Literature DB >> 2457454

Dopamine accumulation in large unilamellar vesicle systems induced by transmembrane ion gradients.

M B Bally1, L D Mayer, H Loughrey, T Redelmeier, T D Madden, K Wong, P R Harrigan, M J Hope, P R Cullis.   

Abstract

Transmembrane movement of dopamine in response to K+ or H+ ion gradients has been investigated. It is shown that dopamine can accumulate rapidly into large unilamellar vesicles (LUVs) composed of egg phosphatidylcholine exhibiting either a K+ diffusion potential (delta psi; negative inside) or a pH gradient (inside acidic). This can result in entrapped dopamine concentrations of 30-40 mM and inside-outside concentration gradients of nearly 300-fold. The transmembrane dopamine gradients formed in LUV systems exhibiting delta pH (inside acidic) indicate that the transport process can be dictated by movement of the neutral form of dopamine which redistributes according to a simple Henderson-Hasselbach equilibrium. The mechanism of dopamine transport in response to a valinomycin-induced K+ potential is more complex. Although generation of a K+ diffusion potential results in acidification of the vesicle interior, the magnitude of the induced delta pH (approx. 1 pH unit) is insufficient to account for the dopamine concentration gradient achieved (greater than 200-fold). Further, data presented here suggest that higher uptake levels of dopamine can be achieved when certain anions (ATP and citrate) are entrapped within the LUV system. These anions may complex with the protonated form of dopamine creating a non-equilibrium trapping phenomena resulting in interior concentrations of dopamine in excess of that predicted by a simple Henderson-Hasselbach equilibrium.

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Year:  1988        PMID: 2457454     DOI: 10.1016/0009-3084(88)90078-3

Source DB:  PubMed          Journal:  Chem Phys Lipids        ISSN: 0009-3084            Impact factor:   3.329


  11 in total

1.  Transmembrane distribution of lipophilic cations in response to an electrochemical potential in reconstituted cytochrome c oxidase vesicles and in vesicles exhibiting a potassium ion diffusion potential.

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4.  Ion gradient-induced membrane translocation of model peptides.

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Journal:  Biophys J       Date:  1991-09       Impact factor: 4.033

Review 5.  Treating relapsed or refractory Philadelphia chromosome-negative acute lymphoblastic leukemia: liposome-encapsulated vincristine.

Authors:  Tyler Davis; Sherif S Farag
Journal:  Int J Nanomedicine       Date:  2013-09-16

Review 6.  Artificial Lipid Membranes: Past, Present, and Future.

Authors:  Christina G Siontorou; Georgia-Paraskevi Nikoleli; Dimitrios P Nikolelis; Stefanos K Karapetis
Journal:  Membranes (Basel)       Date:  2017-07-26

7.  Spectroscopic studies of D-alpha-tocopherol concentration-induced transformation in egg phosphatidylcholine vesicles.

Authors:  Krzysztof Dwiecki; Paweł Górnas; Agnieszka Wilk; Małgorzata Nogala-Kałucka; Krzysztof Polewski
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8.  Exosomal delivery of doxorubicin enables rapid cell entry and enhanced in vitro potency.

Authors:  Christina Schindler; Andie Collinson; Carl Matthews; Amy Pointon; Lesley Jenkinson; Ralph R Minter; Tristan J Vaughan; Natalie J Tigue
Journal:  PLoS One       Date:  2019-03-29       Impact factor: 3.240

9.  PEG-polypeptide block copolymers as pH-responsive endosome-solubilizing drug nanocarriers.

Authors:  Mohiuddin A Quadir; Stephen W Morton; Zhou J Deng; Kevin E Shopsowitz; Ryan P Murphy; Thomas H Epps; Paula T Hammond
Journal:  Mol Pharm       Date:  2014-06-12       Impact factor: 4.939

Review 10.  Development and Characterization of the Solvent-Assisted Active Loading Technology (SALT) for Liposomal Loading of Poorly Water-Soluble Compounds.

Authors:  Griffin Pauli; Wei-Lun Tang; Shyh-Dar Li
Journal:  Pharmaceutics       Date:  2019-09-09       Impact factor: 6.321

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