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J Procopio

Publications and source records attributed to J Procopio.

16 recordsLinked to original sources
PubMed2005

Molecular mechanisms of glutamine action.

Glutamine is the most abundant free amino acid in the body and is known to play a regulatory role in several cell specific processes including metabolism (e.g., oxidative fuel, gluconeogenic precursor, and lipogenic precursor), cell integrity (apoptosis, cell proliferation), protein synthesis, and degradation, contractile protein mass, redox potential, respiratory burst, insulin resistance, insulin secretion, and extracellular matrix (ECM) synthesis. Glutamine has been shown to regulate the expression of many genes related to metabolism, signal transduction, cell defense and repair, and to activate intracellular signaling pathways. Thus, the function of glutamine goes beyond that of a simple metabolic fuel or protein precursor as previously assumed. In this review, we have attempted to identify some of the common mechanisms underlying the regulation of glutamine dependent cellular functions.

Animals↗
PubMed2004

Effects of palmitic acid and cholesterol on proton transport across black lipid membranes.

We studied the effect of palmitic acid (PA) and cholesterol (approximately 17 wt.%) on proton translocation across asolectin (charged) and diphytanoylphosphatidylcholine (DPhPC, neutral) black lipid membranes (BLMs). Potential difference (PD), short circuit current (SCC), and conductance (G(total)) were measured with a digital electrometer. Membranes were exposed to pH gradients (0.4-2.0 units), followed by PA addition to bath (symmetrically, 40-65 microM). The membrane conductive pathway was subdivided into an unspecific and a proton-related routes. A computer program estimated the conductances (G(un) and G(H)) of the two pathways from the measured parameters. No significant differences in proton selectivity were found between DPhPC membranes and DPhPC/cholesterol membranes. By contrast, cholesterol incorporation into asolectin increases membranes selectivity to proton. Cholesterol dramatically reduced G(un) reflecting, probably, its ability of inducing order in lipid chains. In asolectin membranes, PA increases proton selectivity, probably by acting as a proton shuttle according to the model proposed by Kamp and et al. [Biochemistry 34 (1995) 11928]. Cholesterol incorporation into asolectin membranes eliminates the PA-induced increase in proton selectivity. In DPhPC and DPhPC/cholesterol membranes, PA does not affect proton selectivity. These results are discussed in terms of the presence of cardiolipin (CL) in asolectin, cholesterol/PA interactions, and cholesterol order-inducing effects on acyl-chains.

Cell Membrane↗
PubMed2003

Glutamine and glutamate as vital metabolites.

Glucose is widely accepted as the primary nutrient for the maintenance and promotion of cell function. This metabolite leads to production of ATP, NADPH and precursors for the synthesis of macromolecules such as nucleic acids and phospholipids. We propose that, in addition to glucose, the 5-carbon amino acids glutamine and glutamate should be considered to be equally important for maintenance and promotion of cell function. The functions of glutamine/glutamate are many, i.e., they are substrates for protein synthesis, anabolic precursors for muscle growth, they regulate acid-base balance in the kidney, they are substrates for ureagenesis in the liver and for hepatic and renal gluconeogenesis, they act as an oxidative fuel for the intestine and cells of the immune system, provide inter-organ nitrogen transport, and act as precursors of neurotransmitter synthesis, of nucleotide and nucleic acid synthesis and of glutathione production. Many of these functions are interrelated with glucose metabolism. The specialized aspects of glutamine/glutamate metabolism of different glutamine-utilizing cells are discussed in the context of glucose requirements and cell function.

Cell Physiological Phenomena↗
PubMed2000

Fatty acid transport across lipid bilayer planar membranes.

The transport of palmitic acid (PA) across planar lipid bilayer membranes was measured using a high specific activity [14C]palmitate as tracer for PA. An all-glass trans chamber was employed in order to minimize adsorbance of PA onto the surface. Electrically neutral (diphytanoyl phosphatidylcholine) and charged (Azolectin) planar bilayers were maintained at open electric circuit. We found a permeability to PA of (8.8 +/- 1.9) x 10(-6) cm s(-1) (n = 15) in neutral and of (10.3 +/- 2.2) x 10(-6) cm s(-1) (n = 5) in charged bilayers. These values fall within the order of magnitude of those calculated from desorption constants of PA in different vesicular systems. Differences between data obtained from planar and vesicular systems are discussed in terms of the role of solvent, radius of curvature, and pH changes.

Biological Transport↗
PubMed1999

Thioglycolate-elicited rat macrophages exhibit alterations in incorporation and oxidation of fatty acids.

