TY - JOUR
T1 - Long-term dietary nitrite and nitrate deficiency causes the metabolic syndrome, endothelial dysfunction and cardiovascular death in mice
AU - Kina-Tanada, Mika
AU - Sakanashi, Mayuko
AU - Tanimoto, Akihide
AU - Kaname, Tadashi
AU - Matsuzaki, Toshihiro
AU - Noguchi, Katsuhiko
AU - Uchida, Taro
AU - Nakasone, Junko
AU - Kozuka, Chisayo
AU - Ishida, Masayoshi
AU - Kubota, Haruaki
AU - Taira, Yuji
AU - Totsuka, Yuichi
AU - Kina, Shin ichiro
AU - Sunakawa, Hajime
AU - Omura, Junichi
AU - Satoh, Kimio
AU - Shimokawa, Hiroaki
AU - Yanagihara, Nobuyuki
AU - Maeda, Shiro
AU - Ohya, Yusuke
AU - Matsushita, Masayuki
AU - Masuzaki, Hiroaki
AU - Arasaki, Akira
AU - Tsutsui, Masato
N1 - Funding Information:
This work was supported in part by Grant-in-Aids for Research Activity Start-up (15H06519) and Scientific Research (C) (16K09519) from the Japan Society for the Promotion of Science, Special Account Budgets for Education and Research granted by the Japan Ministry of Education, and Grants from the Okinawa Medical Science Research Foundation, the Ryukyu University Support Foundation, the Promotion Project of Medical Clustering of Okinawa Prefecture, the Okinawa Prefecture for Promotion of Advanced Medicine and the University of the Ryukyus, Japan.
Publisher Copyright:
© 2017, Springer-Verlag Berlin Heidelberg.
PY - 2017/6/1
Y1 - 2017/6/1
N2 - Aims/hypothesis: Nitric oxide (NO) is synthesised not only from l-arginine by NO synthases (NOSs), but also from its inert metabolites, nitrite and nitrate. Green leafy vegetables are abundant in nitrate, but whether or not a deficiency in dietary nitrite/nitrate spontaneously causes disease remains to be clarified. In this study, we tested our hypothesis that long-term dietary nitrite/nitrate deficiency would induce the metabolic syndrome in mice. Methods: To this end, we prepared a low-nitrite/nitrate diet (LND) consisting of an amino acid-based low-nitrite/nitrate chow, in which the contents of l-arginine, fat, carbohydrates, protein and energy were identical with a regular chow, and potable ultrapure water. Nitrite and nitrate were undetectable in both the chow and the water. Results: Three months of the LND did not affect food or water intake in wild-type C57BL/6J mice compared with a regular diet (RD). However, in comparison with the RD, 3 months of the LND significantly elicited visceral adiposity, dyslipidaemia and glucose intolerance. Eighteen months of the LND significantly provoked increased body weight, hypertension, insulin resistance and impaired endothelium-dependent relaxations to acetylcholine, while 22 months of the LND significantly led to death mainly due to cardiovascular disease, including acute myocardial infarction. These abnormalities were reversed by simultaneous treatment with sodium nitrate, and were significantly associated with endothelial NOS downregulation, adiponectin insufficiency and dysbiosis of the gut microbiota. Conclusions/interpretation: These results provide the first evidence that long-term dietary nitrite/nitrate deficiency gives rise to the metabolic syndrome, endothelial dysfunction and cardiovascular death in mice, indicating a novel pathogenetic role of the exogenous NO production system in the metabolic syndrome and its vascular complications.
AB - Aims/hypothesis: Nitric oxide (NO) is synthesised not only from l-arginine by NO synthases (NOSs), but also from its inert metabolites, nitrite and nitrate. Green leafy vegetables are abundant in nitrate, but whether or not a deficiency in dietary nitrite/nitrate spontaneously causes disease remains to be clarified. In this study, we tested our hypothesis that long-term dietary nitrite/nitrate deficiency would induce the metabolic syndrome in mice. Methods: To this end, we prepared a low-nitrite/nitrate diet (LND) consisting of an amino acid-based low-nitrite/nitrate chow, in which the contents of l-arginine, fat, carbohydrates, protein and energy were identical with a regular chow, and potable ultrapure water. Nitrite and nitrate were undetectable in both the chow and the water. Results: Three months of the LND did not affect food or water intake in wild-type C57BL/6J mice compared with a regular diet (RD). However, in comparison with the RD, 3 months of the LND significantly elicited visceral adiposity, dyslipidaemia and glucose intolerance. Eighteen months of the LND significantly provoked increased body weight, hypertension, insulin resistance and impaired endothelium-dependent relaxations to acetylcholine, while 22 months of the LND significantly led to death mainly due to cardiovascular disease, including acute myocardial infarction. These abnormalities were reversed by simultaneous treatment with sodium nitrate, and were significantly associated with endothelial NOS downregulation, adiponectin insufficiency and dysbiosis of the gut microbiota. Conclusions/interpretation: These results provide the first evidence that long-term dietary nitrite/nitrate deficiency gives rise to the metabolic syndrome, endothelial dysfunction and cardiovascular death in mice, indicating a novel pathogenetic role of the exogenous NO production system in the metabolic syndrome and its vascular complications.
KW - Acute myocardial infarction
KW - Cardiovascular death
KW - Diet
KW - Endothelial dysfunction
KW - Metabolic syndrome
KW - Mice
KW - Nitrate
KW - Nitric oxide
KW - Nitrite
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U2 - 10.1007/s00125-017-4259-6
DO - 10.1007/s00125-017-4259-6
M3 - Article
C2 - 28352942
AN - SCOPUS:85016090848
VL - 60
SP - 1138
EP - 1151
JO - Diabetologia
JF - Diabetologia
SN - 0012-186X
IS - 6
ER -