Addition Of D-glucose Research Articles

Dietary inulin alters the intestinal absorptive and barrier function of piglet intestine after weaning

An experiment was conducted to study the effects of dietary inulin supplementation on the electrophysiological properties of small intestine of suckling and weaned piglets as indicators for glucose absorption and barrier function. Ten sows were divided into two groups, receiving either a control diet, or a diet with 3% inulin. The diets were fed from 3weeks ante partum to 6weeks post partum. In the first 2weeks of life, piglets received only sow’s milk. Irrespective to sex and without castration of males, four piglets (one piglet of each litter) from each group were selected and sacrificed on day 10 of age. The gastrointestinal tract of each piglet was removed and segments were immediately taken from the mid-jejunum and mounted in Ussing chambers. Furthermore, at weaning (6weeks old) 8 piglets were randomly selected irrespective to sex and males were un-castrated (4 animals from sows received control diet and 4 animals from sows received 3% inulin supplemented diet) and fed for 2weeks either control weaning diet or inulin supplemented diet. Thereafter segments of the mid-jejunum were used to investigate the effect of inulin on the gut electrophysiology of weaned piglets. The increase in short-circuit current (Isc) after the addition of glucose is an indicator of higher glucose absorption and the higher tissue conductance (Gt) of the epithelium suggested a higher intestinal permeability to paracellular Na+. In suckling piglets, the addition of d-glucose on the luminal side of the isolated jejunal mucosa increased (P<0.001) the Isc in the inulin-supplemented and control groups compared to basal values. Electrogenic glucose transport (ΔIsc) was similar in suckling piglets from sows fed inulin or control diet, suggesting that feeding of inulin to the mother sows had no effect on glucose absorption across the jejunal mucosa of suckling piglets. However, the dietary inulin supplementation after weaning increased the ΔIsc (P<0.001) compared with the controls, suggesting that the inulin supplementation increased the electrogenic transport of glucose across the jejunal mucosa of weaned piglets indicating higher glucose absorption. Furthermore, the Gt was higher in the inulin-supplemented weaned piglets than in control piglets, which could be due to the increased paracellular permeability to Na+. In conclusion, dietary inulin increased the glucose transport and altered the intestinal barrier by increasing the intestinal permeability in the jejunal mucosa of post-weaned piglets. Furthermore, the results indicated that inulin has a positive effect on glucose absorption in the piglet small intestine after weaning and subsequently the dietary inulin offers a promising approach to avoid post-weaning gastrointestinal tract disorders in pigs.

Tests for the mechanism of starch biosynthesis: de novo synthesis or an amylogenin primer synthesis

Studies in 1940 on potato phosphorylase reaction with starch found that d-glucopyranose from α-d-glucopyranosyl-1-phosphate was added to the nonreducing-ends of starch chains. This led to the hypothesis that the biosynthesis of starch required a preformed primer. Later it was found that phosphorylase was exclusively a degradative enzyme in vivo and that starch-synthase was the enzyme that reacted with ADPGlc to biosynthesize starch. Amylogenin, a putative self-glycosylated protein, was postulated to be the primer, although it was never demonstrated or found. In the present study, three reactions were performed in sequence with a highly purified potato starch-synthase to determine whether an amylogenin primer was present and required or whether the biosynthesis was de novo. Reaction 1 was performed by adding 2.0mM ADPGlc to synthesize the putative primer to a possible amylogenin in the preparation; in Reaction 2, 10mM ADP-[14C]Glc was added; and in Reaction 3, 10mM nonlabeled ADPGlc was added. After the isolation, reduction, and acid hydrolysis of the products of Reactions 2 and 3, 14C-d-glucitol was obtained from Reaction 2 and was decreased by Reaction 3. The formation of 14C-d-glucitol and its decrease showed that an amylogenin, protein primer was not involved in starch biosynthesis and the synthesis is de novo by the addition of d-glucose to the reducing-ends of growing starch chains.

Fabrication and Characterization of a Thermostable Quinoprotein Aldose Sugar Dehydrogenase Immobilized Electrode

We fabricated a thermostable quinoprotein aldose sugar dehydrogenase (tPQQ-ASD derived from a hyperthermophilic archaeon Pyrobaculum aerophilum) immobilized electrode. The electrode was prepared by immobilizing agarose gel mixed with the enzyme and carbon nanofiber (CNF) on a carbon paste (CP) electrode containing p-benzoquinone (BQ) as an electron mediator. The electrocatalytic response was clearly observed by the addition of D-glucose at the electrode. The electrode properties such as pH, temperature dependency and substrate selectivity basically followed the enzyme properties. The current response against D-glucose increased with measurement temperatures up to 70°C, and response perturbation caused by dissolved oxygen level was not observed at the electrode. As for the results of long-term stability evaluation, the current response was stable for 30 days when the electrode was stored in HEPES buffer solution (pH 7.0) at 4°C.

