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H Hirata

Publications and source records attributed to H Hirata.

At least 145 records · Page 8Linked to original sources

A novel long-latency response of locus coeruleus neurons to noxious stimuli: mediation by peripheral C-fibers.

1. Extracellular recordings were obtained from single presumed noradrenergic neurons in the nucleus locus coeruleus (LC) in response to percutaneous electrical foot shock (FS) stimulation in the rat. We employed long-duration stimulus pulses to examine the possible contribution of peripheral C-fibers to evoked activity in LC. 2. As in previous studies, 0.5-ms FS stimuli produced a short-latency excitatory response (onset 20.8 ms) followed by a prolonged postactivation inhibition. However, 2.0- or 5.0-ms FS stimuli yielded an additional late excitatory response. 3. The onset and termination latency of this late excitatory response were approximately 200 and 400 ms, respectively, after the FS. The conduction velocity for this late response (peripheral plus central pathway) was estimated to be < 1.2 m/s. 4. The percentages of LC neurons that exhibited a significant late response was 4% (3/85) with 0.5-ms stimuli, 53% (31/59) with 2.0-ms stimuli, and 73% (47/64) with 5.0-ms FS stimuli. 5. The average number of spikes evoked per FS stimulus (presented at 0.5 Hz) increased from the 1st to the 21st FS stimulus. This increased response occurred selectively in the late, not in the early, response. This result was interpreted to represent a "windup" phenomenon reflected at the level of LC. 6. Direct application of capsaicin onto the sciatic nerve reduced the average magnitude of the late response of LC neurons to 17% of control 42.5 min after application. The magnitude of the short-latency response components showed little or no change. 7. Averaged compound action potential (cAP) recordings from the sciatic nerve revealed that C-fiber responses were more consistently observed and much larger with 5.0-ms compared with 0.5-ms FS stimuli. 8. C-fiber cAPs were reduced or eliminated after application of capsaicin distal to the recording site with a time course similar to that of the late response of LC neurons, with little or no effect on A-fiber cAPs. 9. These data show that a previously undescribed long-latency response of LC neurons to noxious FS stimulation in rat results from C-fiber activation in the sciatic nerve. This late response may be involved in generating descending noradrenergic analgesia induced by electrical stimulation of the foot pad or other body regions. Future studies of the pharmacology of this late response to noxious stimuli in LC may aid in developing new therapies for the treatment of acute or chronic pain.

Animals↗

A case of oncocytoma in the eyelid.

Oncocytoma rarely arises from the eyelid and only 2 cases have been reported previously. We present a case of oncocytoma in the upper eyelid around the lacrimal punctum. Anatomical location and histological findings suggested that oncocytes of this tumor originated from the epithelium of Moll's gland or the lacrimal canaliculus.

Adenoma, Oxyphilic↗

Immunohistological studies of an oncocytoma.

An oncocytoma of the upper eyelid that occurred in an 82-year-old male was studied immunohistologically according to the avidin-biotin-peroxidase complex method (secretory component, carbohydrate antigen 19-9, carcinoembryonic antigen, anticytokeratin AE1/AE3, S-100 protein, myoglobin, actin, vimentin). The staining properties of columnar-type oncocytes were the same as those of epithelial cells of excretory ducts of Moll's gland, but those of polygonal-type oncocytes were similar to those of myoepithelial cells of Moll's gland. Our results suggested that excretory duct epithelial cells of Moll's gland are the origin of oncocytoma of the eyelid.

Adenoma, Oxyphilic↗

Influence of efonidipine hydrochloride, calcium antagonist on the epithelium of prostates in spontaneously hypertensive rats.

The hypertensive effect on the development of the prostatic abnormality in spontaneously hypertensive rats (SHRs) was examined using Efonidipine hydrochloride, a calcium antagonist. The control SHRs were given a high sodium and potassium diet (SP-diet) alone, and the treated SHRs were given a SP-diet with 0.15% Efonidipine hydrochloride from 8 to 28 weeks of age. The systolic blood pressure (SBP) in the control SHRs increased with age, while the elevation of SBP was significantly prevented in the treated SHRs. Light-microscopically, the prostatic lesion was observed both in the control and treated SHRs. The glandular lumen was narrowed with papillary protrusions, and the epithelium was composed of tall columnar epithelial cells. However, hypertension-induced complications in kidneys and hearts were not observed in the treated SHRs. These results suggested that the prostatic abnormality of SHRs might not be the consequent lesions upon hypertension.

