Toshiki Masumizu

Bromocriptine protects mice against 6-hydroxydopamine and scavenges hydroxyl free radicals in vitro

Pretreatment with bromocriptine (5 mg/kg, i.p., 7 days) completely protected against the decrease in mouse striatal dopamine and its metabolites induced by intraventricular injection of 6-hydroxydopamine after intraperitoneal administration of desipramine, but similar pretreatment with L-DOPA/carbidopa (75/7.5 mg/kg, i.p., 7 days) showed only partial protective effect. Furthermore, in an in vitro system that generated.OH from FeSO4-H2O2, bromocriptine dose-dependently reduced the number of .OH radicals. These findings indicate that bromocriptine has a neuroprotective effect against neurotoxins such as 6-hydroxydopamine, probably due, in part, to its hydroxyl radical scavenging activity and inhibiting effect on dopamine turnover rate. This suggests that early introduction of bromocriptine in the therapy of Parkinsons disease may be superior to treatment with L-DOPA alone.

Growth Inhibitory Factor Prevents Neurite Extension and the Death of Cortical Neurons Caused by High Oxygen Exposure through Hydroxyl Radical Scavenging

Growth inhibitory factor (GIF), a brain-specific member of the metallothionein family (MT-III), has been characterized as a inhibitory substance for neurotrophic factors in Alzheimers disease brains. However, the function of GIF, other than the inhibition of neurotrophic factors, remains unknown. We demonstrate here that exogenous GIF prevents neurite extension of cortical neurons in the early period of differentiation and the death of differentiated neurons caused by high oxygen exposure. Down-regulation of GIF in cortical neurons with antisense S-oligonucleotides promoted neuronal death under high oxygen conditions. ESR spin-trapping studies demonstrated that GIF at 2–6 μm scavenged hydroxyl radicals generated by a Fenton-type reaction or the photolysis of hydrogen peroxide much more effectively than the same concentration of metallothionein I+II. GIF did not scavenge either superoxide produced by the xanthine/xanthine oxidase reaction or NO generated from 1-hydroxy-2-oxo-3-(N-methyl-3-aminopropyl)-3-methyl-1-triazene. Moreover, GIF at 40–80 μm inhibited tyrosine nitration by peroxynitrite as efficiently as metallothionein I+II at the same concentration. These results indicate that GIF prevents neurite extension of neurons in the early period of differentiation and supports the survival of differentiated neurons by scavenging hydroxyl radicals.

Protective role of nitric oxide synthase against ischemia-reperfusion injury in guinea pig myocardial mitochondria.

In guinea-pig myocardial mitochondria preparation, lowering the Ca2+ concentration or pH level in the perfusate rapidly elevated the fura-2 Ca2+ signal ([Ca2+]m). Pretreatment with 10(-4) M L-Arg inhibited the rapid [Ca2+]m influx, whereas administration of 10(-4) M L-NAME did not, suggesting some association between nitric oxide (NO*) synthase (NOS) activation and Ca2+ kinetics in mitochondria. Immunoblotting analysis showed that endothelial (e)-NOS was present in mitochondria, but not inducible (i)-NOS or brain (b)-NOS. Electron microscopy observations revealed that the e-NOS antibody-reactive site in the mitochondria was the inner cristae. The production of reactive oxygen species and NO* in isolated mitochondria was detected by the spin trapping technique with electron paramagnetic resonance (EPR) spectrometry. Pretreatment with 10(-5) M S-nitroso-N-acetyl-DL-penicillamine (SNAP) and 10(-5) M 3-[2-Hydroxy-1-(1-methylethyl)-2-nitrosohydrazino]-1-propananin e (NOC 5), which spontaneously generate NO*, completely inhibited the [Ca2+]m uptake. In addition, N-morpholino sydnonimine hydrochloride (SIN-1) (10(-5) M), which simultaneously generates NO* as well as *O2- and peroxynitrite anion (ONOO-), inhibited the increase in [Ca2+]m. ONOO- (3 x 10(-4) M) itself also inhibited this increase. Pretreatment with the *O2(-)-scavenger manganese superoxide dismutase or catalase (200 units/ml) completely inhibited the increase in [Ca2+]m caused by lowering of either the Ca2+ concentration or the pH in the perfusate. These results suggested that the formation of reactive oxygen species promoted the [Ca2+]m influx. The agents that inhibited the [Ca2+]m influx improved contractility even in Langendorff preparations after ischemia. Based on these findings, we concluded that e-NOS exists in mitochondria and that NO* may play an important protective role in reperfusion cardiac injury after ischemia, by inhibiting the Ca2+ influx into mitochondria which are otherwise damaged by *O2-.