A Mechanically Controlled Indicator Displacement Assay

Push a host: Mechanical compression was applied to a host monolayer at an interface, which facilitated an indicator displacement assay. The fluorescence resonance energy transfer (FRET) between the host and indicator was switched on by this compression. Addition of D-glucose caused the indicator to be displaced, effectively quenching the FRET process.

De novo biosynthesis of starch chains without a primer and the mechanism for its biosynthesis by potato starch-synthase

The starch-synthase enzymes used in this study were the second acetone precipitate and Fractions 21 and 23, Table 1, [Mukerjea, Ru.; Falconer, D. J.; Yoon, S.-H.; Robyt, J. F. Carbohydr. Res.2010, 345, 1555–1563]. Fractions 21 and 23 had high specific activities of 544 and 944 International Units/mg, respectively. When the enzymes and buffer and substrate were treated with immobilized α-amylase and glucoamylase for 30min, they all had the same activity, before and after treatment, indicating that the enzymes were free of putative primers and synthesized amylose chains de novo, without the addition of primers. Starch-synthase was immobilized and reacted with ADP-[14C]Glc; the immobilized enzyme was removed, washed and treated at pH 2 and 50°C for 30min, giving the release of 14C-d-glucopyranose and 14C-amylose, showing that during catalysis they were covalently attached to the enzyme active-site. Pulse and chase reactions of starch-synthase with ADP-[14C]Glc and ADPGlc, respectively, followed by reduction and acid hydrolysis of the starch-chain product, gave 14C-d-glucitol from the pulse reaction and a significant decrease of 14C-d-glucitol from the chase reaction, showing that the addition of d-glucose from ADPGlc was to the reducing-ends of the growing amylose chains. Reactions of four different concentrations of starch-synthase, with constant ADPGlc concentration and temperature, gave four amylose chains, each with different number average molecular weights that were inversely proportional to the concentration of the enzyme, indicating that the synthesis was processive. From the results, a two catalytic-site, insertion mechanism is proposed for the biosynthesis of starch chains.

Enhanced hydrogen production from biomass via the sulfur redox cycle under hydrothermal conditions

A new method of hydrogen production from biomass via a sulfur redox cycle at moderate temperatures has been proposed. This method, which can utilize excess sulfur from hydrocarbon refining processes and waste or geothermal heat, consists of two half cycles: (1) hydrogen production from an aqueous alkaline solution at subcritical conditions of water, where sulfide, HS − and S 2−, acts as a reducing agent of water, and (2) sulfide regeneration under much milder conditions, with an organic compound derived from biomass acting as a reducing agent of polysulfide, S n 2−, and sulfur oxyanion, S xO y 2−, formed in the first half cycle. During a 60-min reaction of an aqueous sodium sulfide solution, hydrogen production was observed at ≥280 °C and corresponding saturated vapor pressures. Addition of D-glucose, C 6H 12O 6, to the solution after hydrogen production at 300 °C resulted in sulfide regeneration at temperatures ≥60 °C in the present 10-min reaction. Moreover, hydrogen production from glucose via the sulfur redox cycle was demonstrated, where the hydrogen production and sulfide regeneration were conducted at 300 °C and 105 °C, respectively. Results indicated that hydrogen production from 1 mol glucose was greater than that by hydrothermal gasification of glucose at much higher temperatures up to 500 °C.

