ABSTRACT
In this work, pH-sensitive hydrogel nanoparticles based on N-isopropyl acrylamide (NIPAM) and methacrylic acid (MAA) at various molar ratios, were synthesized and characterized in terms of physicochemical and biological properties. FTIR and 1HNMR spectra confirmed the successful synthesis of the copolymer that formed nanoparticles. AFM images and FE-SEM micrographs showed that nanoparticles were spherical, but their round-shape was slightly compromised with MAA content; besides, the size of particles tends to decrease as MAA content increased. The hydrogels nanoparticles also exhibited an interesting pH-sensitivity, displaying changes in its particle size when changes in pH media occurred. Biological characterization results indicate that all the synthesized particles are non-cytotoxic to endothelial cells and hemocompatible, although an increase of MAA content leads to a slight increase in the hemolysis percentage. Therefore, the pH-sensitivity hydrogels may serve as a versatile platform as self-regulated drug delivery systems in response to environmental pH changes.
Subject(s)
Acrylamides/chemical synthesis , Hydrogels/chemical synthesis , Polymethacrylic Acids/chemical synthesis , Acrylamides/chemistry , Acrylamides/pharmacology , Animals , Blood Cells/drug effects , Blood Cells/physiology , Cattle , Cells, Cultured , Freeze Drying , Hemolysis/drug effects , Humans , Hydrogels/chemistry , Hydrogels/pharmacology , Hydrogen-Ion Concentration , Materials Testing , Methacrylates/chemical synthesis , Methacrylates/chemistry , Nanoparticles/chemistry , Particle Size , Polymethacrylic Acids/chemistry , Polymethacrylic Acids/pharmacology , Toxicity TestsABSTRACT
Despite microalgae recently receiving enormous attention as a potential source of biodiesel, their use is still not feasible as an alternative to fossil fuels. Recently, interest in microalgae has focused on the production of bioactive compounds such as polyunsaturated fatty acids (PUFA), which provide microalgae a high added value. Several considerations need to be assessed for optimizing PUFA production from microalgae. Firstly, a microalgae species that produces high PUFA concentrations should be selected, such as Nannochloropsis gaditana, Isochrysis galbana, Phaeodactylum tricornutum, and Crypthecodinium cohnii, with marine species gaining more attention than do freshwater species. Closed cultivation processes, e.g., photobioreactors, are the most appropriate since temperature, pH, and nutrients can be controlled. An airlift column with LEDs or optical fibers to distribute photons into the culture media can be used at small scale to produce inoculum, while tubular and flat panels are used at commercial scale. Depending on the microalgae, a temperature range from 15 to 28Ā Ā°C and a pH from 7 to 8 can be employed. Relevant conditions for PUFA production are medium light irradiances (50-300Ā Āµmol photons m(-2)Ā s(-1)), air enriched with (0-1Ā % (v/v) CO2, as well as nitrogen and phosphorous limitation. For research purposes, the most appropriate medium for PUFA production is Bold's Basal, whereas mixotrophic cultivation using sucrose or glucose as the carbon source has been reported for industrial processes. For cell harvesting, the use of tangential flow membrane filtration or disk stack centrifugation is advisable at commercial scale. Current researches on PUFA extraction have focused on the use of organic solvents assisted with ultrasound or microwaves, supercritical fluids, and electroporation or are enzyme assisted. Commercial-scale extraction involves mainly physical methods such as bead mills and expeller presses. All these factors should be taken into account when choosing a PUFA production system, as discussed in this review.
