. Fusi ◽  
P. Mugnai ◽  
A. Trezza ◽  
O. Spiga ◽  
G. Sgaragli

2007 ◽  
Vol 135 (1-2) ◽  
pp. 130
Author(s):  
James A. Brock ◽  
Diana Tripovic ◽  
Svetlana Pianova ◽  
Elspeth M. McLachlan

1991 ◽  
Vol 22 (2) ◽  
pp. 399-402 ◽  
Author(s):  
Xie-Nan Huang ◽  
Issei Takayanagi ◽  
Ryuichi Kurata ◽  
Tetsuhiro Hisayama

1980 ◽  
Vol 164 (3) ◽  
pp. 252-256 ◽  
Author(s):  
R. C. Webb ◽  
P. M. Vanhoutte ◽  
D. F. Bohr

2019 ◽  
Vol 316 (1) ◽  
pp. H89-H105 ◽  
Author(s):  
Somayeh Mojard Kalkhoran ◽  
Sarah Heather Jane Chow ◽  
Jagdeep Singh Walia ◽  
Cynthia Gershome ◽  
Nickolas Saraev ◽  
...  

ATP and norepinephrine (NE) are coreleased from peripheral sympathetic nerve terminals. Whether they are stored in the same vesicles has been debated for decades. Preferential dependence of NE or ATP release on Ca2+ influx through specific voltage-gated Ca2+ channel (Cav2) isoforms suggests that NE and ATP are stored in separate vesicle pools, but simultaneous imaging of NE and ATP containing vesicles within single varicosities has not been reported. We conducted an immunohistochemical study of vesicular monoamine transporter 2 (VMAT2/SLC18A2) and vesicular nucleotide translocase (VNUT/SLC17A9) as markers of vesicles containing NE and ATP in sympathetic nerves of the rat tail artery. A large fraction of varicosities exhibited neighboring, rather than overlapping, VNUT and VMAT2 fluorescent puncta. VMAT2, but not VNUT, colocalized with synaptotagmin 1. Cav2.1, Cav2.2, and Cav2.3 are expressed in nerves in the tunica adventitia. VMAT2 preferentially localized adjacent to Cav2.2 and Cav2.3 rather than Cav2.1. VNUT preferentially localized adjacent to Cav2.3 > Cav2.2 >> Cav2.1. With the use of wire myography, inhibition of field-stimulated vasoconstriction with the Cav2.3 blocker SNX-482 (0.25 µM) mimicked the effects of the P2X inhibitor suramin (100 µM) rather than the α-adrenergic inhibitor phentolamine (10 µM). Variable sensitivity to SNX-482 and suramin between animals closely correlated with Cav2.3 staining. We concluded that a majority of ATP and NE stores localize to separate vesicle pools that use different synaptotagmin isoforms and that localize near different Cav2 isoforms to mediate vesicle release. Cav2.3 appears to play a previously unrecognized role in mediating ATP release in the rat tail artery. NEW & NOTEWORTHY Immunofluorescence imaging of vesicular nucleotide translocase and vesicular monoamine transporter 2 in rat tail arteries revealed that ATP and norepinephrine, classical cotransmitters, localize to well-segregated vesicle pools. Furthermore, vesicular nucleotide translocase and vesicular monoamine transporter 2 exhibit preferential localization with specific Cav2 isoforms. These novel observations address long-standing debates regarding the mechanism(s) of sympathetic neurotransmitter corelease.


2002 ◽  
Vol 90 (7) ◽  
pp. 792-799 ◽  
Author(s):  
Karl Swärd ◽  
Karl Dreja ◽  
Anders Lindqvist ◽  
Erik Persson ◽  
Per Hellstrand

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