Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: UMLS:C0019829 (Hodgkin's disease)
 30,247 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

The normal resting potential of the rabbit lens, -70mV, is altered to -59mV by ouabain concentrations up to 5-1- minus 6M, and to -52mV at 4 degrees C. Ouabain acts only at the anterior lens surface. The temperature effect id completely reversible. The Hodgkin-Katz-Goldman equation can be used with the measured lens potentials and Na+ and K+ levels in the lens and bathing medium to obtain alpha, the ration of the membrane permeabilities to Na+ and K+. The alpha-values obtained were 0.052 at 4 degrees C and 0.053 in 5-10 minus 6M ouabain. These data suggest that the change in potential due to cold and ouabain is caused by an inhibition of an electrogenic Na+ ump in the anterior lens epithelium.
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PMID:An electrogenic component of the potential difference in the rabbit lens. 112 14

Spontaneously beating explanted neonatal rat ventricle cells stop beating and show a steady potential (the mean resting potential, -46.2 mV at 6.0 mM Ko) when exposed to 10 mM Cao or 4 mM Mn. When Ko was increased, resting potential changed only slightly between 3 and 15 mM, but the resting potential versus Ko characteristically approached the slope of a K electrode at high Ko. Elimination of Cl from the medium did not alter the K dependence of the resting potential. However, a hyperpolarization of 9 mV per 10-fold change was observed when Nao was decreased from 50 to 4 mM. Ouabain (10(-4) M) depolarized the membrane within 2 min to a stable level of about -30 mV in spontaneously beating cells and in those treated with Ca channel blockers. This potential was considered as the diffusion component of the membrane potential, Vdiff. Consequently the difference between resting potential and Vdiff represents the ouabain-sensitive or the electrogenic component of the resting potential. Using linearized versions of the Mullins and Noda as well as the Goldman - Hodgkin - Katz equations, we calculated that a PNa/PK between 0.25 and 0.35, a Na/K exchange ratio of 2.0, and a Ki of 160 mM adequately described the K dependence of the resting potential. We demonstrated the contribution of electrogenic Na extrusion to the resting potential of mammalian cardiac cells in culture. Therefore the existence of a composite resting potential precludes the direct comparison of potential measurements obtained under conditions liable to independently modify either the diffusion or the electrogenic component.
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PMID:Diffusion and electrogenic components of the resting potential in explanted neonatal rat ventricle cells. 342 45

The effect of veratridine on the membrane potential of sartorius muscles from Rana pipiens was studied. Membrane potential (Vm) was measured in Ringer solutions containing 2.5, 10, 30, 75, and 190 mM K+ in the absence and presence of veratridine. The product [K]o[Cl]o was kept at 300 mM2 to maintain Donnan equilibrium. External Na+ was lowered to 10 mM. Ouabain (100 microM) was present in all solutions. Vm vs. log [K]o curves were fit using the Goldman-Hodgkin-Katz equation with a single free parameter, alpha = PNa/PK (permeability ratio of Na to K). Veratridine (100 microM) causes alpha to increase 12.6 +/- 1.2-fold (n = 9), from 0.146 to 1.657. The effect of veratridine on Vm is dose dependent and reversible, with a time constant for washout of 40 min. The depolarization produced by veratridine is prevented by tetrodotoxin and by Mg, is sensitive to external Na concentration, and is insensitive to curare.
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PMID:Effect of veratridine on membrane potential of sartorius muscle from Rana pipiens. 609 63

The intracellular sodium ion activity (aiNa), apical membrane potential (psi ac) and apical sodium electrochemical driving force (delta mu Na) in Rana temporaria skin were measured using double-barrelled sodium-sensitive micro-electrodes, in the presence of various apical sodium activities (aoNa), amiloride, ouabain, and during voltage clamp of psi ac. The permeability and specific conductance of the apical cell membrane to sodium entry (PaNa and GaNa respectively) were calculated from the Goldman-Hodgkin-Katz equation and the Nernst-Planck (electrodiffusion) permeability equations respectively. The roles of aoNa and aiNa in the control of apical sodium entry were studied. PaNa increased linearly with log decrease in aoNa between 79 and 0.01 mM. Under short-circuit conditions, aiNa remained constant over the aoNa range of 10-79 mM, but decreased when aoNa was lower than 10 mM, due to a fall in delta mu Na and GaNa. Amiloride decreased PaNa, GaNa and aiNa, a result analogous to that observed in spontaneous low-transporting skins. Ouabain inhibited sodium transport and increased aiNa before any changes in PaNa occurred. The latter decreased only when aiNa rose above 15 mM. Increasing delta mu Na by hyperpolarizing voltage clamp of the apical cell membrane elicited a saturable increase in aiNa. The opposite effect was elicited by depolarizing psi ac. Electrodiffusion appears to be the sole mode of apical sodium entry.
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PMID:Sodium-selective micro-electrode study of apical permeability in frog skin: effects of sodium, amiloride and ouabain. 633 75

The effects of ouabain on passive electrical properties of isolated rabbit atrial muscle fibers (crista-terminalis) were investigated. The space constant as well as the time constant of the crista-terminalis was determined using the partition method of Kamiyama and Matsuda based on the cable equation proposed by Hodgkin and Rushton. Ouabain treatment for 30 minutes at a lower concentration (2 X 10(-7) M), caused no significant change in the space constant and time constant of the crista-terminalis. After ouabain treatment for 30 minutes at a higher concentration (1 X 10(-6) M), the space constant of the crista-terminalis was reduced significantly, whereas the time constant was not affected. An apparent reduction in the resting membrane potential and the amplitude of action potential was also observed at the higher concentration of ouabain. These effects of ouabain on passive electrical properties of the crista-terminalis are most likely explained by the increase of its axial resistance (electrical uncoupling) due to intracellular calcium accumulation resulting from inhibition of the membrane sodium pump. This suggests that such an electrical uncoupling may play an important role in the intra-atrial conduction disturbance by cardiac glycosides.
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PMID:Effect of ouabain on electrical coupling of rabbit atrial muscle fibers. 730 17

Upon microelectrode impalements of the tegument of Echinococcus granulosus protoscoleces incubated in Ringer Krebs solution, electrical potential differences of -49 +/- 1 mV, using procedure I, and -53 +/- 1 mV, using procedure II, were recorded. The changes in the electrical potential difference as well as the structural alterations produced by sodium deoxicholate indicate that the observed potentials are established across the apical membrane of the syncytial tegument. The electrical potential difference is primarily dependent on the K+ gradient across the tegumental membrane: a 10-fold increase in the external K+ causes a 30-mV change in the electrical potential. External Na+ concentration changes also affected the electrical potential difference, but altering the external Cl- has no detectable effect. Amiloride, a very well-known blocker of Na+ epithelia channels, produced a reversible hyperpolarization that reached the maximum response at 10(-3) M. Ouabain, 10(-4) M, caused a depolarization in both fresh and Na-rich protoscoleces, although this depolarization was greater and showed a faster onset under the latter condition. It is concluded that the electrical potential difference of E. granulosus protoscolex is generated at the apical tegumental membrane and that it can be experimentally divided into two main components: One of them depends on ionic gradients and membrane permeabilities in accordance with the electrodiffusion predicted by the Goldman, Hodgkin, and Katz equation, while the other depends on the electrogenicity of an active Na+/K+ transport system.
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PMID:Echinococcus granulosus: characterization of the electrical potential of the syncytial tegument of protoscoleces incubated in vitro--effect of inhibitors. 820 39