Subject(s)
Fatty Acids, Unsaturated/isolation & purification , Fatty Acids, Unsaturated/metabolism , Microalgae/growth & development , Microalgae/metabolism , Photobioreactors/microbiology , Culture Media/chemistry , Hydrogen-Ion Concentration , TemperatureABSTRACT
Polymeric blends are employed in the production of filaments for additive manufacturing to balance mechanical and processability properties. The mechanical and thermal properties of polymeric filaments made of poly (lactic acid) (PLA), polyhydroxyalkanoates (PHA), and its blend (PLA-PHA) are investigated herein and correlated to their measured structural and physicochemical properties. PLA exhibits the highest stiffness and tensile strength, but lower toughness. The mechanical properties of the PLA-PHA blend were similar to those of PLA, but with a significantly higher toughness. Despite the lower mechanical properties of neat PHA, incorporating a small amount (12 wt.%) of PHA into PLA significantly enhances toughness (approximately 50%) compared to pure PLA. The synergistic effect is attributed to the spherulitic morphology of blended PHA in PLA, promoting interactions between the amorphous regions of both polymers. Thermal stability is notably improved in the PLA-PHA blend, as determined by thermogravimetric analysis. The blend also exhibits lower cold crystallization and glass transition temperatures as compared to PLA, which is beneficial for additive manufacturing. Following additive manufacturing, X-ray photoelectron spectroscopic showed that the three filaments present an increase in C-C and C=O bonds associated with the loss of C-O bonds. The thermal process induces a slight increase in crystallinity in PHA due to chain reorganization. The study provides insights into the thermal and structural changes occurring during the melting process of additive manufacturing.
ABSTRACT
Polyurethanes are very often used in the cardiovascular field due to their tunable physicochemical properties and acceptable hemocompatibility although they suffer from poor endothelialization. With this in mind, we proposed the synthesis of a family of degradable segmented poly(urea)urethanes (SPUUs) using amino acids (L-arginine, glycine and L-aspartic acid) as chain extenders. These polymers degraded slowly in PBS (pH 7.4) after 24Ā weeks via a gradual decrease in molecular weight. In contrast, accelerated degradation showed higher mass loss under acidic, alkaline and oxidative media. MTT tests on polyurethanes with L-arginine as chain extenders showed no adverse effect on the metabolism of human umbilical vein endothelial cells (HUVECs) indicating the leachables did not provoke any toxic responses. In addition, SPUUs containing L-arginine promoted higher levels of HUVECs adhesion, spreading and viability after 7Ā days compared to the commonly used Tecoflex(Ā®) polyurethane. The biodegradability and HUVEC proliferation on L-arginine-based SPUUs suggests that they can be used in the design of vascular grafts for tissue engineering.
Subject(s)
Arginine/chemistry , Aspartic Acid/chemistry , Glycine/chemistry , Materials Testing , Polyurethanes/chemistry , Polyurethanes/chemical synthesis , Absorbable Implants , Cell Adhesion/drug effects , Cell Proliferation/drug effects , Cells, Cultured , Human Umbilical Vein Endothelial Cells/drug effects , Human Umbilical Vein Endothelial Cells/physiology , Humans , Materials Testing/methods , Models, Biological , Polymers/chemical synthesis , Polymers/chemistry , Polymers/pharmacology , Polyurethanes/pharmacologyABSTRACT
Objective: To evaluate the knowledge, attitudes and behavior regarding antibiotics, use of antibiotics, and antibiotic resistance in students and health care professionals of the district of Barranquilla, Colombia. Study design: Descriptive, cross-sectional. Methods: A sample of 399 respondents was selected, that included health professionals and medical students from 12 health institutions in the district of Barranquilla (Colombia), using an established stratified sampling method. Each of the respondent professionals completed a survey that included 43 items in the Likert scale. A descriptive analysis of the study variables was performed using the software SPSS version 25. Results: Most of the respondents were women (64.4%), aged between 26 and 35 years (47.6%); 28.8% were nurses and 26.1% general practitioners, with ≤10 years of professional experience (63.4%). Overall, the survey revealed that the participants had considerable knowledge about antibiotic use (89.5%-98% correct answers) and the spread of antibiotic resistance (67.4%-89% correct answers). Approximately 74% of the respondents agreed or fully agreed with the questions related to the management of infections and the provision of advice. Conclusions: The present study revealed that most of the health care professionals surveyed had a good knowledge about antibiotic use, although strategies must be developed to strengthen knowledge regarding the spread of antibiotic resistance. Likewise, it is important to identify opportunities for improvement related with access to the guidelines and/or materials necessary to treat infections and to provide advice on antibiotic use and antibiotic resistance.
