| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Ryuya Maekawa, Hidetada Ogata, Masatoshi Murase, Norio Harada, Kazuyo Suzuki, Erina Joo, Akiko Sankoda, Atsushi Iida, Takako Izumoto, Shin Tsunekawa, Yoji Hamada, Yutaka Oiso, Nobuya Inagaki, Hiroshi Arima, Yoshitaka Hayashi, Yusuke Sein. Glucose-dependent insulinotropic polypeptide is required for moderate high-fat diet- but not high-carbohydrate diet-induced weight gain. American journal of physiology. Endocrinology and metabolism. vol 314. issue 6. 2019-02-19. PMID:29406782. |
in this study, we analyzed the effect of st feeding on gip secretion and metabolic parameters to explore the role of gip in st-induced weight gain. |
2019-02-19 |
2023-08-13 |
mouse |
| Chee W Chia, Michelle Shardell, Kristofer S Gravenstein, Olga D Carlson, Eleanor M Simonsick, Luigi Ferrucci, Josephine M Ega. Regular low-calorie sweetener consumption is associated with increased secretion of glucose-dependent insulinotropic polypeptide. Diabetes, obesity & metabolism. vol 20. issue 9. 2019-02-05. PMID:29687583. |
regular consumption of lcss was associated with greater increases in gip secretion after food intake, which may potentially lead to weight gain through the lipogenic properties of gip. |
2019-02-05 |
2023-08-13 |
human |
| K E McCool, A J Rudinsky, V J Parker, C O Herbert, C Gilo. The effect of diet, adiposity, and weight loss on the secretion of incretin hormones in cats. Domestic animal endocrinology. vol 62. 2018-07-20. PMID:29128557. |
glucose, insulin, glucagon-like peptide-1 (glp-1), and glucose-dependent insulinotropic peptide (gip) concentrations were measured immediately before and over 6 h after feeding the smt. |
2018-07-20 |
2023-08-13 |
mouse |
| Jie Zhang, Hui Jia, Qingqing Wang, Yajie Zhang, Wenda Wu, Haibin Zhan. Role of Peptide YY3-36 and Glucose-Dependent Insulinotropic Polypeptide in Anorexia Induction by Trichothecences T-2 Toxin, HT-2 Toxin, Diacetoxyscirpenol, and Neosolaniol. Toxicological sciences : an official journal of the Society of Toxicology. vol 159. issue 1. 2018-06-19. PMID:28666375. |
oral exposure to or intraperitoneal (ip) injection of 1 mg/kg bw t-2, ht-2, das, or neo resulted in dramatically decreased food intake, and pyy3-36 and gip concentrations were elevated accordingly. |
2018-06-19 |
2023-08-13 |
mouse |
| H Shoji, A Watanabe, N Ikeda, M Mori, T Kitamura, K Hisata, T Shimiz. Influence of gestational age on serum incretin levels in preterm infants. Journal of developmental origins of health and disease. vol 7. issue 6. 2017-11-21. PMID:27451916. |
glucose-dependent insulinotropic polypeptide (gip) and glucagon-like peptide-1 (glp-1) are the incretin hormones secreted from the intestine in response to enteral feeding to stimulate insulin secretion. |
2017-11-21 |
2023-08-13 |
Not clear |
| Rebecka Hammersjö, Bodil Roth, Peter Höglund, Bodil Ohlsso. Esophageal and Gastric Dysmotilities are Associated with Altered Glucose Homeostasis and Plasma Levels of Incretins and Leptin. The review of diabetic studies : RDS. vol 13. issue 1. 2017-11-03. PMID:27563696. |
glucose-dependent insulinotropic peptide (gip), glucagon-like peptide-1 (glp-1), and leptin regulate glucose homeostasis, food intake, and gastric emptying. |
2017-11-03 |
2023-08-13 |
Not clear |
| Cherl NamKoong, Min Sun Kim, Byeong-Tak Jang, Young Hee Lee, Young-Min Cho, Hyung Jin Cho. Central administration of GLP-1 and GIP decreases feeding in mice. Biochemical and biophysical research communications. vol 490. issue 2. 2017-09-26. PMID:28610922. |
central administration of glp-1 and gip decreases feeding in mice. |
2017-09-26 |
2023-08-13 |
mouse |
| Cherl NamKoong, Min Sun Kim, Byeong-Tak Jang, Young Hee Lee, Young-Min Cho, Hyung Jin Cho. Central administration of GLP-1 and GIP decreases feeding in mice. Biochemical and biophysical research communications. vol 490. issue 2. 2017-09-26. PMID:28610922. |
the effect of glp-1 with gip on food intake, body weight, locomotor activity were determined following intracerebroventricular (icv) administration of glp-1 and/or gip in mice. |
2017-09-26 |
2023-08-13 |
mouse |
| Cherl NamKoong, Min Sun Kim, Byeong-Tak Jang, Young Hee Lee, Young-Min Cho, Hyung Jin Cho. Central administration of GLP-1 and GIP decreases feeding in mice. Biochemical and biophysical research communications. vol 490. issue 2. 2017-09-26. PMID:28610922. |
icv administration of low dose glp-1 (0.3 nmol) and gip (1 and 3 nmol) did not change food intake. |
2017-09-26 |
2023-08-13 |
mouse |
| Cherl NamKoong, Min Sun Kim, Byeong-Tak Jang, Young Hee Lee, Young-Min Cho, Hyung Jin Cho. Central administration of GLP-1 and GIP decreases feeding in mice. Biochemical and biophysical research communications. vol 490. issue 2. 2017-09-26. PMID:28610922. |
however, icv administration of higher doses glp-1 (1 and 3 nmol) and gip (6 nmol) significantly decreased food intake and body weight. |
