西岡 孝明

Other和漢医薬学総合研究所年報, 第35巻, 2009.03.31, Page 87-91othe

西岡, 孝明

University of Toyama Repository

scitamrofnI lacidemoiB fo noisiviD 㐷ㇱᨆ⸃ႎᖱ⢻ᯏ  ).D.hP( akoihsiN ikaakaT rosseforP gnitisiV ᣿ቁ ጟ⷏ ᝼ᢎຬቴ㩷㩷 ⊛⋡ⓥ⎇٠ᨆಽቇൻߩ㗇ᔅ߇ᨆಽ㊂⾰ߥᐲᗵ㜞㧘⢻⸃ಽ㜞㧘ߪߢ㊁ಽቇ⑼๮↢ߩߤߥᨆ⸃ࡓ࡯ࡠࡏ࠲ࡔ  㩷ᬌߢ࡞࠻ࠢࡍࠬࠬࡑ㧘ߕࠄࠊ߆߆߽ߦൻ⢻ᕈ㜞ߩᨆಽ㊂⾰ߥ߁ࠃߩߎ㧘ߒ߆ߒޕࠆ޿ߡߞߥߣߩ⾰‛ౝ૕↢ߪࠇߎޕ޿ߥ߉ߔߦ % 3-1 ߪวഀߩ‛วൻࠆࠇߐቯหߜ߁ߩ⾰‛ౝ૕↢ߚࠇߐ಴ޕࠆ޽ߢࠄ߆޿ή߇㧕BDSM㧔ࠬ࡯ࡌ࠲࡯࠺ߚߒ㓸෼ࠍ࡞࠻ࠢࡍࠬࠬࡑBDSM㧘ߒᨆ⸃࡮㓸෼ࠍ࡞࠻ࠢࡍࠬࠬࡑ⢻⸃ಽ㜞ߩ⾰‛ౝ૕↢ࠆࠇ߹฽ߦ⮎කṽ๺㧘ߪߢ㐷ㇱᒰߞࠃߦࠇߎޕࠆߔߣ⊛⋡ࠍߣߎࠆߔༀᡷࠍ₸ቯหߩಽᚑቇൻߩ⮎කṽ๺㧘ߡߞࠃߦߣߎࠆߔൻߦ⢻น߇ߣߎࠆߔᨆ⸃ߦ⚦⹦ࠅࠃࠍଥ㑐ߩߣᕈᵴℂ⮎ߣᚑ⚵ቇൻ㧕߻฽ࠍಽᚑ㊂ᓸ㧔ߩ⮎↢ߡޕࠆࠇߐᓙᦼߣߩ߽ࠆߔਈነߦ᣿⸃ߩ᭴ᯏℂ⮎㧘ࠅߥ㩷㩷 ⷐ᭎ⓥ⎇٠ൻࠬ࡯ࡌ࠲࡯࠺ߣ㓸෼ߩ࡞࠻ࠢࡍࠬࠬࡑ⢻⸃ಽ㜞ߩ⾰‛⻢ઍࠆߔ᦭ࠍᕈᵴℂ⮎㧕Σ࠻ࠢࡍࠬࠬࡑߩ⾰‛⻢ઍᰴੑࠆࠇ߹฽ߦ‛ᬀ㧘ߚࠇߐቯ᷹ߦߢ߹ࠇߎߢᚲⓥ⎇ว✚ቇ⮎කṽ๺ 㩷 SMFOT-TI ⢻⸃ಽ㜞ߢᚲⓥ⎇ᧄ㧘ߚ߹ޕࠆ߼ߔߔࠍൻBDSMߡߞߥߎ߅ࠍൻ࡞࠲ࠫ࠺ߣ㓸෼ߩ࡞ᖱㅧ᭴ቇൻߩࡦࠝࠗ࠻ࠢ࠳ࡠࡊ㧘ߒᨆ⸃ࠍnSM࡞࠻ࠢࡍࠬࠬࡑߩ⮎↢ߚߒቯ᷹ߦߚᣂߡ޿↪ࠍࠬࠬࡑߣㅧ᭴ቇൻޟߥⷐᔅߦቯหߩ࡞࠻ࠢࡍࠬࠬࡑߩಽᚑ⮎↢㧘ߡߞࠃߦߣߎ߁ߥߎ߅ࠍൻႎޕࠆߔⓍ⫾࡮ᨆ⸃ࠍޠଥ㑐ߩߣnSM ࡞࠻ࠢࡍ㩷ൻࠬ࡯ࡌ࠲࡯࠺ߩ࡞࠻ࠢࡍࠬࠬࡑߚߒቯ᷹ߢ5/ ⢻⸃ಽ㜞%. ߩᢱ⹜⮎කṽ๺㧕Τޕࠆߔ㓸෼ࠍ࡞࠻ࠢࡍࠬࠬࡑഀಽ㑆ᤨ಴ṁ㧘ߚߒ಴ᬌ࡮ቯ᷹ߢ5/ ⢻⸃ಽ㜞%. ࠍ‛಴᛽ߩ⮎↢ 㩷ࡍࠬࠬࡑߚߞ߆ߥ߈ߢቯห㧘ߊߥߢߌߛߩ߽ߚ߈ߢቯหࠍ‛วൻ㧘ߪ࡞࠻ࠢࡍࠬࠬࡑߩࠄࠇߎߒߣࠣ࠲ߩ⾰‛⻢ઍࠍ5/㧘ߪ࡞࠻ࠢࡍࠬࠬࡑߚߞ߆ߥ߈ߢቯหࠍ⾰‛⻢ઍޕࠆߔ㓸෼߽࡞࠻ࠢ᛽ࠆߥ⇣㧘ߡ޿ߟߦ⮎↢ߚߒวᷙߩࠄࠇߘ߮ࠃ߅㧘ࠇߙࠇߘ‛ᬀ↪⮎ޕࠆߔൻࠬ࡯ࡌ࠲࡯࠺ߡ⹜ࠍߩ߽ߚߒቯ᷹ߢ 5/ ࡞࠻ࠢࡍࠬࠬࡑࠍᢱ⹜ߚߒᚑ૞ߢᴺ࠼ࡦ࡟ࡉࠆߥ⇣㧘ઙ᧦಴᛽㧘ᴺ಴⾰‛⻢ઍᰴੑߣᨐലℂ⮎ߩᢱ⹜㧘ߡߒ߅ߣࠍセᲧߥ߁ࠃߩߎޕࠆߔߦ߁ࠃࠆ߈ߢセᲧߦߣߏᢱޕࠆߔߦ߆ࠄ᣿ࠍଥ㑐ߩߣᚑ⚵ߩ???????????㩷―78―臨床利用部門㩷٠ේ⪺⺰ᢥ 㩷㩷 1) Abe M, Kubo A, Yamamoto S, Hatoh Y, Murai M, Hattori Y, Makabe H, Nishioka T, & Miyoshi H : Dynamic function of the spacer region of acetogenins in the inhibition of bovine mitochondrial NADH-ubiquinone oxidoreductase (complex I).  Biochemistry, 47(23), 6260-6266, 2008. 㩷 Abstract: Studies of the action mechanism of acetogenins, the most potent and structurally unique inhibitors of bovine heart mitochondrial complex I (NADH-ubiquinone oxidoreductase), are valuable in characterizing the inhibitor binding site in this enzyme. Our previous study deepened our understanding of the dynamic function of the spacer region of bis-THF acetogenins [Abe, M., et al. (2005) Biochemistry 44, 14898-14906] but, at the same time, posed new important questions. First, while the two toxophores (i.e., the hydroxylated THF and the gamma-lactone rings) span a distance shorter than that of the extended 13 carbon atoms [-(CH 2) 13-], what is the apparent optimal length of the spacer for the inhibition of 13 carbon atoms? In other words, what is the functional role of the additional methylene groups? Second, why was the inhibitory potency of the mono-THF derivative, but not the bis-THF derivative, drastically reduced by hardening the spacer covering 10 carbon atoms into a rodlike shape [-CH 2-(C identical withC) 4-CH 2-]? This study was designed not only to answer these questions but also to further disclose the dynamic functions of the spacer. We here synthesized systematically designed acetogenins, including