ABSTRACT
The ammonium exchange capacity of a natural chabazite was studied in this work. The XRD analysis of the zeolite sample revealed that the main zeolitic phase was chabazite. The textural properties were determined by the N(2)-BET method and the surface morphology and charge were examined using a scanning electron microscope and a zetameter, respectively. The ion exchange equilibrium data were obtained in a batch adsorber and the Langmuir isotherm fitted plausibly well the equilibrium data. The effects of the temperature and pH on the ammonium exchange capacity of chabazite were investigated and the capacity increased augmenting the temperature from 15 to 35 Ā°C and pH from 3 to 6. The natural chabazite was modified by a hydrothermal treatment using NaCl and KCl solutions and it was found that the modification influenced the ammonium exchange capacity of the chabazite. The ammonium capacity of natural chabazite was compared with that of a natural clinoptilolite and it was concluded that the chabazite capacity was 1.43 times higher than that of clinoptilolite.
Subject(s)
Quaternary Ammonium Compounds/isolation & purification , Waste Disposal, Fluid/methods , Water Pollutants, Chemical/isolation & purification , Zeolites/chemistry , Hydrogen-Ion Concentration , Ion Exchange , Surface Properties , Temperature , Thermodynamics , X-Ray DiffractionABSTRACT
New polycrystalline SrMo1-xMxO4-ĆĀ“ (M = Fe and Cr) scheelite oxides have been prepared by topotactical oxidation, by annealing in air at 500 Ā°C, from precursor perovskites with the stoichiometry SrMo1-xMxO3-ĆĀ“ (M = Fe and Cr). An excellent reversibility between the oxidized Sr(Mo,M)O4-ĆĀ“ scheelite and the reduced Sr(Mo,M)O3-ĆĀ“ perovskite phase accounts for the excellent behavior of the latter as anode material in solid-oxide fuel cells. A characterization by X-ray powder diffraction (XRD) and neutron powder diffraction (NPD) has been carried out to determine the crystal structure features. The scheelite oxides are tetragonal, space group I41/a (No. 88). The Rietveld-refinement from NPD data at room temperature shows evidence of oxygen vacancies in the structure, due to the introduction of Fe3+/Cr4+ cations in the tetrahedrally-coordinated B sublattice, where Mo is hexavalent. A thermal analysis of the reduced perovskite (SrMo1-xMxO3-ĆĀ“) in oxidizing conditions confirms the oxygen stoichiometry obtained by NPD data; the stability range of the doped oxides, below 400-450 Ā°C, is lower than that for the parent SrMoO3 oxide. The presence of a Mo4+/Mo5+ mixed valence in the reduced SrMo1-xMxO3-ĆĀ“ perovskite oxides confers greater instability against oxidation compared with the parent oxide. Finally, an XPS study confirms the surface oxidation states of Mo, Fe, and Cr in the oxidized samples SrMo0.9Fe0.1O4-ĆĀ“ and SrMo0.8Cr0.2O4-ĆĀ“.
ABSTRACT
Striated muscle contraction is elicited by the release of stored calcium ions through ryanodine receptor channels in the sarcoplasmic reticulum. ryr-1 is a C. elegans ryanodine receptor homologue that is expressed in body-wall muscle cells used for locomotion. Using genetic methods, we show that ryr-1 is the previously identified locus unc-68. First, transposon-induced deletions within ryr-1 are alleles of unc-68. Second, transformation of unc-68 mutants with ryr-1 genomic DNA results in rescue of the Unc phenotype. unc-68 mutants move poorly, exhibiting an incomplete flaccid paralysis, yet have normal muscle ultrastructure. The mutants are insensitive to the paralytic effects of ryanodine, and lack detectable ryanodine-binding activity. The Unc-68 phenotype suggests that ryanodine receptors are not essential for excitation-contraction coupling in nematodes, but act to amplify a (calcium) signal that is sufficient for contraction.