Animals↗

Regional changes in alpha-tubulin and beta-actin mRNA accumulations after transient ischemia in spontaneously hypertensive rat brains.

Regional changes in the mRNA accumulations for cytoskeletal proteins alpha-tubulin and beta-actin were examined by in situ hybridization and Northern blot analysis in spontaneously hypertensive rat brains at chronic stages after 3 hours of transient ischemia. alpha-Tubulin mRNA accumulations showed no significant change at 2 weeks after transient ischemia except for a significant decrease in the frontal cortex (9.7%, p < 0.01) coinciding with ischemia induced histological changes. beta-Actin mRNA level was significantly increased in the parietal cortex (8.5%), septum (10.0%), amygdala (11.0%), CA4 area (5.8%) and the dentate gyrus (7.5%) of the hippocampus at 2 weeks after recirculation compared with a sham-operated control group (p < 0.01). The ischemic areas of hippocampal and frontocortical lesions receive afferent neurons from those regions where beta-actin mRNA was increased, suggesting that ischemia-induced increases in beta-actin mRNA may reflect actin synthesis in these neurons to compensate for lost synaptic connections. Two cytoskeletal mRNA concentrations reacted differently to cerebral ischemia, and did not parallel histological signs of ischemia either temporally or spatially.

Actins↗

Histological findings of capsular delamination of the lens.

Histological findings in a 75-year-old man with idiopathic capsular delamination were reported. The anterior capsules were obtained during extracapsular cataract extraction, and examined by light and electron microscope. The epithelial side of the anterior capsules protruded towards the anterior chamber at the edge of the delaminated areas. This finding has not been described previously, and the defect in this fragile region was thought to be the cause of capsular delamination.

Aged↗

[The effects of transcorneal administration of prostaglandin E2 on rabbit eyes].

The pharmacologic effects of prostaglandin E2 (PGE2) on the anterior ocular segment were investigated. PGE2 was administered with a glass cylinder attached to the cornea in concentrations ranging from 0.05 to 500 micrograms/ml. The intraocular inflammatory reaction was assessed according to the changes in the anterior chamber flare, ocular tension, and components of the aqueous humor. We also performed experiments designed to inhibit the reactions induced by PGE2 using anti-inflammatory agents. The PGE2 elicited a single peak reaction in the anterior chamber flare, which recovered after several hours, and a transient elevation in the ocular tension in the early stage after PGE2 administration. Quantitative analysis of these two reactions revealed that both were dependent on the dose of PGE2 administered. The concentrations of ascorbic acid and glutathione, particularly that of the reduced form of the latter, were transiently reduced in the aqueous humor. The anterior chamber flares were suppressed by agents that inhibit arachdonic acid metabolism. These findings suggest that the metabolism of arachdonic acid becomes newly activated as a result of stimulation by PGE2 of extrinsic origin.

Animals↗

[The effects of calcium antagonists on prostaglandin E2 reaction in rabbit eyes].

We determined the effects of calcium antagonists (CAs) on prostaglandin E2 (PGE2) induced responses in the anterior ocular segment. PGE2 was administered to pigmented rabbit eyes with a glass cylinder attached to the corneal surface. CAs (nicardipine, verapamil, diltiazem: 125-1,000 micrograms/kg) were injected intravenously either once (30 min. before or at the same time as the PGE2 administration), or twice (at the same time as the PGE2 administration and 30 min. after). We evaluated the aqueous flare (AF) for 6 hours using a laser flare cell meter and intraocular pressure (IOP). A single peak rise of AF was observed about 1 hour after the PGE2 administration and a transient elevation of IOP 15-30 min. after. Intravenously injected CAs reduced these responses. Nicardipine (500-1,000 micrograms/kg) in particular significantly suppressed both the rise of AF and the IOP elevation. These results suggest that CAs suppress ocular inflammatory responses induced by PGE2 effectively.

Animals↗

Alteration of renal receptors for atrial natriuretic peptide and vasopressin in spontaneously hypertensive rats treated with antihypertensive diuretics.

