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81.
目的: 研究心肌肽素对豚鼠心室肌细胞钠通道的影响,探讨心肌肽素在离子通道水平的作用机制。 方法: 用急性酶解分离法获得豚鼠心室肌细胞,标准全细胞膜片钳技术记录钠电流(INa)。 结果: 心肌肽素1、5、10、50、100、500 mg/L使豚鼠心室肌细胞INa分别减少(0±1)%、(6±2)%、(10±2)%、(15±1)%、(22±9)%、(30±6)%,呈浓度依赖性抑制INa。心肌肽素50 mg/L使INa激活时间(TTP)从(2.8±0.7) ms延长至(3.0±0.8) ms (P<0.05);使INa电流密度-电压曲线上移,但不改变激活电位、峰电位、反转电位和I-V曲线的形状;不影响稳态激活曲线、稳态失活曲线和稳态失活后恢复曲线。 结论: 心肌肽素浓度依赖性抑制豚鼠心室肌细胞INa,可能是其抗心律失常作用的机制之一。 相似文献
82.
The regulation of blood vessel diameter is under the control of the autonomic nervous system (as well as hormones and metabolites), sympathetic nerve stimulation evoking depolarizing post-synaptic potentials. Excitatory junction potentials (EJPs) were recorded from vascular smooth muscle cells of guinea-pig small mesenteric arteries (pressurized) following nerve stimulation. Repetitive stimulation (>5Hz) led to summation of EJPs, which evoked spikes and vasoconstriction. Replacing extracellular Na+ with choline (plus atropine) resulted in a decrease in EJP amplitude, but spike amplitude and maximum rate of rise (+Vmax) were unaffected. Decreasing the extracellular Ca2+ concentration produced decreases in EJP amplitude and spike +Vmax, while increasing extracellular Ca2+ resulted in increased EJP amplitude and spike +Vmax. Verapamil and bepridil, agents that depress Ca2+ influx in vascular and visceral smooth muscle, depolarized the membrane and depressed EJPs and spikes at high concentrations (10–5 M and 5×10–6 M, respectively). The data indicate that EJPs are dependent on external Na+ and Ca2+ ions, and that spikes are dependent on Ca2+. Thus, neuromuscular transmission in this muscle is similar to that in non-vascular smooth muscles, such as intestinal muscle and vas deferens.Part of this work has been presented to the Biophysical Society (Zelcer and Sperelakis 1980) and to the American Physiological Society (Zelcer and Sperelakis 1981) 相似文献
83.
Chana Yagil Gurion Katni Yoram Yagil 《Pflügers Archiv : European journal of physiology》1994,427(3-4):225-232
It has been previously demonstrated that adenosine induces natriuresis when administered directly into the renal circulation
of the rat. It was postulated that the mechanism was inhibition of tubule Na+ reabsorption. In the current study, the hypothesis was tested that adenosine inhibits ion reabsorption across the inner medullary
collecting duct (IMCD), a tubule segment which is rich in adenosine receptors. IMCD epithelium from rat kidney was grown in
primary culture as a confluent monolayer on Costar filters, allowing selective access to the basolateral and apical surfaces
of the cells. Transepithelial resistance was taken as a measure of epithelial permeability and ion conductance. Na+ uptake was studied using 22Na+ and used to determine the permeability of the epithelial monolayer specifically to Na+. Exposure of the basolateral aspect of the monolayer to adenosine (10−8–10−7 M) increased transepithelial resistance in a dose- and time-dependent manner; in parallel, adenosine (10−7–10−6 M) reduced apical Na+ uptake from 20±5 to 10±2 nmol/cm2. 1,3-Dipropyl-8-(2-amino-4-chlorophenyl)-xanthine (PACPX, 5×10−9 M), an adenosine antagonist with selectivity for the A1 receptor, inhibited the rise in transepithelial resistance and the decrease in Na+ uptake following the addition of adenosine. The effects of adenosine on transepithelial resistance were reproduced with the
A1 receptor selective adenosine analogue N
6-cyclohexyladenosine (CHA, 10−8 –10−7 M) but not with the A2 selective analogues, 5′-N-ethylcarboxamidoadenosine (NECA) or CGS 21680. CHA (10−7 M) inhibited apical Na+ uptake by 50%, an effect abolished by PACPX. The effects of adenosine on transepithelial resistance and Na+ uptake were inhibited, but only in part, by amiloride. These data suggest that adenosine inhibits ion movement, specifically
apical Na+ uptake, across the IMCD epithelium and that this effect is mediated by A1 receptors from the basolateral aspect of the cell. The results are consistent with the hypothesis that adenosine inhibits
Na+ reabsorption across the IMCD. 相似文献
84.