Evaluation of superoxide anion radical scavenging activity of shikonin by electron spin resonance

Abstract The scavenging activity of shikonin (SK) for superoxide anion radical (O2⋅−) was evaluated by electron spin resonance (ESR) to clarify the mechanism of the enhancing effect of SK on wound healing and its anti-inflammatory effect. SK quenched O2⋅− in a dose-dependent manner. Values for the O2⋅− scavenging activity of SK were converted to values representing the equivalent activity of superoxide dismutase (SOD) and were termed SOD-like activity values. SK exhibited potent O2⋅− quenching activity and its SOD-like activity was calculated to be about 920 U/mg. These results suggested that the O2⋅− scavenging activity of SK played an important role in enhancing wound healing and in the anti-inflammatory effect of SK. No difference in O2⋅− scavenging activity was observed between SK and its optical isomer alkannin. SK was reduced to SK semiquinone radical by O2⋅−. The SK semiquinone radical may be responsible for the anti-tumor and anti-bacterial effects of SK.

Guanidino compounds generate reactive oxygen species.

Methylguanidine, guanidinoacetic acid and guanidinosuccinic acid are endogenous substances in body tissues. Extremely high levels of these substances are known to be related to the pathogenesis of epilepsy and renal failure such as uremia. In this study it was demonstrated that methylguanidine, guanidinoacetic acid and guanidinosuccinic acid, and arginine generate hydroxyl radicals in aqueous solution. These findings suggest that a high level of guanidino compounds accumulating near or within cells such as neurons (in an epileptogenic focus) or nephrons (in uremic patients) may cause free radical damage leading to these clinical disorders. Arginine may have a similar role in the pathogenesis of hyperarginemia.

Assessment of ESR-CT imaging by comparison with autoradiography for the distribution of a blood-brain-barrier permeable spin probe, MC-PROXYL, to rodent brain

Blood-brain-barrier (BBB)-permeable, 3-methoxycarbonyl-2,2,5,5-tetramethylpyrrolidine-1-yloxy (MC-PROXYL) and BBB-impermeable carbamoyl-PROXYL were used to assess the ESR imaging technique by comparing with autoradiography. For this purpose, spin probes, 14C-labeled at their five-membered ring, [14C]MC-PROXYL and [14C]carbamoyl-PROXYL, were newly synthesized. These probes were i.p. or i.v. injected into rats and autoradiograms were recorded. The autoradiograms of rat head showed that [14C]MC-PROXYL distributed well in the brain compared to [14C]carbamoyl-PROXYL. In vivo ESR spectra and two-dimensional ESR images of isolated rat brain treated with MC- or carbamoyl-PROXYL also indicated the extensive distribution of MC-PROXYL but not carbamoyl-PROXYL in the rat brain. The three-dimensional ESR images of the head of rats and mice were consistent with the fact that MC-PROXYL but not carbamoyl-PROXYL is incorporated into the brain. The ESR-CT images were better for mice than rats. However, the quality of the ESR-CT images was still not satisfactory. Although the resolution and sensitivity of the ESR-CT images were worse than those of the autoradiographic images, the former technique has unique features and advantages; e.g., functional, noninvasive and three-dimensional detection.