Hydroxyl distribution in sugar structure and its contributory role in the inhibition of Stachybotrys microspora β-glucosidase (bglG)

Stachybotrys microspora is a filamentous fungus that produces various β-glucosidases, of which two have already been characterized. The present study reports on the production of a third one, named bglG, in the presence of d-glucose used as a sole carbon source, and on its subsequent purification and characterization. Although efficiently produced in the presence of d-glucose, bglG continues to be highly inhibited by this sugar. In fact, the addition of d-glucose significantly decreases the glucose formation rates during the hydrolysis of pNPG. This work reports on the effect of various carbohydrates on bglG activity in order to understand the mechanisms adopted by d-glucose to inhibit this enzyme. The findings indicate that bglG is strongly inhibited by d-glucose (44% of the relative activity at 5mM), d-glucitol (96% of the relative activity), d-mannose (56% of the relative activity), cellobiose and maltose (72% and 71% of the relative activity, respectively). On the other hand, d-galactose, d-fructose, lactose, and sucrose have no effect on bglG activity. Similarly, several isomers, such as 2-acetamido-2-deoxy-d-glucose and 2-deoxy-d-arabino-hexose (2-deoxy-d-glucose) were noted to bring no change on the relative activity of bglG. d-xylose and xylitol, on the other hand, enhanced bglG activity up to 123% and 120% of relative activity, respectively. Accordingly, the configuration, epimerisation, isomerisation, and substitutions played key roles in bglG inhibition. The effect of the combination of iron (the best activator of bglG, 161%) with some of those additives was also investigated. The findings revealed that, while a combination of iron at a concentration of 10mM with d-glucose resulted in a two-fold decrease in bglG inhibition (84% at 5mM), iron maintained the same effect with the remainder of the additives being tested.

Evaluation of the chicory inulin efficacy on ameliorating the intestinal morphology and modulating the intestinal electrophysiological properties in broiler chickens.

Chicory (Cichorium intybus) belongs to plants of the Compositae family accumulating energy in the form of inulin fructan. Chicory, a prebiotic, is a fermentable oligosaccharide and oligofructose that may affect the intestinal mucosal architecture and the electrophysiological parameters. Therefore, this study was conducted to evaluate the effectiveness of adding chicory fructans in feed on the intestinal morphology and electrogenic transport of glucose in broilers. Four hundred, 1-day-old broiler chicks were randomly divided into two groups (200 birds per group) for 5 weeks. The dietary treatments were (i) control, (ii) basal diets supplemented with the dried, ground chicory pulp containing inulin (1 kg of chicory/ton of the starter and grower diets). In duodenum, dietary chicory increased the villus height and villus width and villus height to crypt depth ratio (p< 0.05), but the duodenal crypt depth remained unaffected (p > 0.05). However, in jejunum, the villus height, crypt depth and villus height to crypt depth ratio were decreased by dietary chicory compared with control birds (p < 0.05). In ileum, the villus height and villus crypt depth was decreased by dietary chicory supplementation compared with control (p< 0.05), but, the villus height to crypt depth ratio was increased (p< 0.05). Moreover, dietary chicory relatively affected the electrophysiological parameters of the intestine but did not reach significance. The amount of ΔIsc after d-glucose addition to the jejunal mucosa was numerically higher for chicory fed birds (19 μA/cm(2) ) than control birds (10 μA/cm(2) ). The percentage of increase in the Isc after d-glucose addition (ΔIsc %) was higher for chicory group upto (90%) of the control group. In colon, the actual Isc value and Isc after d-glucose addition was numerically higher for chicory fed birds than control birds (p> 0.05). Moreover, the conductance of jejunal and colonic tissues after d-glucose addition remained unaffected by the dietary chicory. In conclusion, addition of chicory to broilers diet increased the duodenal villus height, villus width and villus height to crypt depth ratio and decreased the villus height and crypt depth in both jejenum and ileum. Furthermore, dietary chicory relatively modified the small intestinal electrogenic transport of glucose in broilers.

Fishing on Living Cells with AFM: Novel Method to Study Topology and Dynamics of Cotransporter SGLT1 Protein

In the apical membrane of epithelial cells from the small intestine and the kidney, the high-affinity Na+/D-glucose cotransporter SGLT1 plays a crucial role in intestinal glucose absorption and in renal glucose reabsorption. Here the over-expression of rabbit SGLT1 in rbSGLT1-transfected Chinese hamster ovary (CHO) cells was first characterized using the immuno-staining method on non-permeabilized cells. The functionality of the SGLT1 was verified by biochemical approaches. Atomic force microscopy (AFM) was employed to probe initial substrate-carrier interactions, topology, and function of SGLT1 in living cells on the single-molecule level. Specific recognition events in force distance cycles were detected using epitope specific antibodies or thio-glucoside bound to the AFM tip. Upon addition of D-glucose or the specific inhibitor phlorizin, binding of antibody primed AFM tips drastically decreased suggesting recognition sites for D-glucose in the extracellular loop 8-9 and for phlorizin in the extracellular loop 13-14. The binding probability of the thio-D-Glucose tip was reduced by various sugars in a potency sequence that differed markedly from transport studies. We therefore propose that the first of several selectivity filters of SGLT1 is formed by the two extracellular loops 8-9 and 13-14. This region undergoes significant conformational changes during sugar translocation. Moreover, the results from the thio-D-glucose coupled via a long heterobifunctional crosslinker with a small end group showed the possibility to observe the D-glucose transport pathway of the SGLT1. These studies demonstrate that AFM is a powerful method to explore the structural and functional dynamics of plasma membrane transport proteins in live cells on a single molecule level.

