Abstract
A C-peptide-based assessment of β-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 C-peptide (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 β-cell responsiveness to glucose stimulus (first-phase, Ф1, second-phase, Ф2, and steady-state, Фss, 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 β-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.
Highlights
The Zucker fatty rat (ZFR) is a widely recognized experimental model of human obesity, insulin resistance and presents abnormalities similar to those observed in human metabolic syndrome [1,2,3,4,5]
For a comprehensive evaluation of glucose tolerance in ZFR, CPMM was applied in combination with the minimal model of glucose kinetics (GKMM)
Beyond direct measurements, which are hard to perform in small-sized animal, many empirical and model-based tools are available for the quantification of insulin action in the Zucker rat; in particular, our previous work confirmed the reliability of the minimal model of glucose kinetics (GKMM) in providing estimates of insulin sensitivity and glucose effectiveness [9,10]
Summary
The Zucker fatty rat (ZFR) is a widely recognized experimental model of human obesity, insulin resistance and presents abnormalities similar to those observed in human metabolic syndrome [1,2,3,4,5]. The usefulness of the ZFR as an experimental model of human metabolic dysfunctions implies the comprehensive evaluation of glucose tolerance by simultaneous quantification of physiological processes of insulin secretion, action and clearance. Beyond direct measurements, which are hard to perform in small-sized animal, many empirical and model-based tools are available for the quantification of insulin action in the Zucker rat; in particular, our previous work confirmed the reliability of the minimal model of glucose kinetics (GKMM) in providing estimates of insulin sensitivity and glucose effectiveness [9,10]
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