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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Surgical and radiologic anatomy 15 (1993), S. 151-154 
    ISSN: 1279-8517
    Keywords: Double superior vena cava ; Azygos vein ; Human variation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Résumé Il a été observé un cas de double veine cave supérieure avec absence de la veine brachio-céphalique gauche. La veine cave supérieure gauche continuait la veine hémiazygos accessoire sans anastomose avec le sinus coronaire. Toutefois, le sang de la veine cave supérieure gauche se drainait dans la veine cave supérieure droite par une anastomose transverse entre les azygos droite et gauche. On pense que, 1) la veine inter-précardinale ne s'est pas formée, et 2) la veine précardinale gauche ne se continue pas dans la veine cardinale commune mais plutôt se draine dans l'azygos gauche. Ce cas doit reprśenter l'un des dispositifs les plus primitifs du système cave supérieur.
    Notes: Summary A case of double superior vena cava lacking the left brachiocephalic vein was found. The left superior vena cava directly continued to the accessory hemiazygos vein without anastomosis with the coronary sinus. Therefore, the blood from the left superior vena cava drained into the right superior vena cava via the transverse anastomosis between the left and right azygos lines. It was thought that embryologically 1) the inter-precardinal vein was not formed, and 2) the left precardinal vein did not continue to the common cardinal vein, rather it drained into the left azygos line. This case may represent one of the most basic arrangements of the superior caval system.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    The journal of membrane biology 123 (1991), S. 33-41 
    ISSN: 1432-1424
    Keywords: eccrine ; sweat gland ; cell volume ; cholinergic ; Ca ; potassium ; chloride ; channels ; quinidine
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Summary The goal of the present study was to elucidate the ionic mechanisms by which cholinergic stimulation induces cell shrinkage in eccrine clear cells. Dissociated Rhesus monkey eccrine sweat clear cells were prepared by collagenase digestion of freshly isolated secretory coils and immobilized on a glass slide in a perfusion chamber at 30°C. The cell was visualized by light microscopy with differential interference contract (DIC) and was recorded with a video system (15,000× total magnification). The cell volume was calculated from the maximal cross section of the cell. Methacholine (MCh)-induced cell shrinkage, which was as much as 30% of resting cell volume, was dose dependent and pharmacologically specific. MCh-induced cell shrinkage was persistent in some cells but tended to partially wane with time in others. MCh-induced cell shrinkage was dependent on the chemical potential gradient for KCl, i.e., increasing [K] in the bath ([K] o ) from 5 to 120mm caused MCh to induce cell swelling, whereas removing [Cl] o at 120mm K partially restored the MCh-induced cell shrinkage. The interpolated null [K] o (medium [K] where the cell volume did not change by MCh) of 71mm agreed with the predicted [K] o,null. MCh-induced cell shrinkage was inhibited completely by 1mm quinidine (K-channel blocker) and partially by 1mm diphenylamine-2-carboxylic acid (DPC, a Cl-channel blocker), but not by 0.1mm ouabain or 0.1mm bumetanide, suggesting that MCh-induced cell shrinkage may be due to activation of both K and Cl channels with the resultant net KCl efflux down the chemical potential gradient. That Ca/calmodulin may be involved in cholinergic regulation of Cl and K channels is suggested because 10 μm ionomycin also induced cell shrinkage, MCh failed to induce cell shrinkage in a Ca-free medium after the endogenous Ca store was depleted, and (6-aminohexyl)-5-chlorol-naphthalenesulfonamide (W-7, a putative inhibitor of calmodulin) also inhibited MCh-induced cell shrinkage in a reversible manner.
    Type of Medium: Electronic Resource
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