Immunoneutralization of endogenous glucagon-like peptide-2 reduces adaptive intestinal growth in diabetic rats.

Research output: Contribution to journalJournal articleResearchpeer-review

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Immunoneutralization of endogenous glucagon-like peptide-2 reduces adaptive intestinal growth in diabetic rats. / Hartmann, Bolette; Thulesen, Jesper; Hare, Kristine Juul; Kissow, Hannelouise; Orskov, Cathrine; Poulsen, Steen Seier; Holst, Jens Juul.

In: Regulatory Peptides, Vol. 105, No. 3, 2002, p. 173-9.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Hartmann, B, Thulesen, J, Hare, KJ, Kissow, H, Orskov, C, Poulsen, SS & Holst, JJ 2002, 'Immunoneutralization of endogenous glucagon-like peptide-2 reduces adaptive intestinal growth in diabetic rats.', Regulatory Peptides, vol. 105, no. 3, pp. 173-9.

APA

Hartmann, B., Thulesen, J., Hare, K. J., Kissow, H., Orskov, C., Poulsen, S. S., & Holst, J. J. (2002). Immunoneutralization of endogenous glucagon-like peptide-2 reduces adaptive intestinal growth in diabetic rats. Regulatory Peptides, 105(3), 173-9.

Vancouver

Hartmann B, Thulesen J, Hare KJ, Kissow H, Orskov C, Poulsen SS et al. Immunoneutralization of endogenous glucagon-like peptide-2 reduces adaptive intestinal growth in diabetic rats. Regulatory Peptides. 2002;105(3):173-9.

Author

Hartmann, Bolette ; Thulesen, Jesper ; Hare, Kristine Juul ; Kissow, Hannelouise ; Orskov, Cathrine ; Poulsen, Steen Seier ; Holst, Jens Juul. / Immunoneutralization of endogenous glucagon-like peptide-2 reduces adaptive intestinal growth in diabetic rats. In: Regulatory Peptides. 2002 ; Vol. 105, No. 3. pp. 173-9.

Bibtex

@article{9f228310ab5211ddb5e9000ea68e967b,
title = "Immunoneutralization of endogenous glucagon-like peptide-2 reduces adaptive intestinal growth in diabetic rats.",
abstract = "Supraphysiological doses of glucagon-like peptide-2 (GLP-2) have been shown to induce intestinal growth by increasing villus height and crypt depth and by decreasing apoptosis, but a physiological effect of GLP-2 has not yet been demonstrated. Earlier, we found elevated levels of endogenous GLP-2 in untreated streptozotocin diabetic rats associated with marked intestinal growth. In the present study, we investigated the role of endogenous GLP-2 for this adaptive response. We included four groups of six rats: (1) diabetic rats treated with saline, (2) diabetic rats treated with non-specific antibodies, (3) diabetic rats treated with polyclonal GLP-2 antibodies and (4) non-diabetic control rats treated with saline. All animals were treated with once daily intraperitoneal injections for 13 days and killed on day 14. Diabetic rats treated with saline or non-specific antibodies had a significantly (P<0.01) increased area of mucosa (13.00+/-0.64 and 13.37+/-0.60 mm(2), respectively) in the proximal part of the small intestine compared with non-diabetic controls (7.97+/-0.70 mm(2)). In contrast, diabetic rats treated with GLP-2 antibodies had a significantly (P<0.01) smaller increase in area of mucosa in the proximal part of the small intestine (10.84+/-0.44 mm(2)). Antibody treatment had no effect on body weight, blood glucose concentrations and food intake. Thus, blocking of endogenous GLP-2 in a model of adaptive intestinal growth reduces the growth response, providing strong evidence for a physiological growth factor function of GLP-2.",
author = "Bolette Hartmann and Jesper Thulesen and Hare, {Kristine Juul} and Hannelouise Kissow and Cathrine Orskov and Poulsen, {Steen Seier} and Holst, {Jens Juul}",
note = "Keywords: Animals; Blood Glucose; Body Weight; Diabetes Mellitus; Eating; Female; Glucagon-Like Peptide 2; Glucagon-Like Peptides; Intestines; Neutralization Tests; Organ Size; Peptides; Rats; Rats, Wistar",
year = "2002",
language = "English",
volume = "105",
pages = "173--9",
journal = "Regulatory Peptides",
issn = "0167-0115",
publisher = "Elsevier",
number = "3",

}

RIS

TY - JOUR

T1 - Immunoneutralization of endogenous glucagon-like peptide-2 reduces adaptive intestinal growth in diabetic rats.

