Glucagon-like peptide 2 has limited efficacy to increase nutrient absorption in fetal and preterm pigs

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Standard

Glucagon-like peptide 2 has limited efficacy to increase nutrient absorption in fetal and preterm pigs. / Sangild, Per Torp; Malo, Christiane; Schmidt, Mette; Petersen, Yvette M.; Elnif, Jan; Holst, Jens Juul; Bunddington, Randal K.

I: American Journal of Physiology: Regulatory, Integrative and Comparative Physiology, Bind 293, Nr. 6, 2007, s. R2179-R2184.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Sangild, PT, Malo, C, Schmidt, M, Petersen, YM, Elnif, J, Holst, JJ & Bunddington, RK 2007, 'Glucagon-like peptide 2 has limited efficacy to increase nutrient absorption in fetal and preterm pigs', American Journal of Physiology: Regulatory, Integrative and Comparative Physiology, bind 293, nr. 6, s. R2179-R2184. https://doi.org/10.1152/ajpregu.00395.2007

APA

Sangild, P. T., Malo, C., Schmidt, M., Petersen, Y. M., Elnif, J., Holst, J. J., & Bunddington, R. K. (2007). Glucagon-like peptide 2 has limited efficacy to increase nutrient absorption in fetal and preterm pigs. American Journal of Physiology: Regulatory, Integrative and Comparative Physiology, 293(6), R2179-R2184. https://doi.org/10.1152/ajpregu.00395.2007

Vancouver

Sangild PT, Malo C, Schmidt M, Petersen YM, Elnif J, Holst JJ o.a. Glucagon-like peptide 2 has limited efficacy to increase nutrient absorption in fetal and preterm pigs. American Journal of Physiology: Regulatory, Integrative and Comparative Physiology. 2007;293(6):R2179-R2184. https://doi.org/10.1152/ajpregu.00395.2007

Author

Sangild, Per Torp ; Malo, Christiane ; Schmidt, Mette ; Petersen, Yvette M. ; Elnif, Jan ; Holst, Jens Juul ; Bunddington, Randal K. / Glucagon-like peptide 2 has limited efficacy to increase nutrient absorption in fetal and preterm pigs. I: American Journal of Physiology: Regulatory, Integrative and Comparative Physiology. 2007 ; Bind 293, Nr. 6. s. R2179-R2184.

Bibtex

@article{622f61f0a1c311ddb6ae000ea68e967b,
title = "Glucagon-like peptide 2 has limited efficacy to increase nutrient absorption in fetal and preterm pigs",
abstract = "Exogenous glucagon-like peptide 2 (GLP-2) prevents intestinal atrophy and increases nutrient absorption in term newborn pigs receiving total parenteral nutrition (TPN). We tested the hypothesis that the immature intestine of fetuses and preterm neonates has a diminished nutrient absorption response to exogenous GLP-2. This was accomplished using catheterized fetal pigs infused for 6 days (87-91% of gestation) with GLP-2 (25 nmol.kg(-1).day(-1) iv; n = 7) or saline (n = 7), and cesarean-delivered preterm pigs (92% of gestation) that received TPN with GLP-2 (25 nmol.kg(-1).day(-1) iv; n = 8) or saline (n = 7) for 6 days after birth. Responses to GLP-2 were assessed by measuring intestinal dimensions, absorption of nutrients (glucose, leucine, lysine, proline) by intact tissues and brush border membrane vesicles, and abundance of sodium-glucose cotransporter mRNA. Infusion of GLP-2 increased circulating GLP-2 levels in fetuses, but did not increase intestinal mass or absorption of nutrients by intact tissues and brush border membrane vesicles, except for lysine. Administration of exogenous GLP-2 to preterm TPN-fed pigs similarly did not increase rates of nutrient absorption, yet nutrient absorption capacities of the entire small intestine tended to increase (+10-20%, P < 0.10) compared with TPN alone due to increased intestinal mass (+30%, P < 0.05). GLP-2 infusion did not increase sodium-glucose cotransporter-1 mRNA abundance in fetuses or postnatal preterm pigs. Hence, the efficacy of exogenous GLP-2 to improve nutrient absorption by the intestine of fetal and preterm pigs is limited compared with term pigs and more mature animals and humans.",
author = "Sangild, {Per Torp} and Christiane Malo and Mette Schmidt and Petersen, {Yvette M.} and Jan Elnif and Holst, {Jens Juul} and Bunddington, {Randal K.}",
year = "2007",
doi = "10.1152/ajpregu.00395.2007",
language = "English",
volume = "293",
pages = "R2179--R2184",
journal = "American Journal of Physiology",
issn = "0363-6119",
publisher = "American Physiological Society",
number = "6",

}

RIS

TY - JOUR

T1 - Glucagon-like peptide 2 has limited efficacy to increase nutrient absorption in fetal and preterm pigs

AU - Sangild, Per Torp

AU - Malo, Christiane

AU - Schmidt, Mette

AU - Petersen, Yvette M.

