Metabolomic profiling of the autosomal dominant polycystic kidney disease rat model

Takafumi Toyohara, Takehiro Suzuki, Yasutoshi Akiyama, Daisuke Yoshihara, Yoichi Takeuchi, Eikan Mishima, Koichi Kikuchi, Chitose Suzuki, Masayuki Tanemoto, Sadayoshi Ito, Shizuko Nagao, Tomoyoshi Soga, Takaaki Abe

研究成果: Article

20 引用 (Scopus)

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Background: Autosomal dominant polycystic kidney disease (ADPKD) is an inherited systemic disease characterized by renal cyst expansion, resulting in renal failure. With the progression of renal damage, the accumulation of uremic compounds is recently reported to subsequently cause further renal damage and hypertension. Finding uremic toxins and sensitive markers for detecting the early stage of ADPKD is necessary to clarify its pathophysiological process and to prevent its progression. The aim of this study was to analyze the profile of uremic retention solutes of ADPKD by capillary electrophoresis-mass spectrometry (CE-MS) using the Han:SPRD rat model. Methods: Two hundred and ninety-seven cations and 190 anions were comprehensively analyzed by CE-MS in Han:SPRD rats and control rats. Results: We found 21 cations and 19 anions that accumulated significantly in the heterozygous (Cy/+) ADPKD rat model compared with control rats. Among the compounds, increases in 5-methyl-2′-deoxycytidine, glucosamine, ectoine, allantoate, α-hydroxybenzoate, phenaceturate and 3-phenylpropionate and decreases in 2-deoxycytidine, decanoate and 10-hydroxydecanoate were newly identified in the ADPKD Cy/+ rats. Conclusion: We identified uremic retention solutes in ADPKD Cy/+ rats. Compounds related to ADPKD could be useful markers for detecting the early stage of ADPKD.

元の言語English
ページ(範囲)676-687
ページ数12
ジャーナルClinical and Experimental Nephrology
15
発行部数5
DOI
出版物ステータスPublished - 01-10-2011

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Autosomal Dominant Polycystic Kidney
Metabolomics
5-methyldeoxycytidine
Capillary Electrophoresis
Anions
Cations
Mass Spectrometry
Decanoates
Kidney
Hydroxybenzoates
Deoxycytidine
Renal Hypertension
Glucosamine
Renal Insufficiency
Cysts

All Science Journal Classification (ASJC) codes

  • Physiology
  • Nephrology
  • Physiology (medical)

これを引用

Toyohara, T., Suzuki, T., Akiyama, Y., Yoshihara, D., Takeuchi, Y., Mishima, E., ... Abe, T. (2011). Metabolomic profiling of the autosomal dominant polycystic kidney disease rat model. Clinical and Experimental Nephrology, 15(5), 676-687. https://doi.org/10.1007/s10157-011-0467-4
Toyohara, Takafumi ; Suzuki, Takehiro ; Akiyama, Yasutoshi ; Yoshihara, Daisuke ; Takeuchi, Yoichi ; Mishima, Eikan ; Kikuchi, Koichi ; Suzuki, Chitose ; Tanemoto, Masayuki ; Ito, Sadayoshi ; Nagao, Shizuko ; Soga, Tomoyoshi ; Abe, Takaaki. / Metabolomic profiling of the autosomal dominant polycystic kidney disease rat model. :: Clinical and Experimental Nephrology. 2011 ; 巻 15, 番号 5. pp. 676-687.
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abstract = "Background: Autosomal dominant polycystic kidney disease (ADPKD) is an inherited systemic disease characterized by renal cyst expansion, resulting in renal failure. With the progression of renal damage, the accumulation of uremic compounds is recently reported to subsequently cause further renal damage and hypertension. Finding uremic toxins and sensitive markers for detecting the early stage of ADPKD is necessary to clarify its pathophysiological process and to prevent its progression. The aim of this study was to analyze the profile of uremic retention solutes of ADPKD by capillary electrophoresis-mass spectrometry (CE-MS) using the Han:SPRD rat model. Methods: Two hundred and ninety-seven cations and 190 anions were comprehensively analyzed by CE-MS in Han:SPRD rats and control rats. Results: We found 21 cations and 19 anions that accumulated significantly in the heterozygous (Cy/+) ADPKD rat model compared with control rats. Among the compounds, increases in 5-methyl-2′-deoxycytidine, glucosamine, ectoine, allantoate, α-hydroxybenzoate, phenaceturate and 3-phenylpropionate and decreases in 2-deoxycytidine, decanoate and 10-hydroxydecanoate were newly identified in the ADPKD Cy/+ rats. Conclusion: We identified uremic retention solutes in ADPKD Cy/+ rats. Compounds related to ADPKD could be useful markers for detecting the early stage of ADPKD.",
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Toyohara, T, Suzuki, T, Akiyama, Y, Yoshihara, D, Takeuchi, Y, Mishima, E, Kikuchi, K, Suzuki, C, Tanemoto, M, Ito, S, Nagao, S, Soga, T & Abe, T 2011, 'Metabolomic profiling of the autosomal dominant polycystic kidney disease rat model', Clinical and Experimental Nephrology, 巻. 15, 番号 5, pp. 676-687. https://doi.org/10.1007/s10157-011-0467-4