Incorporation and oxidation of fatty acids (FA) were investigated in resident and thioglycolate-elicited (TG-elicited) rat macrophages (Mphi). Both cell types presented a time-dependent incorporation of [14C]-labeled palmitic acid (PA), oleic acid (OA), linoleic acid (LA), and arachidonic acid (AA) up to 6 h. The total amount of [14C]-FA incorporated by resident Mphi after 6 h was: AA > PA = LA > OA. TG-elicited cells presented a 50% reduction in the incorporation of LA, PA, and AA, whereas that of OA remained unchanged as compared to resident Mphi. The FA were oxidized by resident Mphi as follows: LA > OA > PA > AA. TG elicitation promoted a reduction of 42% in LA oxidation and a marked increase in AA oxidation (280%). The increased oxidation of AA in TG-elicited cells may account for the lower production of prostaglandins in Mphi under these conditions. The full significance of these findings for Mphi function, however, remains to be examined.

Animals↗
PubMed1997

Fast and slow voltage modulation of apical Cl- permeability in toad skin at high [K+].

The influence of voltage on the conductance of toad skin was studied to identify the time course of the activation/deactivation dynamics of voltage-dependent Cl- channels located in the apical membrane of mitochondrion-rich cells in this tissue. Positive apical voltage induced an important conductance inhibition which took a few seconds to fully develop and was instantaneously released by pulse inversion to negative voltage, indicating a short-duration memory of the inhibiting factors. Sinusoidal stimulation at 23.4 mM [Cl-] showed hysteresis in the current versus voltage curves, even at very low frequency, suggesting that the rate of voltage application was also relevant for the inhibition/releasing effect to develop. We conclude that the voltage modulation of apical Cl- permeability is essentially a fast process and the apparent slow components of activation/deactivation obtained in the whole skin are a consequence of a gradual voltage build-up across the apical membrane due to voltage sharing between apical and basolateral membranes.

Animals↗
PubMed1996

Effect of oxytocin on transepithelial transport of water and Na+ in distinct ventral regions of frog skin (Rana catesbeiana).

Thoracic, abdominal, and pelvic fragments of ventral skin of Rana catesbeiana were analysed regarding the effect of oxytocin on: (1) transepithelial water transport; (2) short-circuit current; (3) skin conductance and electrical potential difference; (4) Na+ conductance, the electromotive force of the Na+ transport mechanism, and shunt conductance; (5) short-circuit current responses to fast Na+ by K+ replacement in the outer compartment, and (6) epithelial microstructure. Unstimulated water and Na+ permeabilities were low along the ventral skin. Hydrosmotic and natriferic responses to oxytocin increased from thorax to pelvis. Unstimulated Na+ conductance was greater in pelvis than in abdomen, the other electrical parameters being essentially similar in both skin fragments. Contribution of shunt conductance to total skin conductance was higher in abdominal than in pelvic skin. Oxytocininduced increases of total skin conductance, Na+ conductance, and shunt conductance in pelvis were significantly larger than in abdomen. An oscillatory behaviour of the short-circuit current was observed only in oxytocin-treated pelvic skins. Decrease of epithelial thickness and increase of mitochondria-rich cell number were observed from thorax to pelvis. Oxytocin-induced increases of interspaces were more conspicuous in pelvis and abdomen than in thorax.

Animals↗
PubMed1994

Hydraulic analogs as teaching tools for bioelectric potentials.

Hydraulic analogs of bioelectrical potentials are proposed as teaching tools in helping students with no formal background in physics and mathematics. Membrane capacitance is simulated by a water reservoir, V, whose variable level is the membrane potential. Resting membrane potential is simulated by a large capacitance reservoir of fixed level, connected to reservoir V through a tube having the role of the electrical conductance of the membrane. Injection of electrical current into the cell is simulated by injection of water into the membrane capacitance reservoir. Reversal potentials of the end-plate potential are simulated by another water reservoir, with fixed level (analogous to the reversal potential of the end-plate potential) connected to the membrane capacitance reservoir through a tube corresponding to the acetylcholine-activated ion channels. Different phases of the synaptic potential are then described using the hydraulic analogs. Hydraulic analogs have proved, in our experience, to be an efficient tool in complementing the already established electrical equivalents.

Education, Medical↗
PubMed1990

Roles of external and cellular Cl- ions on the activation of an apical electrodiffusional Cl- pathway in toad skin.

This study is concerned with the short-circuit current, Isc, responses of the Cl(-)-transporting cells of toad skin submitted to sudden changes of the external Cl- concentration, [Cl]o. Sudden changes of [Cl]o, carried out under apical membrane depolarization, allowed comparison of the roles of [Cl]o and [Cl]cell on the activation of the apical Cl- pathways. Equilibration of short-circuited skins symmetrically in K-Ringer's solutions of different Cl- concentrations permitted adjustment of [Cl]cell to different levels. For a given Cl- concentration (in the range of 11.7 to 117 mM) on both sides of a depolarized apical membrane, this structure exhibits a high Cl- permeability, P(Cl)apical. On the other hand, for the same range of [Cl]cell but with [Cl]o = 0, P(Cl)apical is reduced to negligible values. These observations indicate that when the apical membrane is depolarized P(Cl)apical is modulated by [Cl]o; in the absence of external Cl- ions, intracellular Cl- is not sufficient to activate P(Cl)apical. Computer simulation shows that the fast Cl- currents induced across the apical membrane by sudden shifts of [Cl]o from a control equilibrium value strictly follow the laws of electrodiffusion. For each experimental group, the computer-generated Isc versus [( Cl]cell - [Cl]o) curve which best fits the experimental data can only be obtained by a unique pair of P(Cl)apical and Rb (resistance of the basolateral membrane), thus allowing the calculation of these parameters. The electrodiffusional behavior of the net Cl- flux across the apical membrane supports the channel nature of the apical Cl- pathways in the Cl(-)-transporting cells. Cl- ions contribute significantly to the overall conductance of the basolateral membrane even in the presence of a high K concentration in the internal solution.