mono- and bis-THF derivatives, and evaluated their inhibitory effects on bovine complex I. With regard to the first question, we demonstrated that the additional methylenes enhance the hydrophobicity of the spacer region, which may be thermodynamically advantageous for bringing the polar gamma-lactone ring into the membrane-embedded segment of complex I. With regard to the second question, we observed that a decrease in the flexibility of the spacer region is more adverse to the action of the mono-THF series than that of the bis-THF series. As a cause of this difference, we suggest that for bis-THF derivatives, one of the two THF rings, being adjacent to the spacer, is capable of working as a pseudospacer to overcome the remarkable decrease in the conformational freedom and/or the length of the spacer. Moreover, using photoresponsive acetogenins that undergo drastic and reversible conformational changes with alternating UV-vis irradiation, we provided further evidence that the spacer region is free from steric congestion arising from the putative binding site probably because there is no receptor wall for the spacer region.㩷 㩷㩷 2) Ishihara A, Hashimoto Y, Tanaka C, Dubouzet JG, Nakao T, Matsuda F, Nishioka T, Miyagawa H, & Wakasa K: The tryptophan pathway is involved in the defense responses of rice against pathogenic infection by serotonin production.  Plant Journal. 54, 481-495, 2008 㩷 Abstract: The upregulation of the tryptophan (Trp) pathway in rice leaves infected by Bipolaris oryzae was indicated by: (i) enhanced enzyme activity of anthranilate synthase (AS), which regulates metabolic flux in the Trp pathway; (ii) elevated levels of the AS (OASA2, OASB1, and OASB2) transcripts; and (iii) increases in the contents of anthranilate, indole, and Trp. The measurement of the contents of Trp-derived metabolites by high-performance liquid chromatography coupled with tandem mass spectrometry revealed that serotonin and its hydroxycinnamic acid amides were accumulated in infected leaves. Serotonin accumulation was preceded by a transient increase in the tryptamine content and by marked activation of Trp decarboxylase, indicating that enhanced Trp production is linked to the formation of serotonin from Trp via tryptamine. Feeding of radiolabeled serotonin to inoculated leaves demonstrated that serotonin is incorporated into the cell walls of lesion tissue. The leaves of a propagating-type lesion mimic mutant (sl, Sekiguchi lesion) lacked both serotonin production and deposition of unextractable brown material at the infection sites, and showed increased susceptibility to B. oryzae infection. Treating the mutant with serotonin restored deposition of brown material at the lesion site. In addition, the serotonin treatment suppressed the growth of fungal hyphae in the leaf tissues of the sl mutant. These findings ―88―indicated that the activation of the Trp pathway is involved in the establishment of effective physical defenses by producing serotonin in rice leaves. 