Palmitate induces ER calcium depletion and apoptosis in mouse podocytes subsequent to mitochondrial oxidative stress.

Pathologic alterations in podocytes lead to failure of an essential component of the glomerular filtration barrier and proteinuria in chronic kidney diseases. Elevated levels of saturated free fatty acid (FFA) are harmful to various tissues, implemented in the progression of diabetes and its complications such as proteinuria in diabetic nephropathy. Here, we investigated the molecular mechanism of palmitate cytotoxicity in cultured mouse podocytes. Incubation with palmitate dose-dependently increased cytosolic and mitochondrial reactive oxygen species, depolarized the mitochondrial membrane potential, impaired ATP synthesis and elicited apoptotic cell death. Palmitate not only evoked mitochondrial fragmentation but also caused marked dilation of the endoplasmic reticulum (ER). Consistently, palmitate upregulated ER stress proteins, oligomerized stromal interaction molecule 1 (STIM1) in the subplasmalemmal ER membrane, abolished the cyclopiazonic acid-induced cytosolic Ca(2+) increase due to depletion of luminal ER Ca(2+). Palmitate-induced ER Ca(2+) depletion and cytotoxicity were blocked by a selective inhibitor of the fatty-acid transporter FAT/CD36. Loss of the ER Ca(2+) pool induced by palmitate was reverted by the phospholipase C (PLC) inhibitor edelfosine. Palmitate-dependent activation of PLC was further demonstrated by following cytosolic translocation of the pleckstrin homology domain of PLC in palmitate-treated podocytes. An inhibitor of diacylglycerol (DAG) kinase, which elevates cytosolic DAG, strongly promoted ER Ca(2+) depletion by low-dose palmitate. GF109203X, a PKC inhibitor, partially prevented palmitate-induced ER Ca(2+) loss. Remarkably, the mitochondrial antioxidant mitoTEMPO inhibited palmitate-induced PLC activation, ER Ca(2+) depletion and cytotoxicity. Palmitate elicited cytoskeletal changes in podocytes and increased albumin permeability, which was also blocked by mitoTEMPO. These data suggest that oxidative stress caused by saturated FFA leads to mitochondrial dysfunction and ER Ca(2+) depletion through FAT/CD36 and PLC signaling, possibly contributing to podocyte injury.

Probiotic characteristics of lactic acid bacteria isolated from kimchi.

AIMS: The present work was aimed at identifying strains of lactic acid bacteria (LAB) from kimchi, with properties suitable for use as starter cultures in yogurt fermentation. METHODS AND RESULTS: A total of 2344 LAB strains were obtained from two different sources, one group consisted of commercial LAB strains from kimchi, and the second group consisted of those strains isolated from various types of kimchi. The LAB strains from both groups were screened for resistance to biological barriers (acid and bile salts), and the four most promising strains were selected. Further analysis revealed that KFRI342 of the four selected strains displayed the greatest ability to reduce the growth of the cancer cells, SNU-C4. The in vivo efficacy of strains in quinone reductase induction assay was evaluated, and the extent of DNA strand breakage in individual cells was investigated using the comet assay. Strain KFRI342 was identified as Lactobacillus acidophilus by 16S rRNA sequence analysis, showed protection against tumour initiation and imparted immunostimulation as well as protection against DNA damage. CONCLUSIONS: Strain KFRI342, which showed probiotic characteristics reducing cancer cell growth, could be a suitable starter culture for yogurt fermentation because of its strong acid production and high acid tolerance. SIGNIFICANCE AND IMPACT OF THE STUDY: This is the first report to describe a bacterium, isolated from kimchi, Lact. acidophilus KFRI342 which has the probiotic characteristics and the acid tolerance needed for its use as a starter culture in yogurt fermentation.

Modulation of N-type Ca2+ currents by A1-adenosine receptor activation in male rat pelvic ganglion neurons.