Animals↗
PubMed1988

Comparative roles of voltage and Cl ions upon activation of a Cl conductive pathway in toad skin.

(1) Combined use of external Cl concentration pulses and apical membrane depolarization permitted to compare the roles of apical voltage and Cl ions upon the activation of a skin Cl conductance, GCl, which is assumed to reflect activation of the permeability of a Cl pathway. (2) Apical membrane depolarization induced by skin hyperpolarization, or by short-circuiting skins with high K Ringer's on the inner side, failed to activate GCl in the absence of external Cl, GCl remaining negligible. Under apical membrane depolarization, a step elevation of [Cl]0 slowly activated GCl as characterized by a sigmoidal current response of slow onset concomitant to a slow conductance increase. External Cl removal had the reverse effect, slowly inactivating GCl. (3) With the apical membrane in the normal polarized state, a step increase of [Cl]0 slowly activated GCl to submaximal values. This indicates that the interaction of Cl ions with the apical membrane partially activates GCl in the absence of apical membrane depolarization. (4) Activation of GCl was interpreted on the basis of a direct effect of Cl ions upon the apical membrane, having been attributed to the apical membrane voltage an indirect role. Voltage would affect the Cl distribution across the apical membrane, and, as a result, the Cl concentration at a proposed regulatory site which modulates the apical membrane permeability to Cl ions.

Animals↗
PubMed1988

Chloride transport in amphibian skin: a review.

1. The transport of Cl- ions across amphibian skin is a complex subject since it involves different mechanisms such as electrodiffusion, exchange diffusion and active transport. Cl- translocation occurs predominantly through a transcellular route, the paracellular pathway being of lesser importance. 2. Transcellular Cl- passage takes place mainly through specialized cells, the mitochondria-rich cells. The principal cells of the epithelium, the cells of the stratum granulosum, which handle most of the active transepithelial Na+ transport, have been shown to play an insignificant role in transepithelial Cl- transport. 3. It is accepted that the main limiting barrier to transepithelial Cl- movement is the apical membrane of the outermost epithelial cells. The apical membrane of the mitochondria-rich cells seems to be the site of a Cl- permeability which is modulated by voltage and Cl- ions.

Animals↗
PubMed1982

A quartz cell for studying planar lipid bilayer membranes.

A quartz chamber is proposed for use in experiments with planar lipid bilayer membranes. Membranes are formed in a hole made on the lateral wall of a fused quartz test tube, immersed in an electrolyte solution. The quartz cell is easy to clean, chemically inert and easily made. Membranes formed in this chamber had specific resistances higher than 10(8) omega.cm2 and excellent mechanical stability.

Lipid Bilayers↗
PubMed1980

Ion movement through gramicidin A channels. On the importance of the aqueous diffusion resistance and ion-water interactions.

The movement of an ion through a membrane channel proceeds in at least five separate steps: Diffusion through the aqueous phases up to the channel, association with the channel itself, translocation through the channel, dissociation from the channel, and diffusion through the aqueous phases out from the channel. We demonstrate that, contrary to current working assumptions, the aqueous diffusion step may be an important determinant of overall ion movement through the channel. We further describe the kinetics of Na+ movement through gramicidin A channels. Using these data we show that one will have to consider the movement of H2O through the channel explicitly in any complete model for ion translocation through the channel interior.

Cell Membrane Permeability↗
PubMedDate not supplied

Glutamine-dependent changes in gene expression and protein activity.

The functions of glutamine are many and include, substrate for protein synthesis, anabolic precursor for muscle growth, acid-base balance in the kidney, substrate for ureogenesis in the liver, substrate for hepatic and renal gluconeogenesis, an oxidative fuel for intestine and cells of the immune system, inter-organ nitrogen transport, precursor for neurotransmitter synthesis, precursor for nucleotide and nucleic acid synthesis and precursor for glutathione production. In the present review information on the mechanism of glutamine action is presented. This amino acid has been shown to regulate the expression of several genes (such as p47phox, p22phox, gp91phox, alpha-actin and fibronectin) and activate several proteins (such as ASK1, c-myc, c-jun and p70s6k).

Animals↗