TY - JOUR
T1 - Evaluation of serum arginase I as an oxidative stress biomarker in a healthy Japanese population using a newly established ELISA
AU - Ogino, Keiki
AU - Murakami, Ikuo
AU - Wang, Da Hong
AU - Tsukiyama, Yorika
AU - Takahashi, Hidekazu
AU - Kubo, Masayuki
AU - Sakano, Noriko
AU - Setiawan, Heri
AU - Bando, Masahiko
AU - Ohmoto, Yasukazu
N1 - Funding Information:
This work was supported in part by a Grant-in-Aid for Scientific Research (no. 23390163 ) from the Ministry of Education, Culture, Sports, Science and Technology of the Japanese Government .
Funding Information:
Keiki Ogino has received grant support from Otsuka Pharmaceutical Co., Ltd . Ikuo Murakami, Masahiko Bando, and Yasukazu Ohmoto are employed by Otsuka Pharmaceutical Co., Ltd.
PY - 2013/11
Y1 - 2013/11
N2 - Objective: We reported previously that serum arginase I increased in asthmatic patients and was associated with oxidative stress in a small healthy population. However, the exact association of arginase I with oxidative stress is not known. The present study aimed to analyze the association of arginase I with oxidative stress in a larger healthy population by a newly established ELISA. Design and methods: The new ELISA for the measurement of human arginase I was established by generating recombinant arginase I protein in human arginase I gene-transfected Escherichia coli via an ARG1 cDNA fragment-inserted vector and -specific antibody in rabbits. Serum arginase I was evaluated in a cross-sectional study on a healthy population (n. = 721) by comparing a commercial ELISA kit with the new ELISA. Results: The mean levels of serum arginase I were 20.3. ±. 0.7. ng/mL and 4.7. ±. 0.2. ng/mL using the commercial ELISA kit and the new ELISA, respectively. Arginase I was correlated with WBC, RBC, hs-CRP, 8-OHdG, HDL-c, ALT, and BMI. Logistic regression analysis showed independent positive associations of arginase I with WBC, RBC, and urinary 8-OHdG and inverse independent associations with serum insulin and age. The association of arginase I with hs-CRP was not independent. Conclusion: The independent associations of arginase I with urinary 8-OHdG and serum insulin may reflect its involvement in oxidative stress and diabetes mellitus.
AB - Objective: We reported previously that serum arginase I increased in asthmatic patients and was associated with oxidative stress in a small healthy population. However, the exact association of arginase I with oxidative stress is not known. The present study aimed to analyze the association of arginase I with oxidative stress in a larger healthy population by a newly established ELISA. Design and methods: The new ELISA for the measurement of human arginase I was established by generating recombinant arginase I protein in human arginase I gene-transfected Escherichia coli via an ARG1 cDNA fragment-inserted vector and -specific antibody in rabbits. Serum arginase I was evaluated in a cross-sectional study on a healthy population (n. = 721) by comparing a commercial ELISA kit with the new ELISA. Results: The mean levels of serum arginase I were 20.3. ±. 0.7. ng/mL and 4.7. ±. 0.2. ng/mL using the commercial ELISA kit and the new ELISA, respectively. Arginase I was correlated with WBC, RBC, hs-CRP, 8-OHdG, HDL-c, ALT, and BMI. Logistic regression analysis showed independent positive associations of arginase I with WBC, RBC, and urinary 8-OHdG and inverse independent associations with serum insulin and age. The association of arginase I with hs-CRP was not independent. Conclusion: The independent associations of arginase I with urinary 8-OHdG and serum insulin may reflect its involvement in oxidative stress and diabetes mellitus.
KW - Arginase I
KW - ELISA
KW - Oxidative stress
KW - Population study
UR - http://www.scopus.com/inward/record.url?scp=84886390546&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84886390546&partnerID=8YFLogxK
U2 - 10.1016/j.clinbiochem.2013.08.012
DO - 10.1016/j.clinbiochem.2013.08.012
M3 - Article
C2 - 24005081
AN - SCOPUS:84886390546
SN - 0009-9120
VL - 46
SP - 1717
EP - 1722
JO - Clinical Biochemistry
JF - Clinical Biochemistry
IS - 16-17
ER -