Subject(s)
Caenorhabditis elegans/physiology , Calcium Channels/physiology , Muscle Contraction/physiology , Muscle Proteins/physiology , Ryanodine/metabolism , Animals , Caenorhabditis elegans/genetics , Calcium Channels/genetics , Calcium Channels/metabolism , Chromosome Mapping , DNA Transposable Elements/genetics , DNA, Helminth/genetics , Genes, Helminth/genetics , Microsomes/metabolism , Molecular Sequence Data , Muscle Contraction/drug effects , Muscle Proteins/genetics , Muscle Proteins/metabolism , Muscle, Skeletal/ultrastructure , Mutation , Ryanodine/pharmacology , Ryanodine Receptor Calcium Release ChannelABSTRACT
Airway epithelial chloride secretion is controlled by the apical-membrane chloride permeability. Purified apical-membrane vesicles from bovine tracheal epithelium have now been shown to contain functional chloride channels by using the planar-bilayer technique. Three types of chloride channels were observed; a voltage-dependent, calcium-independent, 71-picoSiemen (in 150 mM NaCl) channel accounted for more than 80 percent of the vesicular chloride conductance and was under strict control of phosphorylation. The channel underwent a fast rundown in less than 2 to 3 minutes of recording, and reactivation required in situ exposure to a phosphorylating "cocktail" containing the catalytic subunit of the adenosine 3',5'-monophosphate (cAMP)-dependent protein kinase. Mean open time and open probability were increased after phosphorylation, whereas slope conductance remained unchanged. Thus, metabolic control of tracheal chloride single channels can now be studied in vitro.
Subject(s)
Chlorides/physiology , Ion Channels/physiology , Membrane Proteins/physiology , Trachea/physiology , Animals , Cattle , Cell Membrane/physiology , Chloride Channels , Chlorides/isolation & purification , Chlorides/metabolism , Electric Conductivity , Membrane Potentials , Membrane Proteins/isolation & purification , Membrane Proteins/metabolism , PhosphorylationABSTRACT
In the sarcoplasmic reticulum membrane of skeletal muscle, the ryanodine receptor forms an aqueous pore identified as the calcium-release pathway that operates during excitation-contraction coupling. The purified ryanodine receptor channel has now been shown to have four properties usually associated with gap junction channels: (i) a large nonspecific voltage-dependent conductance consisting of several open states; (ii) an inhibition of open probability by low pH; (iii) an inhibition of open probability by calcium; and (iv) a sensitivity to blockade by heptanol and octanol but not other alcohols. This functional homology may provide an insight into the mechanism of how muscle cells transduce depolarization into an intracellular release of calcium.