㩷 㩷㩷 3) Sato S, Arita M, Soga T, Nishioka T and Tomita M  : Time-resolved metabolomics reveals metabolic modulation in rice foliage. BMC Systems Biology 2 51doi:10.1186/1752-0509-2-51, 2008. 㩷 Abstract: BACKGROUND: To elucidate the interaction of dynamics among modules that constitute biological systems, comprehensive datasets obtained from "omics" technologies have been used. In recent plant metabolomics approaches, the reconstruction of metabolic correlation networks has been attempted using statistical techniques. However, the results were unsatisfactory and effective data-mining techniques that apply appropriate comprehensive datasets are needed. RESULTS: Using capillary electrophoresis mass spectrometry (CE-MS) and capillary electrophoresis diode-array detection (CE-DAD), we analyzed the dynamic changes in the level of 56 basic metabolites in plant foliage (Oryza sativa L. ssp. japonica) at hourly intervals over a 24-hr period. Unsupervised clustering of comprehensive metabolic profiles using Kohonen's self-organizing map (SOM) allowed classification of the biochemical pathways activated by the light and dark cycle. The carbon and nitrogen (C/N) metabolism in both periods was also visualized as a phenotypic linkage map that connects network modules on the basis of traditional metabolic pathways rather than pairwise correlations among metabolites. The regulatory networks of C/N assimilation/dissimilation at each time point were consistent with previous works on plant metabolism. In response to environmental stress, glutathione and spermidine fluctuated synchronously with their regulatory targets. Adenine nucleosides and nicotinamide coenzymes were regulated by phosphorylation and dephosphorylation. We also demonstrated that SOM analysis was applicable to the estimation of unidentifiable metabolites in metabolome analysis. Hierarchical clustering of a correlation coefficient matrix could help identify the bottleneck enzymes that regulate metabolic networks. CONCLUSION: Our results showed that our SOM analysis with appropriate metabolic time-courses effectively revealed the synchronous dynamics among metabolic modules and elucidated the underlying biochemical functions. The application of discrimination of unidentified metabolites and the identification of bottleneck enzymatic steps even to non-targeted comprehensive analysis promise to facilitate an understanding of large-scale interactions among components in biological systems. 