Micropuncture studies on the filtration rate of single superficial and juxtamedullary glomeruli in the rat kidney 总被引:28,自引:0,他引:28
Summary Single nephron filtration rates of superficial and juxtamedullary nephrons were determined in high and low sodium rats. Single nephron GFR was calculated from TF/P inulin and tubular flow rate in superficial nephrons and single juxtamedullary GFR from corresponding data in long loops of Henle. In low sodium rats superficial nephron GFR was 23.5±6.4 (SD)×10–6 ml/min×g KW, juxtamedullary nephron GFR was 58.2±13.6 and total kidney GFR (C
In) was 0.94±0.16 ml/min×g KW. Using these single nephron values, total kidney GFR and a total number of 30,000 glomeruli per kidney, the number of superficial and juxtamedullary glomeruli was calculated to be 23,267 and 6,733, respectively. During high sodium diet superficial nephron GFR increased to 38.1±11.3 and single juxtamedullary GFR decreased to 16.5±6.6, total kidney GFR increasing to 1.01±0.24. Calculation again revealed the same distribution of the two nephron types. End-proximal TF/P inulin in superficial nephrons was 2.36±0.36 in low sodium and 2.31±0.28 in high sodium rats. Loops of Henle TF/P inulin and intratubular flow rate were inversely related: the highest TF/P inulin values and lowest intratubular flow rates were found in the descending limb. These data quantify the distribution of superficial and juxtamedullary nephrons on a functional basis and suggest a mechanism by which the kidney adjusts sodium excretion by altering the contribution of each nephron type to total kidney GFR.Supported by the Deutsche Forschungsgemeinschaft and the U.S. Department of the Army, through its European Research Office. 相似文献
85.
Marguerite Hatch Robert W. Freel N. D. Vaziri 《Pflügers Archiv : European journal of physiology》1993,423(3-4):206-212
In order to characterize oxalate handling by the P2 segment of the rabbit proximal colon, the fluxes of [14C]oxalate, 22Na+, and 36Cl– were measured in vitro using conventional short-circuiting techniques. In standard buffer the proximal colon exhibited net secretion of Na+ (–2.31±0.64 equiv cm–2 h–1), negligible net Cl– transport, and net secretion of oxalate (–12.7±1.6 pmol cm–2 h–1). Replacement of buffer Na+ or Cl– abolished net oxalate secretion, while HCO
3
–
-free media revealed a net absorption of oxalate (19.3±4.2 pmol cm–2 h–1) and stimulated NaCl absorption. Mucosal amiloride and dimethylamiloride (1 mM) significantly reduced the unidirectional fluxes of oxalate and enhanced sodium secretion by decreasing J
ms
Na
. The anion exchange inhibitor 4,4-diisothiocyanatostilbene-2,2-disulfonic acid (DIDS; 0.1 mM, both sides) reduced the unidirectional fluxes of oxalate and chloride. Serosal epinephrine (50 M) stimulated oxalate absorption (21.3±6.3 pmol cm–2 h–1) and sodium absorption (5.71±1.20 equiv cm–2 h–1), whereas dibutyryl-cAMP enhanced oxalate secretion (–43.4±6.9 pmol cm–2 h–1) and stimulated chloride secretion (–7.27 ±0.64 equiv cm–2 h–1). These results indicate that the P2 segment of the proximal colon possesses (a) secretory as well as absorptive capacities, (b) oxalate fluxes that are mediated by pathways involving Na+, Cl–, HCO
3
–
transport and (c) a net oxalate flux that is sensitive to absorptive and secretory stimuli. 相似文献
86.