Subject(s)
Intercellular Junctions/physiology , Ion Channels/physiology , Muscles/physiology , Receptors, Cholinergic/physiology , Alcohols/pharmacology , Animals , Electric Conductivity , Ion Channels/drug effects , Kinetics , Membrane Potentials , Receptors, Cholinergic/drug effects , Receptors, Cholinergic/isolation & purification , Ryanodine/metabolism , Ryanodine/pharmacology , Ryanodine Receptor Calcium Release Channel , Sarcoplasmic Reticulum/physiologyABSTRACT
Segmented polyurethanes based on polycaprolactone, 4,4 (metylene-bis-cyclohexyl) isocyanate, and l-lysine were synthesized, manufactured as small vascular grafts and characterized according to ISO 7198 standard for cardiovascular implants-tubular vascular prosthesis. In terms of mechanical properties, the newly synthesized polyurethane films exhibited lower secant modulus than Tecoflex™ SG 80A, a well-known medical grade polyurethane. Similarly, when tested as grafts, the l-lysine-based polyurethane exhibited lower longitudinal failure load (11.5Ć¢ĀĀÆN vs. 116Ć¢ĀĀÆN), lower circumferential failure load per unit length (5.67Ć¢ĀĀÆN/mm vs. 14.0Ć¢ĀĀÆN/mm) and lower suture forces for both nylon (13.3Ć¢ĀĀÆN vs. 24.0Ć¢ĀĀÆN) and silk (14.0Ć¢ĀĀÆN vs. 19.3Ć¢ĀĀÆN) when compared to Tecoflex™ SG 80A grafts. l-Lysine-based graft exhibited a burst strength of 3620Ć¢ĀĀÆmmHg (482.6Ć¢ĀĀÆkPa) and a compliance of 0.16%/mmHg. The cell adhesion was demonstrated with NIH/3T3 fibroblasts where cell adhesion was observed on both films and grafts, while cell alignment was observed only on the grafts. The mechanical properties of this polyurethane and the possibility of strain-induced PCL crystals as the switching phase for shape memory materials, allowed a strain recovery ratio and a strain fixity ratio with values higher than 95% and 90%, respectively, with a repeatability of the shape-memory properties up to 4 thermo-mechanical cycles. Overall, the properties of lysine-based polyurethanes are suitable for large diameter vascular grafts where cell alignment can be controlled by their shape memory potential.
Subject(s)
Blood Vessel Prosthesis , Lysine/pharmacology , Materials Testing , Mechanical Phenomena , Polyurethanes/pharmacology , Animals , Cell Adhesion/drug effects , Fibroblasts/cytology , Fibroblasts/drug effects , Mice , NIH 3T3 Cells , Stress, Mechanical , Tensile StrengthABSTRACT
Angiosarcoma is a deadly neoplasm of the vascular endothelium. Metastatic disease is often present at diagnosis, and 5-year survival is only 10-35%. Although there exist no immunocompetent mouse models of angiosarcoma with which to study immune-based approaches to therapy, angiosarcoma is a major killer of companion dogs, responsible for up to 2% of all canine deaths in some susceptible breeds or an estimated 120,000 per year in the US. The canine disease (HSA) often presents in the spleen as acute hemoabdomen secondary to splenic rupture. Even if life-saving splenectomy is performed, median overall survival (OS) is only 48 days, and 1-year survival is negligible. Here we report the analysis of a pilot phase I open-label trial of chemo-immunotherapy performed on consecutively presenting splenectomized canines with histologically verified HSA. Subjects received an abbreviated course of low-dose doxorubicin plus alpha interferon and an autologous dendritic cell-therapy reported to enhance durable CD8+ memory. Disease was monitored monthly by abdominal ultrasound, chest X-ray, and echocardiogram. Median OS in the per protocol population was 109 days including one of five animals that died cancer-free at 16 months after documented resolution of relapsed disease. These results indicate that therapeutic administration of chemo-immunotherapy is both feasible and safe, substantiating the rationale for additional veterinary and humanĀ clinical studies.
Subject(s)
Cancer Vaccines/immunology , Dendritic Cells/immunology , Dendritic Cells/metabolism , Dog Diseases/immunology , Dog Diseases/therapy , Doxorubicin/pharmacology , Hemangiosarcoma/veterinary , Animals , Cancer Vaccines/administration & dosage , Cells, Cultured , Combined Modality Therapy , Disease Models, Animal , Dog Diseases/diagnosis , Dog Diseases/mortality , Dogs , Female , Immunophenotyping , Immunotherapy , Male , Monte Carlo Method , VaccinationABSTRACT
The release of stored Ca2+ from intracellular pools triggers a variety of important neuronal processes. Physiological and pharmacological evidence has indicated the presence of caffeine-sensitive intracellular pools that are distinct from the well-characterized inositol 1,4,5,-trisphosphate (IP3)-gated pools. Here we report that the brain ryanodine receptor functions as a caffeine- and ryanodine-sensitive Ca2+ release channel that is distinct from the brain IP3 receptor. The brain ryanodine receptor has been purified 6700-fold with no change in [3H]ryanodine binding affinity and shown to be a homotetramer composed of an approximately 500 kd protein subunit, which is identified by anti-peptide antibodies against the skeletal and cardiac muscle ryanodine receptors. Our results demonstrate that the brain ryanodine receptor functions as a caffeine-sensitive Ca2+ release channel and thus is the likely gating mechanism for intracellular caffeine-sensitive Ca2+ pools in neurons.