Antioxidative Activity of Water Extracts of Lagerstroemia speciosa Leaves

In order to develop naturally occurring antioxidants from edible plants, the antioxidative effect of hot water extracts of Lagerstroemia speciosa leaves, known by the Tagalog name of banaba in the Phillipines, was studied. The content of tannin in banaba extract was 36.8% in dry weight. Banaba extract showed strong antioxidative activity in a linoleic acid autoxidation system. Banaba extract was found to have a potent radical scavenging action on 1,1-diphenyl-2-picrylhydrazyl (DPPH) radicals and superoxide radicals (O(2-) ) generated by a hypoxanthine (HPX)/xanthine oxidase (XOD) system. In vitro lipid peroxidation of rat liver homogenate induced by tert-butyl hydroperoxide (BHP) was inhibited by the addition of banaba extract in a dose-dependent manner. From these results, banaba extract was demonstrated to be useful as an antioxidant or free radical scavenger to protect biological systems against oxidative stress.

ESR demonstration of nitric oxide production from nitroglycerin and sodium nitrite in the blood of rats

Electron spin resonance (ESR) spectra of iron-metal complexes formed by the reaction between nitric oxide (NO) and hemoglobin (Hb), referred to as nitrosylhemoglobin (HB-NO), were observed in rat blood treated in vitro and in vivo with nitroglycerin (GTN) at 77K. The same types of spectra were also detected in rats treated with sodium nitrite (NaNO2). Two types of Hb-NO, which were identified by ESR parameters of g values and superhyperfine coupling constants (shfcc), were the 6- and 5-coordinated complexes. These two types of Hb-NO were generated in a dose-dependent manner in the blood after intraperitoneal administration of 1.5-6 mg of GTN. At the higher dose of GTN (6 mg), the 6-coordinated complex was the major species generated initially, but within 10 min, the 5-coordinated complex increased time-dependently. Quantitative analysis of Hb-NO revealed that when GTN 0.3 mg and 0.6 mg was administered sublingually in rats, the concentration of Hb-NO observed in rat blood was 30% higher than the estimated concentration of GTN. The methemoglobin and peroxide complex of hemoglobin were observed in the blood incubated with GTN at 37 degrees C. These results suggest that the function of GTN was related to oxidative stress with the generation of Hb-NO. Therefore, monitoring of Hb-NO levels may be useful as an indicator of the function of various vasodilators.

Kinetic analysis of the Fenton reaction by ESR‐spin trapping

A quantitative analysis of hydroxyl radical (·OH) generated in the Fe2+‐hydrogen peroxide reaction system was explored by a spin‐trapping method using 5,5‐dimethyl‐1‐pyrroline‐N‐oxide (DMPO) combined with electron spin resonance spectroscopy. Based on the numerical analysis of Fenton‐related reactions, the reduction of DMPO‐OH adduct from 1…n1 stoichiometry prominent at high concentrations of Fe2+ was consistent with a reaction model in which a molar amount of hydrogen peroxide was reduced by two molar amounts of Fe2+. Furthermore, time‐dependent decrease in DMPO‐OH quantity, apparent at much higher concentration of Fe2+, was proved due to the reaction not with Fe2+ but with Fe3+.

Spin trapping for nitric oxide produced in LPS‐treated mouse using various new dithiocarbamate iron complexes having substituted proline and serine moiety

Four dithiocarbamate derivatives of 4‐substituted L‐proline and N‐methyl‐L‐serine were synthesized, and their iron complexes were prepared in Tris‐HCl buffer solution. These complexes were used as spin trapping reagents for nitric oxide in ESR spectrometry, and compared with each other in regard to their spin trapping properties in vivo. When the synthesized complexes were injected to lipopolysaccharide‐treated mice intravenously, the nitric oxide adducts were detected both in the liver and in the blood except N‐dithiocarboxy‐4‐(methoxymethyl)oxy‐L‐proline iron complex, whose nitric oxide adduct was detected mostly in the blood. When the exogenous nitric oxide adduct of this complex was injected, it was not detected in the liver, too. It is considered that this complex can trap nitric oxide in the blood by excluding the accumulation of the nitric oxide adduct in the liver.