To investigate the alteration of the renal atrial natriuretic peptide (ANP) and arginine vasopressin (AVP) receptors in the controlled hypertensive state of spontaneously hypertensive rat (SHR) treated with antihypertensive diuretics, 12 weeks old SHRs were administered an antihypertensive diuretic, furosemide, trichloromethiazide, or indapamide, daily for 10 days and investigated by radiolabeled receptor assay (RRA) of ANP and AVP. The urine volume was significantly increased in all groups treated with antihypertensive diuretics as compared with the untreated control group on day 3. Systolic blood pressure was significantly decreased in groups treated with both trichloromethiazide and indapamide. The number of renal ANP receptors decreased; affinity was increased only in the SHR administered indapamide. The affinity of the renal AVP receptor was also decreased in that group. Alteration of ANP and AVP receptors was observed only in the group treated with indapamide. This indicates that the ANP and AVP receptor in the kidney of SHR was changed not only by diuresis or reduction of blood pressure, but by the pharmacological action of indapamide.

Animals↗

Depth-dependent change in membrane fluidity by phenolic compounds in bovine platelets and its relationship with their effects on aggregation and adenylate cyclase activity.

The effects of phenolic compounds on membrane fluidity of bovine blood platelets were investigated by studies on the fluorescence anisotropies of diphenylhexatriene (DPH) and its ionic derivatives to clarify the relationship of these effects with the inhibitory effects of the compounds on aggregation. Among the phenolic compounds tested, monohydric phenols (phenol and two monosubstituted derivatives) decreased the fluorescence anisotropy of DPH, which is thought to be located within the hydrophobic core of the membrane, in concentration ranges in which they inhibited platelet aggregation. On the other hand, they had little or no effects on the fluorescence anisotropies of the ionic derivatives of DPH, which are thought to be located in the interfacial region of the lipid bilayer. Consistent with their effects on the fluorescence anisotropy of DPH, these monohydric phenols increased the intracellular cAMP concentration. Thus, these monohydric phenols may inhibit platelet function by stimulation of adenylate cyclase mediated by perturbation of the central region of the membrane lipid bilayer. On the other hand, pyrocatechol and pyrogallol, which have two and three phenolic hydroxyl groups and have much larger electron donor activities than the monohydric phenols tested, inhibited platelet function by a different mechanism, because they did not cause increase in either membrane fluidity or the cAMP concentration of platelets.

Animals↗

Solubilization and reconstitution of high- and low-affinity Na(+)-dependent neutral L-alpha-amino acid transporters from rabbit small intestine.

High- and low-affinity Na(+)-dependent neutral L-alpha-amino acid transporters were solubilized with 0.25% octaethylene glycol dodecyl ether (C12E8) after removal of the proteins from the brush-border membrane vesicles with 2% CHAPS and 4 M urea. When the CHAPS-insoluble protein was treated with papain before its solubilization with C12E8, a substantial amount of protein was removed without any decrease of the transport activities. The solubilized transporters were reconstituted into proteoliposomes after removal of C12E8 with Bio-Beads SM2. Several parameters proved to be important for optimal reconstitution efficiency: (a) the type of detergent, and (b) the phospholipid/protein and detergent/protein ratio during reconstitution, and (c) the salt concentration during reconstitution. Reconstituted proteoliposomes showed rapid uptake of neutral L-alpha-amino acids but not imino acid, basic or acidic amino acids driven by an electrochemical potential of Na+ (out > in). The uptakes under low- and high-substrate condition were further augmented by an artificial membrane potential introduced by K+ diffusion via valinomycin (negative interior). Kinetic analysis revealed that both the brush-border membranes and the solubilized fraction involved two carrier-mediated pathways for alanine transport. The kinetic parameters were determined by curve fitting with a computer to be Kt1 = 0.28 mM (0.21 mM) and Kt2 = 43.2 mM (28.4 mM), respectively (those with brush-border membrane vesicles in parentheses). Studies on the specific activities for transport of individual amino acids under low or high substrate concentration and the cross-inhibitory effects of various amino acids on alanine uptake (low concentration) revealed that these transporters possess broad specificity for neutral L-alpha-amino acids.

Alanine↗

Inhibitory effect of NaN3 on the F0F1 ATPase of submitochondrial particles as related to nucleotide binding.