One-step and large scale synthesis of non-metal doped TiO 2 submicrospheres and their photocatalytic activity

Without using an external precursor a simple and one-step method for the synthesis of C-doped TiO 2 submicrospheres has been developed via hydrolysis of titanium tetraisopropoxide in pure methanol followed by calcination under air at 500 °C. Also, with the addition of d-glucose and NH 4OH solution during the hydrolysis process, C- or N-doped and C, N co-doped TiO 2 submicrospheres can be prepared by the same method. The size of the submicrosphere was homogeneous ranging from 300 to 400 nm. The resulting submicrospheres were characterized by FE-SEM, TEM, XRD, XPS and UV–vis diffuse reflectance spectroscopy. The C- or N-doped and C, N co-doped submicrospheres showed obvious absorption in the wavelength up to around 650, 500 and 650 nm, respectively. The activity of the photocatalysts was evaluated by the hydroxyl radical formation under visible light irradiation. Finally, the mechanism of sphere formation is discussed.

Membrane Permeability in the Gastrointestinal Tract: The Interplay between Microclimate pH and Transporters

Some examples of pH- and transporter-dependent permeability, determined in side-by-side diffusion cells, are summarized. We investigated the polarized transport in the mucosal-to-serosal direction of monocarboxylic acid-type drugs through the excised rat jejunal tissue and an artificial membrane. We established that, in vitro, these substances are most probably not transported by monocarboxylate transporter 1, but by passive pH-dependent transport. We also studied various influences on the permeability of fluorescein, a low permeability marker, through isolated rat intestinal segments, Caco-2 cell monolayers, and an artificial membrane. Polarized transport of fluorescein in the serosal-to-mucosal direction through the rat jejunum by multidrug resistance-associated protein was triggered by the addition of D-glucose to the mucosal side, while the pH-dependent increase of fluorescein influx is presumably the consequence of a monocarboxylate transporter and a member of the organic-anion transporting polypeptide family. With permeability experiments through the excised segments of rat small intestine, we ascertained that ciprofloxacin is a low-permeability drug and has higher and pH-dependent transport in the mucosal-to-serosal direction than in the opposite direction. We also established that neither the permeability of fluoroquinolones nor their solubility in different buffers was influenced by the interactions with metal cations.

Normalization of the live-birth sex ratio after human blastocyst transfer from optimized culture conditions

OBJECTIVE: The addition of D-glucose, when culturing 8-cell cow embryos, increases the male:female sex ratio, but has no effect when added earlier. A meta-analysis of 2,587 offspring demonstrated an increase in male:female sex ratio when transferring blastocysts, but not when transferring cleavage-stage embryos. The objective was to evaluate the live-birth sex ratio resulting from two culture systems.

Cell viability in a wet silica gel

A modified two-step sol–gel route using silicon ethoxide (TEOS) has been used to synthesize amorphous sol–gel-derived silica, which has been successfully used as a cell encapsulation matrix for 3T3 mouse fibroblasts and CRL-2595 epithelial cells due to its non-toxicity. The sol–gel procedure comprised a first, low pH hydrolysis step, followed by a neutral condensation–gelation step. A high water-to-TEOS ratio and the addition of d-glucose as a porogen and source of nutrients were chosen to minimize silica dissolution and improve the biocompatibility of the process. Indeed, the cell integrity in the encapsulation process was preserved by alcohol removal from the starting solution. Cells were then added in a buffered medium, causing rapid gelation and entrapment of the cells within a randomly structured siloxane matrix in the shape of a monolith, which was maintained in the wet state. MTT and alamarBlue assays were used to check the cytotoxicity of the silica gels and the viability of entrapped cells at initial times in contact with silica. To improve cell attachment, cell clumping experiments – where groups of cells were formed – were designed, rendering improved viability. The obtained materials are therefore excellent candidates for designing tissue-culture scaffolds and implantable bioreactors for biomedical applications.

