gramicidin-a and 3-3--dihexyl-2-2--oxacarbocyanine

gramicidin-a has been researched along with 3-3--dihexyl-2-2--oxacarbocyanine* in 4 studies

Other Studies

4 other study(ies) available for gramicidin-a and 3-3--dihexyl-2-2--oxacarbocyanine

ArticleYear
Depolarization of the membrane potential by beta-lactams as a signal to induce autolysis.
    Biochemical and biophysical research communications, 2002, Feb-01, Volume: 290, Issue:4

    The effect of beta-lactam antibiotics that are known to inhibit cell wall biosynthesis and induce cell wall autolysis on the electrophysiological state of the plasma membrane in Streptomyces griseus was studied. Addition of various beta-lactam antibiotics induced a dose- and growth-stage-dependent depolarization of the membrane potential of Streptomyces griseus. The hydrolyzed biologically inactive derivative penicilloic acid had no depolarizing effect on the membrane potential. The ionophore gramicidin D, while depolarizing the membrane potential, also induced a dose-dependent increase in cell wall lysis. These observations suggest that alteration of the transmembrane potential could be an important signal in triggering cell wall autolysis of S. griseus.

    Topics: Anti-Bacterial Agents; Autolysis; Carbocyanines; Cefotaxime; Coloring Agents; Drug Interactions; Gramicidin; Ionophores; Membrane Potentials; Penicillin G; Streptomyces griseus

2002
Membrane potential changes after infection of monocytes by Toxoplasma gondii.
    International journal for parasitology, 2001, Volume: 31, Issue:10

    Membrane potential changes in host cell plasma membrane were analyzed and the parasitophorous vacuole membrane (PVM) potential was characterized after infection by Toxoplasma gondii. Human monocytes infested by T. gondii were stained with two membrane potential sensitive dyes, DiOC(6)(3) carbocyanine and DiSBAC(2)(3) bis-oxonol, before fluorescence emission analysis by confocal laser scanning microscopy. After 24 and 48 h of infection, 34 and 39%, respectively, of monocytes showed several parasites (from two to six) per cell. At these infection times, significant decreases in cytoplasmic emissions were observed for both DiOC(6)(3) and DiSBAC(2)(3). Thus, hyperpolarisation of the host plasma membrane would occur consecutively to infection. Inside the parasitophorous vacuole, the fluorescence intensity of DiOC(6)(3) and DiSBAC(2)(3) increased significantly from 6 to 24 h after infection and the PVM became less polarised. Involvement of different ATPases in the membrane potential of infected monocytes was evaluated with ouabain, DCCD, omeprazole and sodium orthovanadate, ATPase inhibitors. All inhibitors induced a depolarisation of the plasma membrane. In the parasitophorous vacuole compartment, DCCD, omeprazole and sodium orthovanadate but not ouabain caused a significant depolarisation of the PVM, suggesting that H(+), H(+)/K(+) and P-type ATPases were at the origin of the PVM potential. This is the first report showing the presence of ion transporters in the T. gondii PVM and the existence of at least two members of the P-type family of ion pumps: an electrogenic H(+)ATPase and an electroneutral H(+)/K(+) ATPase.

    Topics: Adenosine Triphosphatases; Animals; Carbocyanines; Cell Membrane; Dicyclohexylcarbodiimide; Enzyme Inhibitors; Gramicidin; Humans; Membrane Potentials; Microscopy, Confocal; Microscopy, Fluorescence; Monocytes; Omeprazole; Ouabain; Toxoplasma; Vanadates

2001
Flow cytometric detection of fluorescent redistributional dyes for measurement of cell transmembrane potential.
    Methods in molecular biology (Clifton, N.J.), 1998, Volume: 91

    Topics: Carbocyanines; Cell Membrane; Cell Survival; Flow Cytometry; Fluorescent Dyes; Gramicidin; Humans; In Vitro Techniques; Indicators and Reagents; Leukocytes, Mononuclear; Membrane Potentials; Models, Biological; Valinomycin

1998
Flow cytometric estimation of transmembrane potential of macrophages--a comparison with microelectrode measurements.
    Cytometry, 1986, Volume: 7, Issue:4

    Potential-dependent accumulation of the lipophilic cationic dye 3,3' dihexyloxacarbocyanine (DiOC6(3)) in macrophages has been investigated. Resulting fluorescence of cells was measured by flow cytometry. Alterations of membrane potential of macrophages were induced by ionophore treatment (valinomycin and gramicidin) in a dose-dependent (10(-5) M-10(-7) M) and time-dependent (0 min-45 min) manner. Resulting changes in relative fluorescence intensity were compared with changes of transmembrane potential measured by intracellular recordings obtained by applying glass microelectrodes. The comparative studies offer the possibility to calibrate the flow cytometric estimate of membrane potential of suspended cells. Equilibration of dye partition between cells and surrounding medium is strictly potential-dependent at dye concentrations between 5 X 10(-8) M and 10(-7) M and within an incubation interval from 10 min up to 30 min after addition of dye. Conclusions are drawn concerning the field of application of the optical method. Dynamics of electrical processes following ionophore treatment are discussed in terms of molecular mechanisms of altered ionic transport.

    Topics: Animals; Carbocyanines; Flow Cytometry; Gramicidin; Guinea Pigs; Kinetics; Macrophages; Membrane Potentials; Microelectrodes; Valinomycin

1986