H. W. Reinhardt G. Kaczmarczyk R. Mohnhaupt B. Simgen 《Pflügers Archiv : European journal of physiology》1981,389(1):9-15
An experimental elevation of left atrial pressure (eLAP ) by means of a reversible mitral stenosis is accompanied with an increase in sodium excretion (UNa—) and arterial blood pressure (by about 20 mm Hg, 2.7 kPa), and by a decrease in plasma renin activity.It is well established that an increase in renal perfusion pressure (Pren) can augment UNa—. Therefore the present study was undertaken to examine whether the eLAP -induced natriuresis was caused by the increased Pren. — Four female beagle dogs were kept under controlled environmental conditions. They received asodium rich diet (14.5 mmol/Na/kg/d). The dogs were chronically instrumented: purse string around the mitral annulus, catheter in the left atrium, carotid loop, pneumatic cuff above the renal arteries, pressure transducer below the renal arteries. Pren was kept constant by means of a digital servofeedback control circuit. The dogs served as their own controls (13 experiments without and 15 experiments with a controlled renal perfusion pressure were performed).After eLAP(+1.0 kPa), UNa— rose from 4.1±2.6 to 10.3±3.9 mol Na/min/kg. If Pren was kept constant, the corresponding values were 4.2±2.8 and 9.3±2.9 mol/min/kg. These data clearly indicate that the atrial natriuresis is not mediated by an augmentation of renal perfusion pressure. Therefore these results support the hypothesis that atrial natriuresis probably is due to an eLAP-induced suppression of the renin-angiotensin-system or other natriuretic mechanisms.Abbreviations ADP
3×20 min After distension period
- AN
Atrial natriuresis
- bw
kg Body weight
- CP
3×20 min Control period
- DP
3×20 min Distension period
- eLAP
kPa Experimental increase of left atrial pressure (during all DP's about +1.0 kPa)
- HR
l/min Heart rate
- LAP
kPa Left atrial pressure
-
n
1
Number of dogs used
-
n
2
Number of experiments (1 expt/day)
-
n
3
Number of collection periods (urine) or number of samples (HR)
- Part
kPa Mean systemic arterial blood pressure (carotid artery)
- Pren
kPa Mean renal perfusion pressure (aorta, below the renal arteries)
- UCI—
mol/min/kg Chloride excretion
- UK—
mol/min/kg Potassium excretion
- UNa—
mol/min/kg Sodium excretion
- Uosm—
osm/min/kg Osmolar excretion
- —
l/min/kg Urine volume
Preliminary parts of this work have been presented in Kiel (Spring meeting of the Deutsche Physiologische Gesellschaft, March 1979) and in Stockholm, Sweden (III. European Colloquium on Renal Physiology, June 1979). 相似文献
87.
J. K. Healy P. A. Fraser J. A. Young 《Pflügers Archiv : European journal of physiology》1976,363(1):69-73
Summary The effect of angiotensin II on nett electrolyte transport by the main duct of the rabbit mandibular gland was investigated in vitro using a perfused duct preparation bathed in a Haemaccel®-nutrient salt solution. In a bath concentration of 4×10–10 M, angiotensin reduced nett absorption of Na+ and Cl– by about 8% and depolarized the transepithelial electrical potential difference (P.D.) by about 13%; the drug had no effect on ductal transport of K+ and HCO
3
–
. In both lower (4×10–11 M) and higher (4×10–9 M) concentrations, angiotensin had qualitatively similar effects. After exposure to the hormone for about 30 min, Na+ transport and P.D. became unstable and gradually fell away towards zero. It is concluded that angiotensin in physiological concentrations has a specific inhibitory effect on Na+ absorption by salivary duct cells which could arise either from a change in the Na+ pump rate or from a conductance change in the apical or basal membrane of the epithelial cell. 相似文献
88.
89.
Andrea Fleig Peter C. Ruben Martin D. Rayner 《Pflügers Archiv : European journal of physiology》1994,427(5-6):399-405
Na currents recorded from inside-out macropatches excised from Xenopus oocytes expressing the subunit of the rat brain Na channel IIA show at least two distinguishable components in their inactivation time course, with time constants differing about tenfold (
h1 = approx. 150 s and
h2 = approx. 2 ms). In excised patches, the inactivation properties of Na currents changed with time, favoring the faster inactivation kinetics. Analysis of the fast and slow current kinetics shows that only the relative magnitudes of
h1 and
h2 components are altered without significant changes in the time constants of activation or inactivation. In addition, voltage dependence of both activation and steady-state inactivation of Na currents are shifted to more negative potentials in patches with predominantly fast inactivation, although reversal potentials and valences remained unaltered. We conclude that the two inactivation modes discerned in this study are conferred by two states of Na channel the interconversion of which are regulated by an as yet unknown mechanism that seems to involve cytosolic factors. 相似文献
90.
A. Nizet A. Dujardin H. Thoumsin J. Thoumsin-Moons 《Pflügers Archiv : European journal of physiology》1973,341(3):209-217
Summary The changes in blood concentration which result in the adjustment of excretion when renal functioning mass is acutely reduced have been investigated by means of paired experiments on isolated dog kidneys. One kidney was perfused with undiluted blood; the other kidney was perfused with blood supplemented with an amount of water and solutes corresponding to the amount retained after the suppression of the contralateral kidney in situ; the response was evaluated from the difference in excretion between the two organs. The results may be summarized as follows: a) the adjustment of the excretion of water, sodium, potassium and urea results from small changes in blood concentration (haematocrit, plasma proteins and solutes), in the absence of specific stimuli of extrarenal origin; b) increased urea concentration is not the major determinant of the readjustment of sodium and water excretion; c) the response is potentiated by high arterial blood pressure; d) if the load of water exceeds the load of sodium, this ion is retained by the kidney even in the presence of an osmotic load of urea; e) the changes in the blood concentrations do not provide an adequate adjustment of the excretion of phosphate; f) increased excretion per nephron results from decreased fractional reabsorption without significant change in glomerular filtration rate. 相似文献