C-terminal Loop 13 of Na+/Glucose Cotransporter 1 Contains Both Stereospecific and Non-stereospecific Sugar Interaction Sites

To investigate whether the C-terminal loop 13 of rabbit sodium/glucose cotransporter SGLT1 is involved in the recognition of the substrate d-glucose, isolated loop 13 (amino acids (aa) 541-638) was immobilized to a lipid bilayer. Interactions were investigated by surface plasmon resonance spectroscopy using an antibody directed against the late part of the loop (aa 606-631) or the glucoside transport inhibitor phlorizin. Specific binding of the antibody to the loop could be detected. The number of bound antibodies decreased upon the addition of d-glucose but not upon the addition of l-glucose. Phlorizin also significantly lowered the number of bound antibodies. Binding of phlorizin to the loop could also be demonstrated directly. Binding of phlorizin was, however, reduced to a similar extent upon the addition of either d-glucose or l-glucose, indicating their unspecific competition with the inhibitor's sugar moiety. Thus, the presence of a stereospecific glucose interaction site in the late part of the loop and a second, but non-stereospecific, sugar binding site on the same loop was assumed. To investigate whether the early part of loop 13 contains this non-stereospecific sugar binding site, peptides containing aa 541-598 were expressed in Escherichia coli and purified. Both d-glucose and l-glucose quenched the peptides tryptophan fluorescence and reduced the Trp accessibility to acrylamide to a similar degree. In view of the recently proposed transmembrane orientation of loop 13, the two binding sites may be part of the extracellular (stereospecific) and intracellular (non-stereospecific) sugar interaction sites of SGLT1.

A nutritional approach for the management of deoxynivalenol (DON) toxicity in the gastrointestinal tract of growing chickens.

It has been shown that DON has negative effects on the active transport of some nutrients in the small intestine of chickens. The plausible interactions between food contaminants and natural components could be high. The present study investigated the effects of DON on the presence or absence of dietary inulin on the electrophysiological response of the gut to glucose. Ussing chamber studies were conducted with isolated jejunal epithelia at the age of 35 days. Electrophysiology of the epithelia was recorded and the changes of the short-circuit current (Isc) were determined. The addition of d-glucose on the luminal side of the isolated mucosa increased (P < 0.05) the Isc in the control group and inulin supplemented group. The oligosaccharides did not increase glucose absorption in young healthy chickens compared with the controls. In the second experiment, after preincubation of tissues with DON, the addition of glucose did not increase the Isc in jejunum and colon in the control group (P > 0.05). However, in the dietary inulin supplemented group in both jejunum and colon, the addition of glucose after preincubation of tissues with DON increased the Isc, suggesting that the dietary inulin supplementation of the broilers regulated and improved the glucose absorption in the presence of DON and kept it at normal levels.

Cyclic AMP post-transcriptionally regulates the biosynthesis of a major bacterial autoinducer to modulate the cell density required to activate quorum sensing

In Vibrio cholerae, expression of the quorum sensing regulator HapR is induced by the accumulation of a major autoinducer synthesized by the activity of CqsA. Here we show that the cAMP–cAMP receptor protein complex regulates cqsA expression at the post-transcriptional level. This conclusion is supported by the analysis of cqsA–lacZ fusions, the ectopic expression of cqsA in Δcrp mutants and by Northern blot analysis showing that cqsA mRNA is unstable in Δcrp and Δcya (adenylate cyclase) mutants. Addition of cAMP to the culture of a Δcya mutant restored cqsA mRNA stability and cholera autoinducer 1 production. Lowering intracellular cAMP levels by addition of d-glucose increased the cell density required to activate HapR. These results indicate that cAMP acts as a quorum modulator.

Starch biosynthesis: experiments on how starch granules grow in vivo

Four varieties of starch granules from potato, wheat, maize, and rice were fractionated into homogeneous 10-μm-sized ranges. The size with the largest amount of granules was reacted with ADP-[ 14C]Glc, washed, and peeled into 7−9 layers, using a controlled peeling process, involving 90:10 volume proportions of Me 2SO–H 2O at 10 °C. All of the starches showed biosynthesis of starch throughout the granules. Starch synthase activities were determined for each of the layers. Three of the starches had a relatively large amount of synthase activity in the second layer, with only a small amount in the first layer. Potato starch had the largest amount of activity in the first layer. Starch synthase activity was found to alternate between higher and lower activities throughout all of the varieties of granules, showing that the synthesis was not uniform and also was not exclusively occurring at the surface of the starch granules, which had previously been hypothesized. From these results and our previous studies on the mechanism of starch chain elongation by the addition of d-glucose to the reducing end of a growing chain that is covalently attached to the active site of starch synthase, a hypothesis is proposed for how starch granules grow in vivo.