Subject(s)
Brain/metabolism , Caffeine/pharmacology , Calcium Channels , Calcium/metabolism , Receptors, Cholinergic/physiology , Receptors, Cytoplasmic and Nuclear , Animals , Biophysics/methods , Inositol 1,4,5-Trisphosphate Receptors , Inositol Phosphates/metabolism , Lipid Bilayers , Microscopy, Electron/methods , Rabbits , Receptors, Cell Surface/isolation & purification , Receptors, Cholinergic/isolation & purification , Receptors, Cholinergic/ultrastructure , Ryanodine Receptor Calcium Release ChannelABSTRACT
This study reports the relationship between the biocompatibility and surface properties of experimental bone cements. The effect of hydroxyapatite (HA) or alpha-tri-calcium phosphate (alpha-TCP) incorporated into bone cements prepared with methyl methacrylate as base monomer and either methacrylic acid or diethyl amino ethyl methacrylate (DEAEMA) as comonomers was investigated. The in vitro biocompatibility of these composite cements was assessed in terms of the interaction of primary human osteoblasts grown on the materials over a period of 5 days and compared with a control surface. These results were related to the surface properties investigated through a number of techniques, namely Fourier transform infrared, contact angle measurements, X-ray photoelectron spectroscopy and energy dispersive analysis of X-rays. Complementary techniques of thermal analysis and ion chromatography were also performed. Biocompatibility results showed that the addition of alpha-TCP improves biocompatibility regardless of comonomer type. This is in contrast to HA-based cements where cell proliferation was significantly lower. Surface characterisations showed that structural integrity of the materials was maintained in the presence of the acid and base comonomers, and water contact angles were reduced particularly in DEAEMA containing materials. Furthermore, ion chromatography confirmed higher Ca2+ and PO4(3-) ion release by both types of ceramics, particularly for those containing DEAEMA. In conclusion, the incorporation of acidic and basic comonomers to either HA or alpha-TCP ceramics containing bone cements can have differential effects upon the attachment and proliferation of bone cells in vitro. Moreover, those cements consisting of alpha-TCP and containing DEAEMA comonomer indicated the most favourable biocompatibility.
Subject(s)
Bone Cements/chemistry , Osteoblasts/cytology , Biocompatible Materials , Calcium Phosphates , Cell Division , Ceramics , Durapatite , Humans , Methacrylates , Microscopy, Electron, Scanning , Osteoblasts/ultrastructure , Spectroscopy, Fourier Transform Infrared , Surface Properties , X-RaysABSTRACT
The ion exchange equilibrium of Pb(II) on clinoptilolite modified with NH(4)Cl and NaCl can be represented by two types of isotherms. The first one is the ion exchange isotherm based upon the constant of thermodynamic equilibrium for the ion exchange reaction; however, the fitting procedure for this isotherm can be very tedious due to all the calculations involved and additional thermodynamic data. The second one is the Langmuir isotherm. The use of the Langmuir isotherm to represent ion exchange equilibrium has increased in recent last years since it adequately fits the equilibrium data and, furthermore, its calculation is much simpler. A comparison between the two isotherms showed that they fitted the experimental data reasonably well, but the Langmuir isotherm is much simpler and easier to use.