The inhibitory effects of NaN3 on the F0F1 ATPase of beef heart submitochondrial particles were investigated. It was shown that NaN3 inhibited the ATPase activity only in the presence of ATP or ADP and the inhibition proceeded slowly. Analysis of the time-course of the inhibition process lead to a conclusion that an ATP binding site which has an apparent Kd of 14.0 +/- 8.7 microM is responsible for the increase of NaN3 sensitivity. This value agreed well with the low Km of ATP hydrolysis characterized before (Muneyuki, E., and Hirata, H. (1988) FEBS Lett. 234, 455-458) and in the range of so-called bi-site catalysis. The same conclusion was derived as for isolated F1 ATPase. From similar analysis, the Kd of this site for ADP was deduced to be 1.34 +/- 0.45 microM, which also agreed with that reported by Pedersen (Pedersen, P.L. (1975) Biochem. Biophys. Res. Commun. 64, 610-616) and also in the same range as reported for the low Km of ATP synthesis by activated submitochondrial particles. These results suggest that hydrolysis through the low Km mode of ATPase reaction leads the enzyme NaN3 sensitive form and this reaction cycle corresponds to the low Km mode of ATP synthesis.

Adenosine Diphosphate↗

Tissue-specific isoforms of the bovine mitochondrial ATP synthase gamma-subunit.

Tissue-specific isoforms of the gamma-subunit of the bovine FoF1-ATP synthase were identified for the first time. The two isoforms, heart and liver type, were generated by alternative splicing, the liver-type RNA transcript containing a 37-nucleotide sequence as a cassette exon. Protein sequencing of the C-terminal fragments of the two isoforms of the F1 gamma-subunit indicated that the liver-type isoform had an additional aspartate residue at the C terminus, not present in the heart type one.

Alternative Splicing↗

Effect of chronic ceruletide treatment on dopaminergic neurotransmitters, receptors and their mRNAs in the striatum of rats with dyskinesia induced by iminodipropionitrile.

To clarify the mechanism of long-lasting ceruletide action, an analogue of cholecystokinin, in relieving the dyskinesia induced by the iminodipropionitrile (IDPN), we investigated the changes in dopaminergic neuronal system in the striatum. In the control rats, ceruletide had no significant effect on the concentrations of dopamine (DA), DOPAC or HVA or on the turnover of DA in the striatum. The concentration of DA was decreased and the turnover of DA [(DOPAC + HVA)/DA] was increased in the striatum of IDPN-treated rats. Chronic administration of ceruletide (160 micrograms.kg-1.day-1 x 10 days) increased DA concentration and decreased DA turnover only transiently. Both D1 and D2 receptors and their mRNAs were decreased in the striatum of rats given IDPN. After chronic ceruletide treatment, D1 receptor rose to the control level for 3 days, while the D2 receptor rose to a level 1.5 times the control level for 3 days. Even at the 7 days after chronic ceruletide treatment, D2-R rose significantly as compared with the IDPN-treated rats. Both D1 and D2 receptor mRNAs were significantly increased for 3 days in the IDPN-treated rats. These observations indicate that the synthesis of DA receptors is increased by ceruletide treatment in the striatum of IDPN-treated rats. These changes in DA receptors and their mRNAs closely paralleled the changes in dyskinetic movement of the IDPN-treated rats after repeated daily administration of ceruletide, as previously reported. The parallel changes between the DA receptors and dyskinetic movement suggest that an up-regulation of DA receptors in the striatum corresponds with an improvement of dyskinesia in the IDPN-treated rats.(ABSTRACT TRUNCATED AT 250 WORDS)

3,4-Dihydroxyphenylacetic Acid↗

Ischemia-induced changes in alpha-tubulin and beta-actin mRNA in the gerbil brain and effects of bifemelane hydrochloride.

