9 results on '"Kanaki N"'
Search Results
2. Development of a canine blood C-reactive protein-measuring device using a flow-type immunosensor.
- Author
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Kubota T, Tateishi N, Toita H, Kanaki N, Hata A, and Fujitani N
- Subjects
- Animals, Dogs, Immunoassay methods, Immunosorbents, Reproducibility of Results, Biosensing Techniques, C-Reactive Protein analysis
- Abstract
This study aimed to construct a measurement system with the same performance as a measurement system using an automated analyzer and immunoturbidimetric reagents (comparative method) using a flow-type immunosensor (FIS) based on the fluorescence-linked immunosorbent assay technology. In the FIS constructed in this study, all control samples were within the indicated values. The coefficient of variation of repeatability and intermediate precision were less than 2.4% and less than 4.4%, respectively. The lower limit of quantification in this measurement system was 3.9 mg/L, and linearity was confirmed for quantification values, ranging from 3.9 to 465 mg/L. Canine plasma samples (N = 39) were used to measure C-reactive protein (CRP) levels using the comparative method (x) and FIS (y). The regression equation between the measurements was y = 1.035 × - 0.002, with a correlation coefficient of 0.9809, indicating a significantly high correlation. Although the Brandt-Altman analysis suggested the possibility of a proportional systematic error between the two measurements, 38 of the 39 canine plasma samples measured fell within the acceptable range of error, indicating that the measurements are highly consistent. These results suggest that the analytical accuracy of the FIS constructed in this study and the quantitative value of canine CRP are equivalent to those of measurement systems using automated analyzers and immunoturbidimetric reagents., (© 2022. The Author(s), under exclusive licence to The Japan Society for Analytical Chemistry.)
- Published
- 2022
- Full Text
- View/download PDF
3. Acacia arabica ( Lam. ) Willd. On osteoblastogenesis, osteoblast proliferation, osteoclastic activity, and bone calcium mineralization.
- Author
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Kakadia N, Vegad K, and Kanaki N
- Subjects
- Alkaline Phosphatase, Animals, Anthraquinones, Calcium, Cell Proliferation, Osteoblasts physiology, Plant Extracts pharmacology, Rats, Acacia, Osteoclasts
- Abstract
Objectives: Since ancient times Acacia arabica ( Lam. ) Willd. (AA) consumed for the bone and muscle related disorder like the bone fracture, rheumatoid arthritis, and bone loss. To study the effects of the aqueous (AAA) and ethanolic extract (AAE) of AA on osteoblast proliferation and differentiation, osteoclastic activity and bone matrix mineralization using in vitro primary bone-marrow cultures., Methods: Effect of AAA and AAE was estimated using four in vitro assays. Primary bone marrow cell culture, isolated from rat femur bone, was used for all the assays. Cell growth and viability were assessed by standard colorimetric assays like MTT assay. The differentiation of mesenchymal stem cells into osteoblastic lineage was evaluated by the measuring the levels of the osteoblast-specific marker, alkaline phosphatase. Antiosteoclastic action and matrix mineralization were measured using TRAP assay and Alizarin red-s staining assay, respectively., Results: It indicates that AAA causes more increase in osteoblast differentiation and a reduction in osteoclast activity as compared to AAE. In osteoblast proliferation assay, AAA was found to promote more cell proliferation as compared to AAE. Higher concentrations of AAA significantly increased mineralization of bone-like matrix., Conclusions: The extracts of AA have a significant positive influence on osteogenesis and they inhibit osteoclastogenesis. Hence, these extracts have the potential to be developed as a therapy for osteoporosis., (© 2022 Walter de Gruyter GmbH, Berlin/Boston.)
- Published
- 2022
- Full Text
- View/download PDF
4. Anti-osteoporotic effect of Terminalia arjuna (Roxb.) Wight & Arn . in bilateral ovariectomized induced post-menopausal osteoporosis in experimental rats.