㩷 㩷 㩷㩷 4) Mitsuno H, Sakurai T, Murai M, Yasuda T, Kugimiya S, Ozawa R, Toyohara H, Takabayashi J, Miyoshi H & Nishioka T  : Identification of receptors of main sex-pheromone components of three Lepidopteran species.  European Journal of Neuroscience 28 (5), 893-902, 2008. 㩷 Abstract: Male moths discriminate conspecific female-emitted sex pheromones. Although the chemical components of sex pheromones have been identified in more than 500 moth species, only three components in Bombyx mori and Heliothis virescens have had their receptors identified. Here we report the identification of receptors for the main sex-pheromone components in three moth species, Plutella xylostella, Mythimna separata and Diaphania indica. We cloned putative sex-pheromone receptor genes PxOR1, MsOR1 and DiOR1 from P. xylostella, M. separata and D. indica, respectively. Each of the three genes was exclusively expressed with an Or83b orthologous gene in male olfactory receptor neurons (ORNs) that are surrounded by supporting cells expressing pheromone-binding-protein (PBP) genes. By two-electrode voltage-clamp recording, we tested the ligand specificity of Xenopus oocytes co-expressing PxOR1, MsOR1 or DiOR1 with an OR83b family protein. Among the seven sex-pheromone components of the three moth species, the oocytes dose-dependently responded only to the main sex-pheromone component of the corresponding moth species. In our study, PBPs were not essential for ligand specificity of the receptors. On the phylogenetic tree of insect olfactory receptors, the six sex-pheromone receptors identified in the present and previous studies are grouped in the same subfamily but have no relation with the taxonomy of moths. It is most likely that sex-pheromone receptors have randomly evolved from ―89―ancestral sex-pheromone receptors before the speciation of moths and that their ligand specificity was modified by mutations of local amino acid sequences after speciation. 㩷 㩷 㩷㩷 5) Ichimaru N, Murai M, Kakutani M, Kako NJ, Ishihara A, Nakagawa Y, Nishioka T, Yagi T, & Miyoshi M.  : Synthesis and Characterization of New Piperazine-Type Inhibitors for Mitochondrial NADH-Ubiquinone Oxidoreductase (Complex I). Biochemistry, 47, 10816–10826, 2008. 