Production and Accumulation of Xylooligosaccharides with Long Chains by Growing Culture and Xylanase of a Mutant Strain of Bacillus pumilus X-6-19

Bacillus pumilus X-6-9, isolated from soil and subsequently identified, produced xylooligosaccharides with long chains from xylan and accumulated them in the culture. By improving the culture conditions and mutating the bacterium, a 3.2-fold increase in the production of the xylooligosaccharides was established when compared with the original culture conditions of B. pumilus X-6-19. The addition of D-glucose to the culture of the mutant strain U-3 of B. pumilus X-6-9 repressed the synthesis of β-xylosidase but not xylanase. For these reasons, it was revealed that strain U-3 was a good organism for the production and accumulation of xylooligosaccharides with long chains from xylan by a microbial culture. Xylanase produced by strain U-3 was purified to homogeneity and characterized. The hydrolyzates generated by the purified xylanase contained xylobiose, xylotriose, xylotetraose, and xylopentaose but not xylose.

Sugar response of boronic acid-substituted azobenzene dye-modified polymer

We synthesized a boronic acid-appended azobenzene dye (BA) and attached it to poly(ethyleneimine) (polyBA) for studying its sugar response. The addition of d-glucose induced a significant change in the UV–visible absorption spectra of the polyBA solution. The binding constants for d-glucose ( K glu) and d-fructose ( K fru) were calculated to be 54 M − 1 and 110 M − 1 , respectively. The selectivity for d-glucose was higher in polyBA as compared with that of monomeric BA ( K glu = 1.2 M − 1 , K fru = 17 M − 1 ). We also fabricated multilayered films composed of polyBA and polyanions {poly(vinyl sulfate) (PVS), carboxymethylcellulose (CMC)} using a layer-by-layer deposition technique. In (PVS/polyBA) 10 films, the affinity for d-glucose was relatively low ( K glu = 1.7 M − 1 , K fru = 28 M − 1 ). In contrast, (CMC/polyBA) 5 films showed a high affinity for d-glucose ( K glu = 18 M − 1 , K fru = 42 M − 1 ). The loosely packed structure of the (CMC/polyBA) 5 film and the suitable chemical structures of CMC probably led to a high affinity for d-glucose.

Propofol Restores Brain Microvascular Function Impaired by High Glucose via the Decrease in Oxidative Stress

Vascular dysfunction induced by hyperglycemia has not been studied in cerebral parenchymal circulation. The current study was designed to examine whether high glucose impairs dilation of cerebral parenchymal arterioles via nitric oxide synthase, and whether propofol recovers this vasodilation by reducing superoxide levels in the brain. Cerebral parenchymal arterioles in the rat brain slices were monitored using computer-assisted videomicroscopy. Vasodilation induced by acetylcholine (10 to 10 m) was obtained after the incubation of brain slices for 60 min with any addition of l-glucose (20 mm), d-glucose (20 mm), or propofol (3 x 10 or 10 m) in combination with d-glucose (20 mm). Superoxide production in the brain slice was determined by dihydroethidium (2 x 10 m) fluorescence. Addition of d-glucose, but not l-glucose, reduced arteriolar dilation by acetylcholine, whereas the dilation was abolished by the neuronal nitric oxide synthase inhibitor S-methyl-l-thiocitrulline (10 m). Both propofol and the superoxide dismutase mimetic Tempol (10 m) restored the arteriolar dilation in response to acetylcholine in the brain slice treated with d-glucose. Addition of d-glucose increased superoxide production in the brain slice, whereas propofol, Tempol, and the nicotinamide adenine dinucleotide phosphate (NAD[P]H) oxidase inhibitor apocynin (1 mm) similarly inhibited it. Clinically relevant concentrations of propofol ameliorate neuronal nitric oxide synthase-dependent dilation impaired by high glucose in the cerebral parenchymal arterioles via the effect on superoxide levels. Propofol may be protective against cerebral microvascular malfunction resulting from oxidative stress by acute hyperglycemia.