Yasuo Kakimoto’s research while affiliated with Ehime University and other places

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Publications (123)


Distribution of ?-(?-Aminobutyryl)-Hypusine
  • Article

October 2006

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14 Reads

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1 Citation

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Yasuo Kakimoto

The distribution of -(-aminobutyryl)-hypusine was examined in several organs of the rabbit and in the brain of the rat, rabbit, dog, ox, and monkey. The peptide occurred only in the brains, but appeared to be absent from dog brain. Concentrations were higher in the cerebral hemispheres than in other portions of the brain. No significant difference between white and gray matter was observed.


Isolation and Identification of Methylarginines from Bovine Brain

October 2006

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13 Reads

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9 Citations

Methylarginines in free form were identified in bovine brain. Three compounds were isolated from the basic aliphatic amino acid fraction of bovine brain with several ion-exchange chromatographies. They showed the same Rf values in paper and thin-layer chromatographies as those of authentic NG-monomethylarginine, NG-dimethylargi-nine, and NG-dimethylarginine. The migration distance of the isolated compounds in high-voltage paper electropho-resis and the retention times in ion-exchange HPLC were also identical to those of the above authentic methylarginines. We concluded that these three compounds are the methyl derivatives of arginine described above. The amount of these three compounds isolated from 1,090 g of bovine brain was 0.3 μmol of NG-monomethylarginine, 0.1 μmol of NG,NG-dimethylarginine, and 0.5 μmol of NG,NG-dimethylarginine. The occurrence of these free methylarginines may have an important role in regulating the signal transduction through the nitric oxide system.


Isolation and Identification of ?-(?-Aminobutyryl)-Hypusine

October 2006

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15 Reads

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4 Citations

A new dipeptide, α-(-γ-aminobutyryl)-hypusine, was identified in bovine brain. This compound was isolated from trichloroacetic acid-soluble fraction of bovine brain with five steps of ion-exchange chromatography. Its structure was postulated by routine chemical analyses and determined by synthesis. The amount of the compound isolated from 1.2 kg of bovine brain was 870 nmol.




The 3′-Untranslated Region of Mouse Myelin Basic Protein Gene Increases the Amount of mRNA in Immortalized Mouse Oligodendrocytes

December 1994

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4 Reads

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14 Citations

Biochemical and Biophysical Research Communications

The 3'-untranslated region (UTR) of the myelin basic protein (MBP) mRNA has been found previously to enhance the translational efficiency of the coding region by two-fold in cell-free translational systems. In this study, we transfected eukaryotic expression vectors containing the reporter cDNA for chloramphenicol acetyltransferase (CAT) with or without the mouse MBP cDNA 3'-UTR into cultured cells. CAT activity in the mouse oligodendrocyte cell line, N20.1, transfected with a CAT cDNA containing the MBP 3'-UTR [CAT-MBP 3'-UTR], was twice as high as that of the CAT cDNA without the 3'-UTR; CAT activities for the two constructs were the same in the mouse fibroblast cell line, NIH 3T3. Using reverse transcriptase PCR quantitative analysis, the expression of mRNA was determined. The level of the [CAT-MBP 3'-UTR] mRNA was about ten times higher than CAT mRNA in N20.1 cells but they were the same in NIH 3T3 cells. We conclude that the 3'-UTR of MBP gene increases gene expression at both the mRNA and protein levels in oligodrocyte cell lines, probably through a post-transcriptional mechanism such a message stabilization.


Protection by Prosaposin Against Ischemia-Induced Learning Disability and Neuronal Loss

November 1994

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12 Reads

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105 Citations

Biochemical and Biophysical Research Communications

Prosaposin, the protein precursor of saposins A, B, C, and D which activate sphingolipid hydrolases, is abundant in several brain regions including the hippocampus. We infused prosaposin continuously for 7 days into the lateral ventricle of gerbils starting 3 hours before 3-min of forebrain ischemia. Using the step-down passive avoidance task, we demonstrated that ischemia-induced learning disability is prevented almost completely by prosaposin infusion. Subsequent light and electron microscopic examinations showed that pyramidal neurons in the CA1 field of the hippocampus as well as synapses within the strata moleculare, lacunosum/radiatum and oriens of the field were significantly more numerous in gerbils infused with prosaposin infusion than in those receiving saline infusion. These findings suggest that prosaposin possesses neurotrotrophic activity to protect hippocampal CA1 neurons from lethal ischemic damage.


Day‐Night Variation of Urine Volume in Parkinson's Disease

October 1994

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28 Reads

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11 Citations

The Japanese journal of psychiatry and neurology

Studies on the circadian rhythm of urine excretion in healthy men have demonstrated that the maximal urine flow occurs in the early afternoon and the minimal around midnight. In this study, an abnormality in the variation of urine volume was found in parkinsonian patients. Urine samples were collected during daytime (9:00-21:00) and nighttime (21:00-9:00). Fifteen healthy control subjects were examined and found to excrete 60% during the daytime and 40% during the nighttime of the total urine volume. Sixteen parkinsonian patients excreted 43% during the daytime and 57% during the nighttime. In contrast to the control subjects, the parkinsonian patients excreted a smaller volume of their urine during the daytime than during the nighttime. This finding might be related to the degeneration of dopaminergic and/or nondopaminergic neurons in the brain which control urinary excretion.


Anticipation in hereditary dentatorbral-pallidoluysian atrophy

July 1994

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9 Reads

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33 Citations

Human Genetics

Anticipation refers to the progressively earlier onset and increase in disease severity in successive generations. We studied four families with hereditary dentatorubral-pallidoluysian atrophy (DRPLA), a neurodegenerative disease, and anticipation was present in the mode of inheritance. In subsequent generations DRPLA shows an earlier onset and more severe as well as additional symptoms. Older onset patients suffer from cerebellar ataxia with or without dementia, whereas younger onset patients present as progressive myoclonus epilepsy syndrome, which consists of mental retardation, dementia, and cerebellar ataxia as well as epilepsy and myoclonus. Anticipation with paternal transmission was significantly greater than with maternal transmission.