ABSTRACT
We have studied single-channel conductance for different monovalent cations and streaming potentials caused by osmotic gradients of non-electrolytes in hemocyanin-treated membranes. We have found that the smaller ion, which cannot pass through the channel, is tetramethylammonium and that acetamide is the smaller non-electrolyte excluded from the pore. From the streaming potentials measured, we calculated that no more than three water molecules can accompany the ion through the channel in a row. From these results we conclude that the hemocyanin channel has in its structure a narrow portion which can be represented as a cylinder 6 A long and 5 A in diameter.
Subject(s)
Hemocyanins/physiology , Animals , Ion Channels/physiology , Ion Channels/ultrastructure , Lipid Bilayers , Membrane PotentialsABSTRACT
Functional calcium channels present in purified skeletal muscle transverse tubules were inserted into planar phospholipid bilayers composed of the neutral lipid phosphatidylethanolamine (PE), the negatively charged lipid phosphatidylserine (PS), and mixtures of both. The lengthening of the mean open time and stabilization of single channel fluctuations under constant holding potentials was accomplished by the use of the agonist Bay K8644. It was found that the barium current carried through the channel saturates as a function of the BaCl2 concentration at a maximum current of 0.6 pA (at a holding potential of 0 mV) and a half-saturation value of 40 mM. Under saturation, the slope conductance of the channel is 20 pS at voltages more negative than -50 mV and 13 pS at a holding potential of 0 mV. At barium concentrations above and below the half-saturation point, the open channel currents were independent of the bilayer mole fraction of PS from XPS = 0 (pure PE) to XPS = 1.0 (pure PS). It is shown that in the absence of barium, the calcium channel transports sodium or potassium ions (P Na/PK = 1.4) at saturating rates higher than those for barium alone. The sodium conductance in pure PE bilayers saturates as a function of NaCl concentration, following a curve that can be described as a rectangular hyperbola with a half-saturation value of 200 mM and a maximum conductance of 68 pS (slope conductance at a holding potential of 0 mV). In pure PS bilayers, the sodium conductance is about twice that measured in PE at concentrations below 100 mM NaCl. The maximum channel conductance at high ionic strength is unaffected by the lipid charge. This effect at low ionic strength was analyzed according to J. Bell and C. Miller (1984. Biophysical Journal. 45:279-287) and interpreted as if the conduction pathway of the calcium channel were separated from the bilayer lipid by approximately 20 A. This distance thereby effectively insulates the ion entry to the channel from the bulk of the bilayer lipid surface charge. Current vs. voltage curves measured in NaCl in pure PE and pure PS show that similarly small surface charge effects are present in both inward and outward currents. This suggests that the same conduction insulation is present at both ends of the calcium channel.
Subject(s)
Calcium/metabolism , Ion Channels/metabolism , Lipid Bilayers/immunology , Muscles/metabolism , Phospholipids/immunology , 3-Pyridinecarboxylic acid, 1,4-dihydro-2,6-dimethyl-5-nitro-4-(2-(trifluoromethyl)phenyl)-, Methyl ester , Animals , Barium/metabolism , Electrochemistry , Ion Channels/drug effects , Nifedipine/analogs & derivatives , Nifedipine/pharmacology , Rats , Surface PropertiesABSTRACT
Potassium channels inhibited by adenosine-5'-trisphosphate, K(ATP), found in the transverse tubular membrane of rabbit skeletal muscle were studied using the planar bilayer recording technique. In addition to the single-channel properties of K(ATP) we report its regulation of Mg2+ and by the guanosine-5'-trisphosphate analogue, GTP-y(gamma)-S. The K(ATP) channel (a) has a conductance of 67 pS in 250 mM internal, 50 mM external KCl, and rectifies weakly at holding potentials more positive than 50 mV, (b) is not activated by internal Ca2+ or membrane depolarization, (c) has a permeability ratio PK/PNa greater than 50, and (d) is inhibited by millimolar internal ATP. Activity of K(ATP), measured as open channel probability as a function of time, was unstable at all holding potentials and decreases continuously within a few minutes after a recording is initiated. After a decrease in activity, GTP-y-S (100 microM) added to the internal side reactivated K(ATP) channels but only transiently. In the presence of internal 1 mM Mg2+, GTP-y-S produced a sustained reactivation lasting 20-45 min. Incubation of purified t-tubule vesicles with AlF4 increased the activity of K(ATP) channels, mimicking the effect of GTP-y-S. The effect of AlF4 and the requirement of GTP-y-S plus Mg2+ for sustained channel activation suggests that a nucleotide-binding G protein regulates ATP-sensitive K channels in the t-tuble membrane of rabbit skeletal muscle.