Modulation of voltage-activated Ca2+ channels by adenosine was investigated in male rat major pelvic ganglion (MPG) neurons by using the whole-cell variant of the patch-clamp technique. Adenosine inhibited high voltage-activated (HVA) Ca2+ currents in a concentration-dependent manner with an EC50 of 313 nM and a maximal inhibition of 36%, respectively. Inhibition of HVA Ca2+ currents in adrenergic and cholinergic MPG neurons was similar. Adenosine did not modulate T-type Ca2+ channels present in adrenergic MPG neurons. Reverse transcription-polymerase chain reaction analysis indicated that MPG neurons express mRNAs encoding A1 and A2a receptors. Ca2+ current inhibition by adenosine was mimicked by N6-cyclopentyladenosine, an A1-selective agonist (EC50 = 63 nM) and prevented by 100 nM 8-cyclopentyl-1,3-dipropylxanthine, an A1-selective antagonist. Conversely, CGS 21680, an A2a-selective agonist, displayed a relatively low potency (EC50 = 2200 nM) for inhibiting Ca2+ currents. The action of adenosine was significantly attenuated by 2 mM guanosine-5'-thiodiphosphate or 500 ng/ml pertussis toxin. The voltage dependence of adenosine-induced current inhibition was evident by 1) a bell-shaped profile between the current inhibition and test potentials, 2) kinetic slowing in the presence of agonist, and 3) relief of the current inhibition by a conditioning prepulse to +80 mV. Finally, 1 microM omega-conotoxin GVIA occluded adenosine-induced current inhibition. Taken together, we concluded that adenosine inhibits N-type Ca2+ currents by activation of A1 receptors via a voltage-dependent and PTX-sensitive pathway in rat MPG neurons. Our data may explain how adenosine acts as an inhibitory modulator of ganglionic and neuromuscular transmission in the pelvic plexus.

ATP-induced [Ca(2+)](i) changes and depolarization in GH3 cells.

Extracellular ATP is a neurotransmitter and mediates a variety of responses. In the endocrine system, there are data suggesting a physiological role for ATP in Ca(2+) signalling and hormone secretion. However, the ATP receptor subtype involved has not been clearly elucidated in GH3 cells, a rat anterior pituitary cell line. BzATP- and ATP-induced [Ca(2+)](i) responses had EC(50) values of 18 and 651 microM, respectively. The maximal response to ATP was only 59+/-8% of that for BzATP. The BzATP-induced [Ca(2+)](i) increase was dependent upon the extracellular Ca(2+) concentration. Preincubation with oxidized ATP (oATP) nearly abolished the ATP- and BzATP-induced [Ca(2+)](i) increases. Both BzATP and ATP induced depolarization in GH3 cells, with EC(50) values of 31 microM and 1 mM, respectively. The maximal depolarization to BzATP and ATP were 152+/-21 and 146+/-16% of that elicited by 30 mM KCl. The rank order of agonist potency for [Ca(2+)](i) and depolarization responses was BzATP > > ATP >2-MeSATP and purine derivatives such as ADP, AMP, adenosine were ineffective. Neither UTP nor alpha, beta-methylene ATP showed any effect. In low-divalent conditions BzATP evoked non-desensitizing inward currents, which were reversed at approximately 0 mV. This nonselective cationic conductance was increased by repeated applications of BzATP and the cells became very permeable to NMDG. Longer applications (30 min) of BzATP stimulated ethidium bromide influx in low divalent conditions, suggesting increased permeability to larger molecules. We also identified the existence of P2X(7) mRNA on GH3 cells by using reverse transcriptase (RT)-polymerase chain reaction (PCR). These results suggest that the GH3 cells have an endogenous P2X(7) receptor and purinergic stimulation may play a potential role in neuroendocrine modulation on these cells.

Effect of cytochalasin B and cycloheximide on the activation rate, chromosome constituent and in vitro development of porcine oocytes following parthenogenetic stimulation.

Activation rate, chromosome constituent and developmental pattern of porcine oocytes was examined in the presence and absence of cytochalasin B and cycloheximide following parthenogenetic stimulation. Treatment with cycloheximide after ethanol or Ca2+ ionophore treatment increased the incidence of activation. The percentage of oocytes with two or more female pronuclei was higher (P < 0.05) in oocytes treated with cytochalasin B than in control or cycloheximide-treated oocytes. Treatment with both electrical stimulation and cytochalasin B increased the incidence of diploid chromosome spreads, and accelerated development to the morula and blastocyst stage compared with the control and cycloheximide-treated groups, suggesting a role of ploidy in the development of parthenote.

Effects of competitive binding on the amperometric determination of copper with electrodes modified with chromotrope 2B.

