Gut hormone secretion in a new meal tolerance test on insulin, glucagon, and glycemic excursions in patients with morbid obesity undergone sleeve gastrectomy.

IF 3.1 2区 医学 Q1 ENDOCRINOLOGY & METABOLISM
Yukako Yamamoto, Masaki Kobayashi, Takeshi Togawa, Osamu Sekine, Yuki Ozamoto, Junko Fuse, Jun Ito-Kobayashi, Yasumitsu Oe, Akeo Hagiwara, Masanori Iwanishi, Akira Shimatsu, Tadahiro Kitamura, Atsunori Kashiwagi
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引用次数: 0

Abstract

We have reported that hypoglycemia during a 75-g oral glucose tolerance test (OGTT) in patients who underwent a laparoscopic sleeve gastrectomy (LSG) is prevented by a new mixed meal tolerance test (MTT) containing lipid, protein, and carbohydrate equivalent to 75-g glucose. We investigated whether the secretions of gut hormones, including glucagon-like peptide 1 (GLP-1), glucose-dependent insulinotropic polypeptide (GIP), and glicentin during OGTT, were involved in reactive hypoglycemia observed in post-LSG patients through changes in plasma insulin and glucagon secretions. Thus, we compared these gut hormone secretions during the OGTT and MTT in 30 Japanese patients pre- and 1-yr post-LSG. Both GLP-1 and glicentin secretions were glucose-dependently stimulated in pre-LSG patients and were enhanced by the LSG. This enhancement was associated with postprandial hypoglycemia through both enhanced acute insulin secretion and suppressed glucagon secretion during the OGTT in the post-LSG patients whose calculated disposition index improved. Conversely, the MTT in the post-LSG patients attenuated the insulin secretion and enhanced both GIP and glucagon secretions, resulting in protection of hypoglycemia. The GIP secretion was stimulated during the OGTT without association with insulin secretion, and the baseline GIP levels were positively correlated with HOMA-R in both pre- and post-LSG patients. In conclusion, the glucose-induced glicentin and GLP-1 secretions were associated with glucose-induced postprandial hypoglycemia through an overstimulation of acute insulin secretion in post-LSG patients. The new MTT is useful to evaluate normalization of glucose tolerance through attenuation of glucose-stimulated glicentin and GLP-1 secretions and enhanced GIP and glucagon secretions in post-LSG patients.NEW & NOTEWORTHY In postlaparoscopic sleeve gastrectomy (LSG) patients with enhanced disposition index, the standard OGTT resulted in postprandial reactive hypoglycemia, precluding accurate assessment of glucose tolerance. Glucose-induced glicentin and GLP-1 secretions were implicated in this phenomenon. However, a mixed meal test using 75-g carbohydrate, fat, and protein attenuated such reactive hypoglycemia, providing an accurate assessment of glucose tolerance through attenuation of both glicentin and GLP-1 oversecretions and enhanced GIP and glucagon secretions in post-LSG patients.

一项新的膳食耐量试验对实施袖胃切除术的病态肥胖患者胰岛素、胰高血糖素和血糖升高的影响。
我们曾报道,在接受腹腔镜袖胃切除术(LSG)的患者进行75克口服葡萄糖耐量试验(OGTT)期间,通过一种新的混合膳食耐量试验(MTT)预防低血糖,该试验含有相当于75克葡萄糖的脂质、蛋白质和碳水化合物。我们研究了胰高血糖素样肽1 (GLP-1)、葡萄糖依赖性胰岛素性多肽(GIP)和胰高血糖素等肠道激素的分泌是否参与了lsg后患者血浆胰岛素和胰高血糖素分泌的变化。因此,我们比较了30名日本患者在lsg术前和术后1年的OGTT和MTT期间的肠道激素分泌。LSG前患者GLP-1和glicentin的分泌均受到葡萄糖依赖性刺激,并因LSG而增强。这种增强与餐后低血糖有关,在OGTT期间,lsg后患者的急性胰岛素分泌增强,胰高血糖素分泌抑制,其计算的处置指数改善。相反,lsg后患者的MTT降低了胰岛素分泌和f分泌,基线GIP水平与Tg分泌的HOMA-R呈正相关,基线GIP水平与lsg前和lsg后患者的HOMA-R呈正相关。综上所述,葡萄糖诱导的glicentin和GLP-1分泌与葡萄糖诱导的餐后低血糖有关,其机制是通过过度刺激lsg后患者的急性胰岛素分泌。新的MTT可通过葡萄糖刺激的glicentin和GLP-1分泌的衰减以及lsg后患者GIP和胰高血糖素分泌的增强来评估葡萄糖耐量的正常化。
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来源期刊
CiteScore
9.80
自引率
0.00%
发文量
98
审稿时长
1 months
期刊介绍: The American Journal of Physiology-Endocrinology and Metabolism publishes original, mechanistic studies on the physiology of endocrine and metabolic systems. Physiological, cellular, and molecular studies in whole animals or humans will be considered. Specific themes include, but are not limited to, mechanisms of hormone and growth factor action; hormonal and nutritional regulation of metabolism, inflammation, microbiome and energy balance; integrative organ cross talk; paracrine and autocrine control of endocrine cells; function and activation of hormone receptors; endocrine or metabolic control of channels, transporters, and membrane function; temporal analysis of hormone secretion and metabolism; and mathematical/kinetic modeling of metabolism. Novel molecular, immunological, or biophysical studies of hormone action are also welcome.
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