- Author
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Kakadia N and Kanaki N
- Abstract
Objectives: In ancient times Terminalia arjuna (Roxb.) Wight & Arn. (TA) was used for fast healing of fracture and to strengthen the bone. However, no scientific study has been done to validate its usefulness in the alleviation of osteoporosis. To investigate the efficacy of stem bark TA against post-menopausal osteoporosis using bilateral ovariectomized rat model., Methods: Aqueous (TAA) and methanolic (TAM) extracts of TA was evaluated for its anti-osteoporotic activity. Sham control rats were allotted as Group I (Normal control); Group II animals acted as OVX control (Disease control); Group III OVX rats were treated with estrogen (Standard group - 2 mg/kg) Group IV and V OVX rats give treatment to TAA (250 and 500 mg/kg, p.o.), respectively. This treatment is continue for the four weeks and at the end, serum biochemical parameters such as serum calcium and alkaline phosphate were evaluated. Femoral bone parameters (Compression of vertebrae, femoral neck load testing, Three point bending of tibia, Femur length and weight), histology, body weight, and fifth lumbar vertebra breaking strength were also assessed after the sacrificing the animal., Results: In OVX rats, atrophy of uterus and descent of BMD were suppressed by treatment with TAA and TAM. In addition, TAM 500 completely corrected the decreased serum concentration of Calcium, Phosphorus, ALP and TRAP observed in OVX rats. TAA and TAM both increased biomechanical strength significantly in comparison to the sham group. Histological results also revealed its protective action through elevation of bone formation. TAM significantly increase the uterine and femoral bone weight The TAM showed maximum anti-osteoporotic activity in in vivo study as compare to TAA., Conclusions: The results, evaluated on the basis of biochemical, bone mineral density, biomechanical, and histopathological parameters, presented that TAA and TAM has a definite antiosteoporotic effect, like to estrogen, especially effective for inhibition bone fracture induced by estrogen deficiency., (© 2021 Walter de Gruyter GmbH, Berlin/Boston.)
- Published
- 2021
- Full Text
- View/download PDF
5. UDP-N-acetylglucosamine-dolichyl-phosphate N-acetylglucosaminephosphotransferase is indispensable for oogenesis, oocyte-to-embryo transition, and larval development of the nematode Caenorhabditis elegans.
- Author
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Kanaki N, Matsuda A, Dejima K, Murata D, Nomura KH, Ohkura T, Gengyo-Ando K, Yoshina S, Mitani S, and Nomura K
- Subjects
- Animals, Caenorhabditis elegans metabolism, Embryo, Nonmammalian metabolism, Oocytes metabolism, Oogenesis genetics, Transferases (Other Substituted Phosphate Groups) metabolism
- Abstract
N-linked glycosylation of proteins is the most common post-translational modification of proteins. The enzyme UDP-N-acetylglucosamine-dolichyl-phosphate N-acetylglucosaminephosphotransferase (DPAGT1) catalyses the first step of N-glycosylation, and DPAGT1 knockout is embryonic lethal in mice. In this study, we identified the sole orthologue (algn-7) of the human DPAGT1 in the nematode C. elegans. The gene activity was disrupted by RNAi and deletion mutagenesis, which resulted in larval lethality, defects in oogenesis and oocyte-to-embryo transition. Endomitotic oocytes, abnormal fusion of pronuclei, abnormal AB cell rotation, disruption of permeation barriers of eggs, and abnormal expression of chitin and chitin synthase in oocytes and eggs were the typical phenotypes observed. The results indicate that N-glycosylation is indispensable for these processes. We further screened an N-glycosylated protein database of C. elegans, and identified 456 germline-expressed genes coding N-glycosylated proteins. By examining RNAi phenotypes, we identified five germline-expressed genes showing similar phenotypes to the algn-7 (RNAi) animals. They were ribo-1, stt-3, ptc-1, ptc-2, and vha-19. We identified known congenital disorders of glycosylation (CDG) genes (ribo-1 and stt-3) and a recently found CDG gene (vha-19). The results show that phenotype analyses using the nematode could be a powerful tool to detect new CDG candidate genes and their associated gene networks.
- Published
- 2019
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6. Chondroitin 4-O-Sulfotransferase Is Indispensable for Sulfation of Chondroitin and Plays an Important Role in Maintaining Normal Life Span and Oxidative Stress Responses in Nematodes.
- Author
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Izumikawa T, Dejima K, Watamoto Y, Nomura KH, Kanaki N, Rikitake M, Tou M, Murata D, Yanagita E, Kano A, Mitani S, Nomura K, and Kitagawa H
- Subjects
- Animals, Caenorhabditis elegans genetics, Caenorhabditis elegans Proteins genetics, Cell Division, Female, Heparitin Sulfate metabolism, Male, Sequence Deletion, Sulfates metabolism, Sulfotransferases genetics, Caenorhabditis elegans enzymology, Caenorhabditis elegans growth & development, Caenorhabditis elegans Proteins metabolism, Chondroitin metabolism, Chondroitin Sulfates metabolism, Oxidative Stress, Sulfotransferases metabolism
- Abstract
Chondroitin sulfate (CS)/chondroitin (Chn) chains are indispensable for embryonic cell division and cytokinesis in the early developmental stages in Caenorhabditis elegans and mice, whereas heparan sulfate (HS) is essential for axon guidance during nervous system development. These data indicate that the fundamental functions of CS and HS are conserved from worms to mammals and that the function of CS/Chn differs from that of HS. Although previous studies have shown that C. elegans produces HS and non-sulfated Chn, whether the organism produces CS remains unclear. Here, we demonstrate that C. elegans produces a small amount of 4-O-sulfated Chn and report the identification of C41C4.1, an orthologue of the human chondroitin 4-O-sulfotransferase gene. Loss of C41C4.1 in C. elegans resulted in a decline in 4-O-sulfation of CS and an increase in the number of sulfated units in HS. C41C4.1 deletion mutants exhibited reduced survival rates after synchronization with sodium hypochlorite. Collectively, these results show for the first time that CS glycans are present in C. elegans and that the Chn 4-O-sulfotransferase responsible for the sulfation plays an important role in protecting nematodes from oxidative stress., (© 2016 by The American Society for Biochemistry and Molecular Biology, Inc.)
