A decrease in plasma glucose levels is required for increased endogenous glucose production with a single administration of a sodium‐glucose co‐transporter‐2 inhibitor tofogliflozin
A decrease in plasma glucose levels is required for increased endogenous glucose production with a single administration of a sodium‐glucose co‐transporter‐2 inhibitor tofogliflozin
复制标题
单次服用钠-葡萄糖协同转运蛋白-2抑制剂托格列净需要降低血浆葡萄糖水平,以增加内源性葡萄糖的产生
DOI:
10.1111/dom.14312
复制
发表时间:
2021
期刊:
影响因子:
--
通讯作者:
Watada H
中科院分区:
文献类型:
--
作者:
Yamasaki;Tamura Y;Kaga H;Sato M;Kiya M;Kadowaki S;Suzuki R;Furukawa Y;Sugimoto D;Funayama T;Someya Y;Kakehi S;Nojiri S;Satoh H;Kawamori R;Watada H
Aim: To investigate whether changes in endogenous glucose production (EGP) and insulin and glucagon levels are elicited by the decrease in plasma glucose (PG) levels induced by the sodium-glucose co-transporter-2 (SGLT2) inhibitor tofogliflozin. Materials and methods: We evaluated EGP in 12 Japanese patients with type 2 diabetes under 60 the conditions of no drugs administered (CON), single administration of the SGLT2i tofogliflozin (TOF), and single administration of TOF with adjustment of PG levels with exogenous glucose infusion to mimic changes in PG levels observed with CON (TOF+ G). We evaluated changes in EGP and levels of C-peptide and glucagon from baseline to 180 min after drug administration. 65Results: Endogenous glucose production decreased in CON (-0.22±0.11 mg/kg· min) and TOF+ G (-0.31±0.24 mg/kg· min), but not in TOF (+ 0.08±0.19 mg/kg· min). The decrease in C-peptide was significantly greater in TOF (-0.11±0.06 nmol/L) than in CON (-0.03±0.06 nmol/L) and TOF+ G (-0.01±0.11 nmol/L), while the increase in glucagon was significantly greater in TOF (+ 11.1±6.3 pmol/L) but not TOF+ G (+ 8.6±7.6 pmol/L) than in CON (+ 5.1±4.3 70 pmol/L).Conclusions: These results indicate that the decrease in PG levels induced by SGLT2 inhibitor administration is required for the increase in EGP and decrease in insulin secretion.
登录
查看更多内容
DOI:
10.1016/0026-0495(90)90192-f
发表时间:
1990
期刊:
Metabolism: clinical and experimental
影响因子:
--
作者:
K. Steiner;P. Williams;W. Lacy;A. Cherrington
通讯作者:
A. Cherrington
影响因子:
158.5
作者:
Wiviott, S. D.;Raz, I.;Sabatine, M. S.
通讯作者:
Sabatine, M. S.
影响因子:
--
作者:
A. Cherrington;R. W. Stevenson;K. Steiner;C. C. Connolly;M. Wada;R. Goldstein
通讯作者:
R. Goldstein
DOI:
10.1152/ajpendo.00117.2003
发表时间:
2003-10-01
影响因子:
5.1
作者:
Kelley, DE;McKolanis, TM;Kalhan, SC
通讯作者:
Kalhan, SC
影响因子:
82.9
作者:
Bonner, Caroline;Kerr-Conte, Julie;Pattou, Francois
通讯作者:
Pattou, Francois