Volume 117, Issue 1, Pages (July 1999)

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Volume 117, Issue 1, Pages 99-105 (July 1999) Secretion of the intestinotropic hormone glucagon-like peptide 2 is differentially regulated by nutrients in humans  Qiang Xiao*, Robin P. Boushey‡, Daniel J. Drucker‡,§, Patricia L. Brubaker*,‡  Gastroenterology  Volume 117, Issue 1, Pages 99-105 (July 1999) DOI: 10.1016/S0016-5085(99)70555-X Copyright © 1999 American Gastroenterological Association Terms and Conditions

Fig. 1 Schematic representation of different GLP-2–containing peptides. The binding sites for antisera UTTH7 (circles) and #92160 (arrowhead) are indicated. Gastroenterology 1999 117, 99-105DOI: (10.1016/S0016-5085(99)70555-X) Copyright © 1999 American Gastroenterological Association Terms and Conditions

Fig. 2 Changes in plasma concentrations of N-IR-GLP-2 (•) and T-IR-GLP-2 (▴) over a 24-hour period with a normal 2500-kcal diet (51.3% carbohydrate, 29.3% fat, and 19.5% protein) in normal fasted human volunteers (n = 6). The arrows indicate feeding times of breakfast (B; 549 kcal), lunch (L; 582 kcal), dinner (D; 742 kcal), and snacks (S; 135–351 kcal). All studies started at 9 AM. Plasma samples were extracted before RIA. Gastroenterology 1999 117, 99-105DOI: (10.1016/S0016-5085(99)70555-X) Copyright © 1999 American Gastroenterological Association Terms and Conditions

Fig. 3 (A) Changes in plasma concentrations of N-IR-GLP-2 (•) and T-IR-GLP-2 (▴) over a 4-hour period with a 400-kcal (300 mL) carbohydrate breakfast in normal fasted human volunteers (n = 6). All studies started at 9 AM. Plasma samples were extracted before RIA. (B) Individual N-IR-GLP-2 responses, with different symbols used for each volunteer. Gastroenterology 1999 117, 99-105DOI: (10.1016/S0016-5085(99)70555-X) Copyright © 1999 American Gastroenterological Association Terms and Conditions

Fig. 4 (A) Changes in plasma concentrations of N-IR-GLP-2 (•) and T-IR-GLP-2 (▴) over a 4-hour period with a 400-kcal (300 mL) fat breakfast in normal fasted human volunteers (n = 4–6). All studies started at 9 AM. Plasma samples were extracted before RIA. (B) Individual N-IR-GLP-2 responses, with different symbols used for each volunteer (as in Figure 3). Gastroenterology 1999 117, 99-105DOI: (10.1016/S0016-5085(99)70555-X) Copyright © 1999 American Gastroenterological Association Terms and Conditions

Fig. 5 (A) Changes in plasma concentrations of N-IR-GLP-2 (•) and T-IR-GLP-2 (▴) over a 4-hour period with a 400-kcal (300 mL) protein breakfast in normal fasted human volunteers (n = 6). All studies started at 9 AM. Plasma samples were extracted before RIA. (B) Individual N-IR-GLP-2 responses, with different symbols used for each volunteer (as in Figure 3). Gastroenterology 1999 117, 99-105DOI: (10.1016/S0016-5085(99)70555-X) Copyright © 1999 American Gastroenterological Association Terms and Conditions

Fig. 6 HPLC profiles of fasting (basal) and peak (stimulated) plasma samples (2 mL each) from normal fasted human volunteers fed a 400-kcal (300 mL) fat breakfast. The profiles shown are representative of 2 fat and 2 carbohydrate meals. Plasma samples were extracted before HPLC, and fractions were subjected to RIA for T-IR-GLP-2. Gastroenterology 1999 117, 99-105DOI: (10.1016/S0016-5085(99)70555-X) Copyright © 1999 American Gastroenterological Association Terms and Conditions