AU - Hartmann, Bolette

AU - Thulesen, Jesper

AU - Hare, Kristine Juul

AU - Kissow, Hannelouise

AU - Orskov, Cathrine

AU - Poulsen, Steen Seier

AU - Holst, Jens Juul

N1 - Keywords: Animals; Blood Glucose; Body Weight; Diabetes Mellitus; Eating; Female; Glucagon-Like Peptide 2; Glucagon-Like Peptides; Intestines; Neutralization Tests; Organ Size; Peptides; Rats; Rats, Wistar

PY - 2002

Y1 - 2002

N2 - Supraphysiological doses of glucagon-like peptide-2 (GLP-2) have been shown to induce intestinal growth by increasing villus height and crypt depth and by decreasing apoptosis, but a physiological effect of GLP-2 has not yet been demonstrated. Earlier, we found elevated levels of endogenous GLP-2 in untreated streptozotocin diabetic rats associated with marked intestinal growth. In the present study, we investigated the role of endogenous GLP-2 for this adaptive response. We included four groups of six rats: (1) diabetic rats treated with saline, (2) diabetic rats treated with non-specific antibodies, (3) diabetic rats treated with polyclonal GLP-2 antibodies and (4) non-diabetic control rats treated with saline. All animals were treated with once daily intraperitoneal injections for 13 days and killed on day 14. Diabetic rats treated with saline or non-specific antibodies had a significantly (P<0.01) increased area of mucosa (13.00+/-0.64 and 13.37+/-0.60 mm(2), respectively) in the proximal part of the small intestine compared with non-diabetic controls (7.97+/-0.70 mm(2)). In contrast, diabetic rats treated with GLP-2 antibodies had a significantly (P<0.01) smaller increase in area of mucosa in the proximal part of the small intestine (10.84+/-0.44 mm(2)). Antibody treatment had no effect on body weight, blood glucose concentrations and food intake. Thus, blocking of endogenous GLP-2 in a model of adaptive intestinal growth reduces the growth response, providing strong evidence for a physiological growth factor function of GLP-2.

AB - Supraphysiological doses of glucagon-like peptide-2 (GLP-2) have been shown to induce intestinal growth by increasing villus height and crypt depth and by decreasing apoptosis, but a physiological effect of GLP-2 has not yet been demonstrated. Earlier, we found elevated levels of endogenous GLP-2 in untreated streptozotocin diabetic rats associated with marked intestinal growth. In the present study, we investigated the role of endogenous GLP-2 for this adaptive response. We included four groups of six rats: (1) diabetic rats treated with saline, (2) diabetic rats treated with non-specific antibodies, (3) diabetic rats treated with polyclonal GLP-2 antibodies and (4) non-diabetic control rats treated with saline. All animals were treated with once daily intraperitoneal injections for 13 days and killed on day 14. Diabetic rats treated with saline or non-specific antibodies had a significantly (P<0.01) increased area of mucosa (13.00+/-0.64 and 13.37+/-0.60 mm(2), respectively) in the proximal part of the small intestine compared with non-diabetic controls (7.97+/-0.70 mm(2)). In contrast, diabetic rats treated with GLP-2 antibodies had a significantly (P<0.01) smaller increase in area of mucosa in the proximal part of the small intestine (10.84+/-0.44 mm(2)). Antibody treatment had no effect on body weight, blood glucose concentrations and food intake. Thus, blocking of endogenous GLP-2 in a model of adaptive intestinal growth reduces the growth response, providing strong evidence for a physiological growth factor function of GLP-2.

M3 - Journal article

C2 - 11959371

VL - 105

SP - 173

EP - 179

JO - Regulatory Peptides

JF - Regulatory Peptides

SN - 0167-0115

IS - 3

ER -

ID: 8418364