C-Peptide-Based Assessment of Insulin Secretion in the Zucker Fatty Rat: A Modelistic Study

被引:10
作者
Di Nardo, Francesco [1 ]
Cogo, Carla E. [2 ]
Faelli, Emanuela [2 ]
Morettini, Micaela [1 ]
Burattini, Laura [1 ]
Ruggeri, Piero [2 ]
机构
[1] Univ Politecn Marche, Dept Informat Engn, Ancona, Italy
[2] Univ Genoa, Dept Expt Med, Genoa, Italy
关键词
BETA-CELL FUNCTION; HEPATIC EXTRACTION; GLUCOSE-TOLERANCE; MINIMAL MODEL; SENSITIVITY; RESISTANCE; HUMANS; MECHANISMS; KINETICS;
D O I
10.1371/journal.pone.0125252
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
A C-peptide-based assessment of beta-cell function was performed here in the Zucker fatty rat, a suitable animal model of human metabolic syndrome. To this aim, a 90-min intravenous glucose tolerance test (IVGTT) was performed in seven Zucker fatty rats (ZFR), 7-to-9week-old, and seven age-matched Zucker lean rats (ZLR). The minimal model of Cpeptide (CPMM), originally introduced for humans, was adapted to Zucker rats and then applied to interpret IVGTT data. For a comprehensive evaluation of glucose tolerance in ZFR, CPMM was applied in combination with the minimal model of glucose kinetics (GKMM). Our results showed that the present CPMM-based interpretation of data is able to: 1) provide a suitable fit of C-Peptide data; 2) achieve a satisfactory estimation of parameters of interest 3) quantify both insulin secretion by estimating the time course of pre-hepatic secretion rate, SR(t), and total insulin secretion, TIS, and pancreatic sensitivity by means of three specific indexes of beta-cell responsiveness to glucose stimulus (first-phase,phi(1), second-phase,phi(2), and steady-state,phi(ss), never assessed in Zucker rats before; 4) detect the significant enhancement of insulin secretion in the ZFR, in face of a severe insulin-resistant state, previously observed only using a purely experimental approach. Thus, the methodology presented here represents a reliable tool to assess beta-cell function in the Zucker rat, and opens new possibilities for the quantification of further processes involved in glucose homeostasis such as the hepatic insulin degradation.
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页数:14
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