㩷 Abstract: The mode of action of Deltalac-acetogenins, strong inhibitors of bovine heart mitochondrial complex I, is different from that of traditional inhibitors such as rotenone and piericidin A [Murai, M., et al. (2007) Biochemistry 46 , 6409-6416]. As further exploration of these unique inhibitors might provide new insights into the terminal electron transfer step of complex I, we drastically modified the structure of Deltalac-acetogenins and characterized their inhibitory action. In particular, on the basis of structural similarity between the bis-THF and the piperazine rings, we here synthesized a series of piperazine derivatives. Some of the derivatives exhibited very potent inhibition at nanomolar levels. The hydrophobicity of the side chains and their balance were important structural factors for the inhibition, as is the case for the original Deltalac-acetogenins. However, unlike in the case of the original Deltalac-acetogenins, (i) the presence of two hydroxy groups is not crucial for the activity, (ii) the level of superoxide production induced by the piperazines is relatively high, (iii) the inhibitory potency for the reverse electron transfer is remarkably weaker than that for the forward event, and (iv) the piperazines efficiently suppressed the specific binding of a photoaffinity probe of natural-type acetogenins ([ (125)I]TDA) to the ND1 subunit. We therefore conclude that the action mechanism of the piperazine series differs from that of the original Deltalac-acetogenins. The photoaffinity labeling study using a newly synthesized photoreactive piperazine ([ (125)I]AFP) revealed that this compound binds to the 49 kDa subunit and an unidentified subunit, not ND1, with a frequency of approximately 1:3. A variety of traditional complex I inhibitors as well as Deltalac-acetogenins suppressed the specific binding of [ (125)I]AFP to the subunits. The apparent competitive behavior of inhibitors that seem to bind to different sites may be due to structural changes at the binding site, rather than occupying the same site. The meaning of the occurrence of diverse inhibitors exhibiting different mechanisms of action is discussed in light of the functionality of the membrane arm of complex I. 㩷 㩷 㩷㩷 6) Horai, H. and Nishioka, T.: Automatic Generation of Structure of Phospholipids. Journal of Computer Aided Chemistry, 9, 55-61, 2008. 㩷 Abstract: An algorithm and a tool for automatic generation of structures of phospholipids are proposed. The input is a compact representation of the variable part of phospholipids in a systematic way. The output is a structure of the phospholipid represented in the MDL Molfile format. The output molfile describes not only the topological connectivity of atoms but also the 2D coordinate of each atom in order to draw the structure without any overlapping.  