AU - Elnif, Jan

AU - Holst, Jens Juul

AU - Bunddington, Randal K.

PY - 2007

Y1 - 2007

N2 - Exogenous glucagon-like peptide 2 (GLP-2) prevents intestinal atrophy and increases nutrient absorption in term newborn pigs receiving total parenteral nutrition (TPN). We tested the hypothesis that the immature intestine of fetuses and preterm neonates has a diminished nutrient absorption response to exogenous GLP-2. This was accomplished using catheterized fetal pigs infused for 6 days (87-91% of gestation) with GLP-2 (25 nmol.kg(-1).day(-1) iv; n = 7) or saline (n = 7), and cesarean-delivered preterm pigs (92% of gestation) that received TPN with GLP-2 (25 nmol.kg(-1).day(-1) iv; n = 8) or saline (n = 7) for 6 days after birth. Responses to GLP-2 were assessed by measuring intestinal dimensions, absorption of nutrients (glucose, leucine, lysine, proline) by intact tissues and brush border membrane vesicles, and abundance of sodium-glucose cotransporter mRNA. Infusion of GLP-2 increased circulating GLP-2 levels in fetuses, but did not increase intestinal mass or absorption of nutrients by intact tissues and brush border membrane vesicles, except for lysine. Administration of exogenous GLP-2 to preterm TPN-fed pigs similarly did not increase rates of nutrient absorption, yet nutrient absorption capacities of the entire small intestine tended to increase (+10-20%, P < 0.10) compared with TPN alone due to increased intestinal mass (+30%, P < 0.05). GLP-2 infusion did not increase sodium-glucose cotransporter-1 mRNA abundance in fetuses or postnatal preterm pigs. Hence, the efficacy of exogenous GLP-2 to improve nutrient absorption by the intestine of fetal and preterm pigs is limited compared with term pigs and more mature animals and humans.

AB - Exogenous glucagon-like peptide 2 (GLP-2) prevents intestinal atrophy and increases nutrient absorption in term newborn pigs receiving total parenteral nutrition (TPN). We tested the hypothesis that the immature intestine of fetuses and preterm neonates has a diminished nutrient absorption response to exogenous GLP-2. This was accomplished using catheterized fetal pigs infused for 6 days (87-91% of gestation) with GLP-2 (25 nmol.kg(-1).day(-1) iv; n = 7) or saline (n = 7), and cesarean-delivered preterm pigs (92% of gestation) that received TPN with GLP-2 (25 nmol.kg(-1).day(-1) iv; n = 8) or saline (n = 7) for 6 days after birth. Responses to GLP-2 were assessed by measuring intestinal dimensions, absorption of nutrients (glucose, leucine, lysine, proline) by intact tissues and brush border membrane vesicles, and abundance of sodium-glucose cotransporter mRNA. Infusion of GLP-2 increased circulating GLP-2 levels in fetuses, but did not increase intestinal mass or absorption of nutrients by intact tissues and brush border membrane vesicles, except for lysine. Administration of exogenous GLP-2 to preterm TPN-fed pigs similarly did not increase rates of nutrient absorption, yet nutrient absorption capacities of the entire small intestine tended to increase (+10-20%, P < 0.10) compared with TPN alone due to increased intestinal mass (+30%, P < 0.05). GLP-2 infusion did not increase sodium-glucose cotransporter-1 mRNA abundance in fetuses or postnatal preterm pigs. Hence, the efficacy of exogenous GLP-2 to improve nutrient absorption by the intestine of fetal and preterm pigs is limited compared with term pigs and more mature animals and humans.

U2 - 10.1152/ajpregu.00395.2007

DO - 10.1152/ajpregu.00395.2007

M3 - Journal article

C2 - 17898120

VL - 293

SP - R2179-R2184

JO - American Journal of Physiology

JF - American Journal of Physiology

SN - 0363-6119

IS - 6

ER -

ID: 8093071