Effect of exendin (exenatide)-GLP1 receptor agonist on the thyroid and parathyroid gland in a rat model

被引:16
作者
Bulchandani, Deepti [1 ]
Nachnani, Jagdish S. [1 ]
Herndon, Betty [2 ]
Molteni, Agostino [2 ]
Pathan, Muhammad H. [2 ]
Quinn, Tim [2 ]
Hamdan, Hana A. [2 ]
Alba, Laura M. [2 ,3 ]
Graves, Leland [4 ]
机构
[1] Summer Med Grp, Gallatin, TN USA
[2] Univ Missouri Kansas City, Sch Med, Kansas City, KS USA
[3] St Lukes Hosp Kansas City, Kansas City, KS USA
[4] Univ Kansas, Sch Med, Lawrence, KS 66045 USA
关键词
Exendin-4; GLP-1; Thyroid; Parathyroid; Rat; GLUCAGON-LIKE PEPTIDE-1; CELLS; EXPRESSION; BIOLOGY; GLP-1;
D O I
10.1016/j.ejphar.2012.07.024
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Exenatide or Exendin-4 is a 39-amino acid agonist of the glucagon like peptide (GLP-1) receptor approved for the adjunctive treatment for type 2 diabetes. Recent reports suggest that GLP-1 agonists may also have distant effects including C-cell thyroid hyperplasia. The aim of this study was to evaluate the effect of exendin-4 on the thyroid and parathyroid cells in a rat model. Rat thyroids were stained for calcitonin, H&E and for carcinoembryonic antigen (CEA). Thyroid C-cell hyperplasia was graded on H&E stained slides using cell size and secretory granule numbers, morphological features of the parathyroid glands and the serum calcium concentrations of the rats were also evaluated. Counts of stained cells/high power field and intensity of staining were recorded by two pathologists. Data were analyzed by ANOVA/post-tests. C cell hypertrophy was elevated in exenatide-treated vs. untreated animals (22.5 perpendicular to 8.7 vs. 10.5 perpendicular to 2.7cells/HPF). CEA staining failed to show effects by exendin. Calcitonin staining was significantly elevated in exenatide treated controls (P<0.001). Parathyroid glands were histologically normal in both groups, and serum calcium levels were within normal range in all animals. In summary, exenatide was associated with C cell hyperplasia and increased calcitonin staining of thyroids, but was unrelated to CEA levels. These data raise important concerns about the effects of exenatide which, given its wide clinical use, should be clarified with urgency. Copyright (c) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:292 / 296
页数:5
相关论文
共 20 条
[1]   Insulinotropic hormone glucagon-like peptide-1 differentiation of human pancreatic islet-derived progenitor cells into insulin-producing cells [J].
Abraham, EJ ;
Leech, CA ;
Lin, JC ;
Zulewski, H ;
Habener, JF .
ENDOCRINOLOGY, 2002, 143 (08) :3152-3161
[2]  
Ahmad SR, 2008, NEW ENGL J MED, V358, P1970
[3]  
[Anonymous], 2008, LIRAGLUTIDE PACKAGE
[4]   Biology of incretins: GLP-1 and GIP [J].
Baggio, Laurie L. ;
Drucker, Daniel J. .
GASTROENTEROLOGY, 2007, 132 (06) :2131-2157
[5]   Cardioprotective and vasodilatory actions of glucagon-like peptide 1 receptor are mediated through both glucagon-like peptide 1 receptor-dependent and -independent pathways [J].
Ban, Kiwon ;
Noyan-Ashraf, M. Hossein ;
Hoefer, Judith ;
Bolz, Steffen-Sebastian ;
Drucker, Daniel J. ;
Husain, Mansoor .
CIRCULATION, 2008, 117 (18) :2340-2350
[6]   Glucagon-Like Peptide (GLP)-1(9-36)Amide-Mediated Cytoprotection Is Blocked by Exendin(9-39) Yet Does Not Require the Known GLP-1 Receptor [J].
Ban, Kiwon ;
Kim, Kyoung-Han ;
Cho, Chan-Kyung ;
Sauve, Meghan ;
Diamandis, Eleftherios P. ;
Backx, Peter H. ;
Drucker, Daniel J. ;
Husain, Mansoor .
ENDOCRINOLOGY, 2010, 151 (04) :1520-1531
[7]   Minireview: Update on Incretin Biology: Focus on Glucagon-Like Peptide-1 [J].
Brubaker, Patricia L. .
ENDOCRINOLOGY, 2010, 151 (05) :1984-1989
[8]   Role of glucagon-like peptide-1 in the pathogenesis and treatment of diabetes mellitus [J].
De León, DD ;
Crutchlow, MF ;
Ham, JYN ;
Stoffers, DA .
INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 2006, 38 (5-6) :845-859
[9]   Exenatide (Exendin-4)-induced pancreatitis - A case report [J].
Denker, PS ;
Dimarco, PE .
DIABETES CARE, 2006, 29 (02) :471-471
[10]  
GOKE R, 1993, J BIOL CHEM, V268, P19650