The variation of phospholipids that the tool covers includes glycerophospholipids (phosphatidylcholines, phosphatidylethanolamines, phosphatidylglicerols, phosphatidylinositols and phosphatidylserines) and sphingophospholipids with arbitrary length and arbitrary number of double bonds at arbitrary positions and in arbitrary cis/trans isomerism. 㩷 㩷 㩷٠✚ ⺑㩷 㩷㩷 1) ⬑⩫ዏᐘ㧘⷏ጟቁ᣿㧘̌ ࡔ࠲ࡏࡠ࡯ࡓ⸃ᨆߩߚ߼ߩ⾰㊂ಽᨆࠬࡍࠢ࠻࡞࡮࠺࡯࠲ࡌ࡯ࠬ㧦MassBank̍ታ㛎කቇ㧘26(7), 1155-1160, 2008. 㩷 2㧕 ⷏ጟቁ᣿㧘̌ ᓸ↢‛ߩࡔ࠲ࡏࡠ࡯ࡓ⸃ᨆ 㧘̍ޟ21਎♿ߩㄘቇޠ╙㧢Ꮞ㧔ᬀ↰ల⟤✬㓸㧕㧘੩ㇺᄢቇ಴ ળ㧘207-248, 2008. 㩷 㪊㪀㩷 ⷏ጟቁ᣿㧘̌ ⾰㊂ಽᨆᴺᬌ಴↪ૐಽሶ࠺࡯࠲ࡌ࡯ࠬߩ᭴▽ 㧘̍ޟ⑼ቇᛛⴚ࡮⎇ⓥ㐿⊒ߩ࿖―90―㓙Ყセޠ ᐕ 㧘,56 ⎇ⓥ㐿⊒ᚢ⇛࠮ࡦ࠲࡯߇వ┵⸘᷹ᛛⴚಽ㊁✬㓸㧘⊒ⴕޕ㩷 㩷 ٠ቇળႎ๔ 㧔․೎⻠Ṷ㧘ࠪࡦࡐࠫ࠙ࡓ㧘ࡢ࡯࡚ࠢࠪ࠶ࡊ╬㧕㩷 1) ⬑⩫ዏᐘ㧘⷏ጟቁ᣿㧘᦭↰ᱜⷙ㧦̌ ᖱႎ⑼ቇ߆ࠄ⷗ߚࠬࡍࠢ࠻࡞࠺࡯࠲ࡌ࡯ࠬMassBank 㧘̍ࠪࡦࡐࠫ࠙ࡓޟ࠺࡯࠲ࡌ࡯ࠬ߆ࠄ߽߭ߣߊ⾰㊂ಽᨆᖱႎቇޠ㧘╙ 56 ࿁⾰㊂ಽᨆ✚ว⸛⺰ળ㧔ᣣᧄ⾰㊂ಽᨆቇળਥ௅㧕㧘ߟߊ߫࿖㓙ળ⼏႐㧘ߟߊ߫Ꮢ㧘2008ᐕ 5᦬ 14-16ᣣ㩷 2) Horai, H., Arita, M. and Nishioka, T. Comparison of ESI-MS in MassBank Database. 1st International Conference on BioMedical Engineering and Informatics, Sanya, Hainan, China, 2008ᐕ 5᦬ 28ᣣ㨪30ᣣ.㧔ᩏ⺒޽ࠅ㧕㩷 3) Horai H, Arita M, & Nishioka T, ̌ MassBank: Mass Spectral Database for Metabolome Analysis ,̍56th ASMS Conference on Mass Spectrometry, (American Association for Mass Spectrometry ਥ௅), Colorado Convention Center, Denver, Colorado, USA, 2008ᐕ 6᦬ 1ᣣ㨪5ᣣ.㩷 4) Horai H, Nishioka T. & Arita M, ̌ MassBank: Mass Spectral Database for Metabolome Analysis ,̍5th International Conference on Plant Metabolomics 㧔ญ㗡⊒⴫㧕, Pacifico Yokohama, Yokohama, Japan, 2008ᐕ 7᦬ 15ᣣ㨪18ᣣ.㧔ᩏ⺒޽ࠅ㧕㩷 5) Sakurai T, Mitsuno H, Uchino K, Sezutsu H, Tamura T, Yokohari F, Nishioka T, and Kanzaki R., ̌Activation of bombykol receptor neurons by ectopically expressed olfactory receptor triggers pheromone searching behavior in male silkmoths̍, International Symposium on Olfaction and Taste (ISOT2008), San Francisco, USA, 2008ᐕ 7᦬ 21ᣣ㨪26ᣣ.㩷 6) Horai, H., Arita, M. and Nishioka, T. MassBank: A Mass Spectral Database for Metabolomics. 4th Annual Conference for Metabolomincs㧘Boston, USA, 2008ᐕ 9᦬ 12ᣣ㨪16ᣣ.㩷 7) ⬑⩫ዏᐘ㧘⷏ጟቁ᣿㧘᦭↰ᱜⷙ㧘̌ MassBank:ࡔ࠲ࡏࡠ࡯ࡓ⸃ᨆߩߚ߼ߩ⾰㊂ಽᨆࠬࡍࠢ࠻࡞࠺࡯࠲ࡌ࡯ࠬ 㧘̍╙ 33࿁ᣣᧄක↪ࡑࠬࠬࡍࠢ࠻࡞ቇળ㧘᧲੩ᄢቇ㧘᧲੩ㇺ㧘2008ᐕ9᦬ 25ᣣ㨪26ᣣ.㩷 8) ⷏ጟቁ᣿㧘̌MassBank: Private library ߆ࠄ᭴ㅧផቯ߹ߢ 㧘̍╙ 68࿁ർ㒽⾰㊂ಽᨆ⺣⹤ળ㧔ᣣᧄක↪ࡑࠬࠬࡍࠢ࠻࡞ቇળർ㒽ᡰㇱળ㧕㧘㧔᜗ᓙ⻠Ṷ㧕㧘ንጊᄢቇ㧘ንጊᏒ㧘2008ᐕ 11᦬29ᣣ.㩷―91―

機能情報部門(臨床利用部門,各部門・附属センターの活動と業績)

Other和漢医薬学総合研究所年報, 第36巻, 2010.03.31, Page 97-100othe

―97―臨床利用部門―98――99――100―

https://toyama.repo.nii.ac.jp/?action=repository_action_common_download&item_id=16140&item_no=1&attribute_id=18&file_no=1

機能情報部門(臨床利用部門,各部門・附属センターの活動と業績)

Abstract

Similar works

Full text

Available Versions

University of Toyama Repository

University of Toyama Repository