Citations (74)


... The history of dimethylarginines in medicine began in 1970, when they were first isolated from human urine [1]. At present, asymmetric dimethylarginine (ADMA) and symmetric dimethylarginine (SDMA) are recognised uraemic toxins [2]. ...

Reference:

Asymmetric and Symmetric Dimethylarginines as Renal Function Parameters in Paediatric Kidney Diseases: A Literature Review from 2003 to 2022
Isolation and Identification of Ng, Ng-and Ng, N'g-Dimethylarginine, Nε-Mono-, Di-, and Trimethyllysine, and Glucosylgalactosyl-and Galactosyl-δ-hydroxylysine from Human Urine
  • Citing Article
  • Full-text available
  • November 1970

Journal of Biological Chemistry

... A well known example of enzyme-lacking specificity is the ligase that catalyzes the synthesis of carnosine (␤-alanyl-histidine; ␤-Ala-His) in skeletal muscle and homocarnosine (␥-aminobutyryl-histidine; GABA-His) in brain (11)(12)(13)(14)(15). Carnosine is an abundant dipeptide present in the skeletal muscle of many vertebrates where it serves as a pH buffer (for review, see Ref. 16) and maybe also as a radical scavenger (17). ...

α-(γ-Aminobutyryl)-lysine in mammalian brain: Its identification and distribution
  • Citing Article
  • March 1969

... Measurement of the activity of BAIBPAT in patients with hyper-β-aminoisobutyric aciduria is not indicated, because this condition is thought to be a benign polymorphism. It has been reported that genetic high excretors have less than 10% normal transaminase activity in liver (Taniguchi et al 1972). ...

Deficiency of d-β-aminoisobutyrate: Pyruvate aminotransferase in the liver of genetic high excretors of d-β-aminosobutyrate
  • Citing Article
  • October 1972

Biochimica et Biophysica Acta (BBA) - General Subjects

... Therefore, the liver might be a promising target for further research with respect to the endogenous source of BAIBA's enantiomers by exercise. Additionally, dipeptides containing BAIBA have been measured in mammalian tissue (Morris et al., 1961;Kakimoto et al., 1965) which could also be relevant to look at, especially since the metabolically linked β-alanine is mainly stored in muscle in conjugation with histidine (β-alanyl-L-histidine, also called carnosine) (Boldyrev et al., 2013). ...

Isolation of γ-l-glutamyl-l-β-aminoisobutyric acid from bovine brain
  • Citing Article
  • May 1965

Biochimica et Biophysica Acta (BBA) - General Subjects

... However, the correlation between FGR and 2-AEP has not yet been elucidated. Rats and other higher vertebrates cannot generate 2-AEP, which contains a carbon-phosphorus bond [62,63]. Ruminant protozoa can synthesize protein-bound and lipid-bound forms of 2-AEP as well as the free form of 2-AEP [64]. ...

Isolation and Identification of 2-Aminoethyl-phosphonic Acid from Bovine Brain
  • Citing Article
  • September 1965

... The translation factor elF5A is essential for early embryonic development [137] and for the activation of the autophagy pathway, and the hypusine modification is crucial for its proper activity [44,138]. Putreanine ( Figure 3) is yet another product of PA catabolism [122,139,140]. Initially, putreanine was thought to be a unique metabolite of mammalian central nervous PA catabolism [139] but was later also detected in rat liver and kidney [122]. ...

Putreanine, N-(4-Aminobutyl)-3-aminopropionic Acid

Journal of Biological Chemistry

... Free hypusine is derived from the degradation of eIF5A, since no pathway for free hypusine synthesis has been found. Dipeptides containing hypusine, α(γ-aminobutyryl )-hypusine (or GABA-hypusine) (Sano et al., 1986; Sano et al., 1987) and α-(β-alanyl)hypusine (Ueno et al., 1991 ), were isolated from mammalian brain, but the biosynthesis pathway and function of these hypusine-containing peptides remain unclear. eIF5A was originally isolated from ribosomes of rabbit reticulocytes as one of the proteic components that are required for synthesis of methionyl-puromycin, an assay used to investigate factors involved in initiation of translation (Kemper et al., 1976). ...

Distribution of ?-(?-Aminobutyryl)-Hypusine
  • Citing Article
  • October 2006

... Besides hypusine in the free form, dipeptides containing hypusine were also identified in mammalian brains, such as α-(γ-aminobutyryl)-hypusine (GABA-hypusine) (Sano et al. 1986) and α-(β-alanyl)-hypusine (Ueno et al. 1991). The mammals naturally produce several other dipeptides with similar structures to hypusine-containing dipeptides, such as α-(β-alanyl)-l-histidine (carnosine) and α-(γ-aminobutyryl)l-histidine (homocarnosine) (Kwiatkowski et al. 2018). ...

Isolation and Identification of ?-(?-Aminobutyryl)-Hypusine
  • Citing Article
  • October 2006

... This reaction is considered particularly important because it diminishes NO bioavailability. Besides ADMA, there are additional endogenous and exogenous N G -substituted L-arginine inhibitors of NOS activity (1,(6)(7)(8)(9)(10)(11)(12)(13)(14)(15)(16)(17)(18)(19). Yet, only ADMA has been suggested as a potent risk factor for the development of NOassociated endothelial dysfunction and cardiovascular diseases in humans due to its inhibitory action on eNOS (20,21). ...

Isolation and Identification of Methylarginines from Bovine Brain
  • Citing Article
  • October 2006