- Published
- 2016
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7. RNAi screening of human glycogene orthologs in the nematode Caenorhabditis elegans and the construction of the C. elegans glycogene database.
- Author
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Akiyoshi S, Nomura KH, Dejima K, Murata D, Matsuda A, Kanaki N, Takaki T, Mihara H, Nagaishi T, Furukawa S, Ando KG, Yoshina S, Mitani S, Togayachi A, Suzuki Y, Shikanai T, Narimatsu H, and Nomura K
- Subjects
- Animals, Base Sequence, Caenorhabditis elegans growth & development, Caenorhabditis elegans metabolism, Caenorhabditis elegans Proteins antagonists & inhibitors, Caenorhabditis elegans Proteins chemistry, Caenorhabditis elegans Proteins metabolism, Carbohydrate Sequence, Cell Cycle Proteins antagonists & inhibitors, Cell Cycle Proteins chemistry, Cell Cycle Proteins metabolism, Endoplasmic Reticulum Stress genetics, Gene Expression Regulation, Developmental, Genotype, Germ Cells cytology, Germ Cells metabolism, Glycoconjugates chemistry, Glycoconjugates metabolism, Glycosaminoglycans chemistry, Glycosaminoglycans metabolism, Glycosphingolipids chemistry, Glycosphingolipids metabolism, Humans, Meiosis genetics, Mitosis genetics, Molecular Sequence Data, Phenotype, RNA, Small Interfering genetics, RNA, Small Interfering metabolism, Sequence Homology, Nucleic Acid, Caenorhabditis elegans genetics, Caenorhabditis elegans Proteins genetics, Cell Cycle Proteins genetics, Databases, Genetic, Genes, Helminth, RNA Interference
- Abstract
In this study, we selected 181 nematode glycogenes that are orthologous to human glycogenes and examined their RNAi phenotypes. The results are deposited in the Caenorhabditis elegans Glycogene Database (CGGDB) at AIST, Tsukuba, Japan. The most prominent RNAi phenotypes observed are disruptions of cell cycle progression in germline mitosis/meiosis and in early embryonic cell mitosis. Along with the previously reported roles of chondroitin proteoglycans, glycosphingolipids and GPI-anchored proteins in cell cycle progression, we show for the first time that the inhibition of the functions of N-glycan synthesis genes (cytoplasmic alg genes) resulted in abnormal germline formation, ER stress and small body size phenotypes. The results provide additional information on the roles of glycoconjugates in the cell cycle progression mechanisms of germline and embryonic cells., (© The Author 2014. Published by Oxford University Press. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.)
- Published
- 2015
- Full Text
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8. Synergistic potentiation of anti-anxiety activity of valerian and alprazolam by liquorice.
- Author
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Bhatt C, Kanaki N, Nayak R, and Shah G
- Subjects
- Animals, Drug Synergism, Male, Mice, Phytotherapy, Alprazolam pharmacology, Anti-Anxiety Agents pharmacology, Anxiety drug therapy, Glycyrrhiza, Plant Extracts pharmacology, Valerian chemistry
- Published
- 2013
- Full Text
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9. A rapid method for isolation of piperine from the fruits of Piper nigrum Linn.
- Author
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Kanaki N, Dave M, Padh H, and Rajani M
- Subjects
- Calorimetry, Differential Scanning, Chromatography, Thin Layer, Fruit, Reference Standards, Spectrum Analysis, Transition Temperature, Alkaloids isolation & purification, Benzodioxoles isolation & purification, Piper nigrum chemistry, Piperidines isolation & purification, Plant Extracts chemistry, Polyunsaturated Alkamides isolation & purification
- Abstract
A simple, rapid and efficient method has been developed for the isolation of piperine from the fruits of Piper nigrum. The method involves extraction of the fruit powder with glacial acetic acid, from which piperine is partitioned into chloroform and subsequently crystallized. The identity of the compound was confirmed by its melting point, comparison of UV, IR, and mass spectral data with those from a reference standard, and co-chromatography with the reference standard using thin-layer chromatography (TLC). The purity of the compound was ascertained by TLC, by recording UV absorption spectra at the start, middle, and end positions of the spot on the plate, and by differential scanning calorimetry (DSC).
- Published
- 2008
- Full Text
- View/download PDF
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