Electrodes modified with Chromotrope 2B incorporated by ion-exchange into a polycationic film of electropolymerized [Ru(v-bpy)(3)](2+) (v-bpy = 4-vinyl-4'-methyl-2,2'-bipyridyl) have been employed in the amperometric determination of copper in solution and exhibit very high sensitivity as well as linear calibration curves in the concentration range 7 x 10(-8)-1 x 10(-4)M. The effects of competing ligands, including chloride, bromide, oxalate, ammonia, acetate, citrate, borate, humic and fulvic acids, or the presence of competing metal ions such as cobalt or nickel on the uptake of copper by the modified electrodes have also been studied. The presence of competing ligands or metal ions decreases the analytical signal due to copper incorporation. The magnitude of this effect is dependent on the relative strength of coordination of the competing ligands for copper ions or of Chromotrope 2B for the competing metals, and also on the concentration of the interferents. The relevance of this work to speciation studies is discussed.

The bacterial flora of non-carbonated, natural mineral water from the springs to reservoir and glass and plastic bottles.

Quantitative and qualitative determinations of the bacterial flora of non-carbonated natural mineral water at the most important steps during bottling at a large water source yielded the following results: (i) Colony counts (on 1:10 diluted plate count agar, incubated at 20 degrees C for 14 days) for water of the five springs and the mixed water were less than 1 to 4 cfu ml-1. The Gram-negative bacterial flora (n = 50 isolates) showed a very different but constant spring specific species distributions with predominance of either eutrophic fluorescent pseudomonads, oligotrophic non-fluorescent pseudomonads or oligotrophic yellow bacteria. (ii) In the reservoir and immediately after bottling the counts were in the range of 10 cfu ml-1. But nearly 30% of the species of the spring water were no longer detectable and there was a significant increase of Gram-positive bacteria. (iii) After 1 week of storage at 20 degrees C colony counts of more than 10(5) cfu ml-1 were found in plastic bottles, but only about 10(4) cfu ml-1 in glass bottles. Besides, a very distinct change of the composition of the microflora occurred. In glass bottles slow-growing oligotrophic non-fluorescent pseudomonads, yellow bacteria and Acinetobacter predominated. In plastic bottles fast-growing eutrophic and mesotrophic fluorescent pseudomonads, Flexibacter and Acinetobacter were dominating. In mineral water, bottled into thoroughly cleaned glass bottles, colony counts of more than 10(5) cfu ml-1 were found within 4 days. In bottles, cleaned mechanically as usual, the increase was significantly slower with a maximum of only 5 x 10(3) cfu ml-1 after 8 days. The results of inoculation experiments in sterile filtered mineral and distilled water led to the suggestion that the difference between the two types of bottles is caused firstly by an inhibition of growth due to residues of cleaning detergents in the glass bottles. Growth promotion by dissolved organic substances in the plastic bottles only played a minor role. After repairing of the pump at a depth of 300 m in a warm mineral water spring, the colony counts at 20, 37 and 42 degrees C on 1:10 diluted and normal plate count agar increased beyond the limits required by the EC directive for mineral water stored a month. Then colony counts decreased slowly and reached the initial level after 1 year, except for the colony counts 1:10 diluted agar at 20 degrees C which stabilized at a relatively high number and a significant alteration of the microflora.(ABSTRACT TRUNCATED AT 400 WORDS)

A simple nutrient-tolerance (NT) test for the characterization of the different types of oligocarbotolerant and oligocarbophile water bacteria from non-carbonated mineral water.

Comparative determination of the specific growth kinetics in mineral water and low and higher concentrated broths at 20 degrees C of 25 selected Gram-negative bacteria isolated from natural non-carbonated mineral water yielded three groups: (1) facultative oligocarbotolerants--with faster growth in normal broth (In g l-1: yeast extract 2.5; casein peptone 5.0; glucose 1.0); (2) obligate oligocarbotolerants--with equal rates of growth in normal and 1:10 diluted broth; and (3) oligocarbophiles--with faster growth in 1:10 diluted broth and in mineral water. In addition, three nutrient types, 'eu-, meso- and oligotrophic' could be distinguished on the basis of full, weak and no growth in brain-heart infusion broth. Further characterization was made between slow and very slow growth types in 1:10 diluted broth. All 25 isolates were psychrotrophic with a minimum growth temperature below 0 degree C. The optimum and maximum temperatures of growth in 1:10 diluted broth, as determined in a temperature gradient incubator were between 20 and 32, and between 29 and 34 degrees C with an average of 26 and 31 degrees C, respectively. Based on these results a very simple nutrient-tolerance test was proposed. After inoculation of the three media, 1:10 diluted broth, normal broth and brain-heart infusion, it is only necessary to check whether or when visible turbidity occurs during 2 weeks incubation at 20 degrees C. This allows additional characterization of bacteria from natural mineral water, which are often difficult to identify, on the basis of growth characteristics in various types of nutrient media.