2017-09-26 |
2023-08-13 |
mouse |
| Cherl NamKoong, Min Sun Kim, Byeong-Tak Jang, Young Hee Lee, Young-Min Cho, Hyung Jin Cho. Central administration of GLP-1 and GIP decreases feeding in mice. Biochemical and biophysical research communications. vol 490. issue 2. 2017-09-26. PMID:28610922. |
icv co-administration of glp-1 and gip significantly decreased food intake, body weight and drinking. |
2017-09-26 |
2023-08-13 |
mouse |
| Christine M Martin, Vadivel Parthsarathy, Annie Hasib, Ming T Ng, Stephen McClean, Peter R Flatt, Victor A Gault, Nigel Irwi. Biological Activity and Antidiabetic Potential of C-Terminal Octapeptide Fragments of the Gut-Derived Hormone Xenin. PloS one. vol 11. issue 3. 2016-08-22. PMID:27032106. |
xenin is a peptide that is co-secreted with the incretin hormone, glucose-dependent insulinotropic polypeptide (gip), from intestinal k-cells in response to feeding. |
2016-08-22 |
2023-08-13 |
mouse |
| Jiaqiang Zhou, Zheng Hao, Nigel Irwin, Hans-Rudolf Berthoud, Jianping Y. Gastric inhibitory polypeptide (GIP) is selectively decreased in the roux-limb of dietary obese mice after RYGB surgery. PloS one. vol 10. issue 8. 2016-05-17. PMID:26266950. |
serum gip (total) was significantly higher in the fasting condition, but not in the fed condition due to attenuated gip response to food intake in rygb mice. |
2016-05-17 |
2023-08-13 |
mouse |
| Jiaqiang Zhou, Zheng Hao, Nigel Irwin, Hans-Rudolf Berthoud, Jianping Y. Gastric inhibitory polypeptide (GIP) is selectively decreased in the roux-limb of dietary obese mice after RYGB surgery. PloS one. vol 10. issue 8. 2016-05-17. PMID:26266950. |
the loss of food-induced gip response in roux-limb of intestine likely contributes to the attenuated serum gip response to feeding. |
2016-05-17 |
2023-08-13 |
mouse |
| Fei Wang, Stephanie M Yoder, Qing Yang, Alison B Kohan, Tammy L Kindel, Jacob Wang, Patrick Ts. Chronic high-fat feeding increases GIP and GLP-1 secretion without altering body weight. American journal of physiology. Gastrointestinal and liver physiology. vol 309. issue 10. 2016-02-25. PMID:26336929. |
chronic high-fat feeding increases gip and glp-1 secretion without altering body weight. |
2016-02-25 |
2023-08-13 |
rat |
| Fei Wang, Stephanie M Yoder, Qing Yang, Alison B Kohan, Tammy L Kindel, Jacob Wang, Patrick Ts. Chronic high-fat feeding increases GIP and GLP-1 secretion without altering body weight. American journal of physiology. Gastrointestinal and liver physiology. vol 309. issue 10. 2016-02-25. PMID:26336929. |
the incretin hormones, glucose-dependent insulinotropic polypeptide (gip) and glucagon-like peptide-1 (glp-1), enhance postprandial insulin secretion, promote adipogenesis, and regulate gastrointestinal motility and food intake. |
2016-02-25 |
2023-08-13 |
rat |
| Ramona Pais, Fiona M Gribble, Frank Reiman. Stimulation of incretin secreting cells. Therapeutic advances in endocrinology and metabolism. vol 7. issue 1. 2016-02-17. PMID:26885360. |
the incretin hormones glucose-dependent insulinotropic polypeptide (gip) and glucagon like peptide-1 (glp-1) are secreted from enteroendocrine cells in the gut and regulate physiological and homeostatic functions related to glucose control, metabolism and food intake. |
2016-02-17 |
2023-08-13 |
Not clear |
| Sho-ichi Yamagishi, Kei Fukami, Takanori Matsu. Crosstalk between advanced glycation end products (AGEs)-receptor RAGE axis and dipeptidyl peptidase-4-incretin system in diabetic vascular complications. Cardiovascular diabetology. vol 14. 2016-01-15. PMID:25582643. |
glucagon-like peptide-1 (glp-1) and glucose-dependent insulinotropic polypeptide (gip) are incretins, gut hormones secreted from the intestine in response to food intake, both of which augment glucose-induced insulin release, suppress glucagon secretion, and slow gastric emptying. |
2016-01-15 |
2023-08-13 |
Not clear |
| R Charlotte Moffett, Srividya Vasu, Peter R Flat. Functional GIP receptors play a major role in islet compensatory response to high fat feeding in mice. Biochimica et biophysica acta. vol 1850. issue 6. 2015-08-31. PMID:25688757. |
functional gip receptors play a major role in islet compensatory response to high fat feeding in mice. |
2015-08-31 |
2023-08-13 |
mouse |
| Francisca Araujo, Neha Shrestha, Pedro L Granja, Jouni Hirvonen, Hélder A Santos, Bruno Sarment. Antihyperglycemic potential of incretins orally delivered via nano and microsystems and subsequent glucoregulatory effects. Current pharmaceutical biotechnology. vol 15. issue 7. 2015-05-26. PMID:25219868. |
the incretin based therapies mainly include incretin hormones which are glucose-dependent insulinotropic peptides (gip) and glucagon like peptide-1 (glp-1) released from the endocrinal cells in the small intestine in response to food intake. |
2015-05-26 |
2023-08-13 |
Not clear |