Subject(s)
Adenosine Triphosphate/metabolism , GTP-Binding Proteins/metabolism , Guanosine Triphosphate/metabolism , Muscles/metabolism , Potassium Channels/metabolism , Animals , Rabbits , Time FactorsABSTRACT
A collection of organic cations has been used to probe the gross structural features of the ionic diffusion pathway in a K+-selective channel from sarcoplasmic reticulum (SR). Channels were incorporated into planar phospholipid bilayer membranes, and single-channel currents were measured in the presence of ammonium-derived cations in the aqueous phases. Small monovalent organic cations are able to permeate the channel: the channel conductance drops sharply for cations having molecular cross sections larger than 18-20 A2. Impermeant or poorly permeant cations such as tetraethylammonium, choline, and glucosamine, among others, block K+ conduction through the channel. This block is voltage dependent and can be described by a one-site, one-ion blocking scheme. 19 monovalent organic cations blocks primarily from the trans side of the membrane (the side defined as zero voltage), and much more weakly, if at all, from the cis side (to which SR vesicles are added). These blockers all appear to interact with a site located at 63% (average value) of the electric potential drop measured from the trans side. Furthermore, block by 1,3-bis[tris(hydroxymethyl)-methylamino] propane (BTP) shows that the presence of a blocking ion increases the duration of the apparent open state, as expected for a scheme in which the blocking site can be reached only when the channel is open. The results lead to a picture of the channel containing a wide (at least 50 A2) nonselective trans entry in series with a narrow (20 A2) constriction.
Subject(s)
Cations, Monovalent/pharmacology , Ion Channels/drug effects , Lipid Bilayers/metabolism , Phospholipids/metabolism , Potassium/metabolism , Sarcoplasmic Reticulum/metabolism , Animals , Hydrogen-Ion Concentration , Mammals , Tromethamine/analogs & derivatives , Tromethamine/pharmacologyABSTRACT
The agonist effect of the dihydropyridine (DHP) (-)Bay K 8644 and the inhibitory effects of nine antagonist DHPs were studied at a constant membrane potential of 0 mV in Ca channels of skeletal muscle transverse tubules incorporated into planar lipid bilayers. Four phenylalkylamines (verapamil, D600, D575, and D890) and d-cis-diltiazem were also tested. In Ca channels activated by 1 microM Bay K 8644, the antagonists nifedipine, nitrendipine, PN200-110, nimodipine, and pure enantiomer antagonists (+)nimodipine, (-)nimodipine, (+)Bay K 8644, inhibited activity in the concentration range of 10 nM to 10 microM. Effective doses (ED50) were 2 to 10 times higher when HDPs were added to the internal side than when added to the external side. This sidedness arises from different structure-activity relationships for DHPs on both sides of the Ca channel since the ranking potency of DHPs is PN200-110 greater than (-)nimodipine greater than nifedipine approximately S207-180 on the external side while PN200-110 greater than S207-180 greater than nifedipine approximately (-)nimodipine on the internal side. A comparison of ED50's for inhibition of single channels by DHPs added to the external side and ED50's for displacement of [3H]PN200-110 bound to the DHP receptor, revealed a good quantitative agreement. However, internal ED50's of channels were consistently higher than radioligand binding affinities by up to two orders of magnitude. Evidently, Ca channels of skeletal muscle are functionally coupled to two DHP receptor sites on opposite sides of the membrane.