Using in situ hybridization histochemistry, we examined changes in the cytoskeletal protein alpha-tubulin and beta-actin mRNAs in the gerbil brain 14 days after transient ischemia. In an attempt to identify the changes induced in the synthesis of cytoskeletal protein by ischemia, we also evaluated the effects of post-ischemia administration of bifemelane on these cytoskeletal proteins. alpha-Tubulin and beta-actin mRNAs were decreased in the CA1 region 14 days after transient ischemia. These decreases coincided with the loss of CA1 pyramidal cells, suggesting that they may have been related to delayed neuronal death. The beta-actin mRNA level in ischemic controls was significantly increased in the dentate gyrus, habenular nucleus, and medial and lateral thalamic nuclei, where some afferent nerves project into the hippocampal pyramidal cells. The increased beta-actin mRNA suggests that there may be a compensatory enhancement of actin synthesis in the afferent neurons that restores loosened synaptic connections with the ischemic cells in the CA1-4 fields. Administration of bifemelane just after recirculation prevented most of the ischemia-induced mRNA reductions in the CA1 field. Bifemelane's effect may be related to inhibition of Ca2+ influx and its radical scavenging activity. When bifemelane was administered to the ischemic group, alpha-tubulin mRNA levels significantly increased in the dentate gyrus and amygdaloid nucleus, and beta-actin mRNAs showed a tendency to increase in the CA3 and CA4 fields, dentate gyrus, and medial and lateral thalamic nuclei. These findings suggest that bifemelane may enhance synthesis of cytoskeletal protein, especially in the ischemic brain, inducing axon outgrowth or synapse formation.

Actins↗

Regional changes in neuropeptide levels after 5,7-dihydroxytryptamine-induced serotonin depletion in the rat brain.

The levels of five neuropeptides (substance-P, somatostatin, cholecystokinin octapeptide, methionine-enkephalin and dynorphin) were examined in the brain and the spinal cord of rats 2 weeks after intracerebroventricular injection of 5,7-dihydroxytryptamine (5,7-DHT). 5,7-DHT injection caused a significant reduction of the serotonin level in all regions of the brain. The level of each neuropeptide except dynorphin significantly increased in specific regions of the brain after 5,7-DHT treatment without any decrease in their levels in any region. Since, coexistence and interaction between classical neurotransmitters and neuropeptides in the same neurons have been reported, both are indispensable for evaluating pathophysiological state of the brain function associated with abnormal neural transmission. The present findings together with previous reports suggest that neuropeptides act as neurotransmitters and compensate for the impaired function of the serotonergic systems.

5,7-Dihydroxytryptamine↗

Rapid response of striatal muscarinic M1-receptor mRNA to muscarinic cholinergic agents in rat brain.

The effects of a single administration of muscarinic cholinergic agents on the level of muscarinic M1-receptor messenger RNA (M1-R mRNA) in the rat striatum were studied. Carbachol increased the M1-R mRNA expression rapidly and transiently, while trihexyphenidyl decreased it. These results suggest that muscarinic cholinergic agents participate in the positive regulation of muscarinic receptor mRNA in the early stage after treatment, contrary to the negative regulation in the chronic stage.

Animals↗

[Review of molecular structure and function of ion channels].

Recent research on various ion channel proteins have revealed that they can be classified into several groups of super-families from their structural similarity. Among them, the voltage-gated ion channel super-family, including K(+)-channel, Na(+)-channel and Ca(2+)-channel, consist of four homologous functional units of six transmembrane segments. Site directed mutagenesis applied on those proteins revealed that the 4th segment works as the voltage sensor and the linker (SS1-SS2) between 5th and 6th segments forms the pore structure passing ions. On the other hand, the ligand operated receptor channel super-family, including nicotinic acetylcholine receptor, the GABAA receptor and glutamate receptor, is composed of five subunits which are also homologous. Each subunit contains a large hydrophilic amino-terminal domain which binds ligands and/or competitive blockers, followed by four transmembrane segments. The 2nd segment (MII) of each subunit lines the internal surface of the channel pore as suggested from labelling studies with non-competitive blockers. The ryanodine receptor and the inositol-1,4,5-trisphosphate receptor are also homologous in their structure and are thus classified as a family catalyzing Ca2+ mobilization from intracellular Ca2+ stores. Furthermore, cGMP operated cation channel of vertebrate rod photoreceptor and cAMP operated cation channel of olfactory neuron are composed of almost identical polypeptide, which contains the remnant of the voltage sensor segment. Classification of these channel proteins may provide valuable clues to further understanding the structure/function relationships at molecular levels.

Amino Acid Sequence↗