Metabolomic profiling of the autosomal dominant polycystic kidney disease rat model. / Toyohara, Takafumi; Suzuki, Takehiro; Akiyama, Yasutoshi; Yoshihara, Daisuke; Takeuchi, Yoichi; Mishima, Eikan; Kikuchi, Koichi; Suzuki, Chitose; Tanemoto, Masayuki; Ito, Sadayoshi; Nagao, Shizuko; Soga, Tomoyoshi; Abe, Takaaki.

:: Clinical and Experimental Nephrology, 巻 15, 番号 5, 01.10.2011, p. 676-687.

研究成果: Article

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T1 - Metabolomic profiling of the autosomal dominant polycystic kidney disease rat model

AU - Toyohara, Takafumi

AU - Suzuki, Takehiro

AU - Akiyama, Yasutoshi

AU - Yoshihara, Daisuke

AU - Takeuchi, Yoichi

AU - Mishima, Eikan

AU - Kikuchi, Koichi

AU - Suzuki, Chitose

AU - Tanemoto, Masayuki

AU - Ito, Sadayoshi

AU - Nagao, Shizuko

AU - Soga, Tomoyoshi

AU - Abe, Takaaki

PY - 2011/10/1

Y1 - 2011/10/1

N2 - Background: Autosomal dominant polycystic kidney disease (ADPKD) is an inherited systemic disease characterized by renal cyst expansion, resulting in renal failure. With the progression of renal damage, the accumulation of uremic compounds is recently reported to subsequently cause further renal damage and hypertension. Finding uremic toxins and sensitive markers for detecting the early stage of ADPKD is necessary to clarify its pathophysiological process and to prevent its progression. The aim of this study was to analyze the profile of uremic retention solutes of ADPKD by capillary electrophoresis-mass spectrometry (CE-MS) using the Han:SPRD rat model. Methods: Two hundred and ninety-seven cations and 190 anions were comprehensively analyzed by CE-MS in Han:SPRD rats and control rats. Results: We found 21 cations and 19 anions that accumulated significantly in the heterozygous (Cy/+) ADPKD rat model compared with control rats. Among the compounds, increases in 5-methyl-2′-deoxycytidine, glucosamine, ectoine, allantoate, α-hydroxybenzoate, phenaceturate and 3-phenylpropionate and decreases in 2-deoxycytidine, decanoate and 10-hydroxydecanoate were newly identified in the ADPKD Cy/+ rats. Conclusion: We identified uremic retention solutes in ADPKD Cy/+ rats. Compounds related to ADPKD could be useful markers for detecting the early stage of ADPKD.

AB - Background: Autosomal dominant polycystic kidney disease (ADPKD) is an inherited systemic disease characterized by renal cyst expansion, resulting in renal failure. With the progression of renal damage, the accumulation of uremic compounds is recently reported to subsequently cause further renal damage and hypertension. Finding uremic toxins and sensitive markers for detecting the early stage of ADPKD is necessary to clarify its pathophysiological process and to prevent its progression. The aim of this study was to analyze the profile of uremic retention solutes of ADPKD by capillary electrophoresis-mass spectrometry (CE-MS) using the Han:SPRD rat model. Methods: Two hundred and ninety-seven cations and 190 anions were comprehensively analyzed by CE-MS in Han:SPRD rats and control rats. Results: We found 21 cations and 19 anions that accumulated significantly in the heterozygous (Cy/+) ADPKD rat model compared with control rats. Among the compounds, increases in 5-methyl-2′-deoxycytidine, glucosamine, ectoine, allantoate, α-hydroxybenzoate, phenaceturate and 3-phenylpropionate and decreases in 2-deoxycytidine, decanoate and 10-hydroxydecanoate were newly identified in the ADPKD Cy/+ rats. Conclusion: We identified uremic retention solutes in ADPKD Cy/+ rats. Compounds related to ADPKD could be useful markers for detecting the early stage of ADPKD.

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Toyohara T, Suzuki T, Akiyama Y, Yoshihara D, Takeuchi Y, Mishima E その他. Metabolomic profiling of the autosomal dominant polycystic kidney disease rat model. Clinical and Experimental Nephrology. 2011 10 1;15(5):676-687. https://doi.org/10.1007/s10157-011-0467-4