由肠道微生物群衍生而来的N-乙色氨介导的金赛诺化物化合物K的低血糖作用
Su-Tian-Zi Huang1,2, Yu-Hui Hu1, Yong-Chao Gao1
1Engineering Research Center of Applied Technology of Pharmacogenomics (Ministry of Education, China), Hunan Key Laboratory of Pharmacomicrobiomics, Department of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha, China.
Phytotherapy research : PTR
|January 6, 2025
概括
金色化物化合物K (GCK) 通过改变肠道微生物群来改善2型糖尿病,正如小鼠模型所示. 这种效应可以通过便微生物群移植进行转移,突出显示了GCK.
科学领域:
- 微生物学 微生物学
- 代谢过程中的代谢.
- 药理学 药理学是指药理学的学科.
背景情况:
- 金色化物化合物K (GCK) 呈现出与肠道微生物群相关的低血糖效应.
- 通过肠道微生物群,GCK通过高脂肪饮食 (HFD) 改善2型糖尿病 (T2D) 的确切机制尚不清楚.
研究的目的:
- 在HFD诱导的T2D小鼠模型中研究GCK的低血糖效应和潜在机制.
- 阐明肠道微生物群在介导 GCK 的治疗作用中的作用.
主要方法:
- 已建立的HFD诱导的伪无细菌 (GF) T2D小鼠模型.
- 利用便微生物群移植 (FMT) 实验来评估肠道微生物群的作用.
- 进行了非向代谢和ELISA分析,以分析类似葡萄糖-1 (GLP-1) 的分析.
主要成果:
- 在HFD诱导的糖尿病小鼠中,GCK治疗缓解了代谢障碍和调节了肠道微生物群.
- 通过FMT,GCK的低血糖效应可转移到伪GF糖尿病小鼠.
- GCK增加了N-乙血素 (NAS) 水平,而NAS的使用改善了HFD小鼠的胰岛素敏感性和GLP-1分泌.
结论:
- GCK通过改变肠道微生物群的组成和功能来产生低血糖作用.
- N-乙血素 (NAS) 是一种关键的代谢物,它调解了GCK对葡萄糖代谢和GLP-1分泌的有益作用.
相关概念视频
Drugs Affecting GI Tract Motility: Serotonin Receptor Agonists
170
Serotonin, a crucial neurotransmitter synthesized by enterochromaffin cells, plays a cardinal role in regulating gastrointestinal (GI) motility. With over 90% of the body's total serotonin in the GI tract, its influence on digestive processes is profound. Serotonin is swiftly released upon various stimuli, such as food boluses or certain drugs, triggering intrinsic sensory neurons in the myenteric plexus and extrinsic vagal and spinal sensory neurons. This leads to the activation of the...
170
Oral Hypoglycemic Agents: α-Glucosidase Inhibitors
104
α-glucosidase inhibitors, including acarbose (Precose), miglitol (Glyset), and voglibose (Voglib) (primarily available in Asia), are drugs that control blood sugar levels by delaying the digestion of starch and disaccharides. They achieve this by inhibiting α-glucosidase enzymes in the intestine, which slow the absorption of carbohydrates in the intestine, which in turn leads to a prolonged release of the glucoregulatory hormone GLP-1 from intestinal L-cells.
Acarbose and miglitol are...
Acarbose and miglitol are...
104
Glucagon-like Receptor Agonists
249
Incretins include glucagon-like peptide-1 (GLP-1) and glucose-dependent insulinotropic polypeptide (GIP), which stimulate insulin secretion post-meals. In type 2 diabetes, GIP's efficacy is reduced, making GLP-1 a viable drug target. GIP originates from preproGIP.
GLP-1, when administered in high doses intravenously, triggers insulin secretion, inhibits glucagon release, slows gastric emptying, reduces food intake, and restores normal insulin secretion. However, its rapid inactivation by...
GLP-1, when administered in high doses intravenously, triggers insulin secretion, inhibits glucagon release, slows gastric emptying, reduces food intake, and restores normal insulin secretion. However, its rapid inactivation by...
249
Oral Hypoglycemic Agents: Glinides
108
Repaglinide (Prandin) and Nateglinide (Starlix), known as glinides, are oral insulin secretagogues that stimulate insulin release from pancreatic β cells by closing the ATP-sensitive potassium channels (KATP channel). Repaglinide controls insulin release from pancreatic β cells by managing potassium efflux. It shares two binding sites with sulfonylureas and also has a unique site, indicating overlapping mechanisms of action. With a rapid onset and a 4-7 hour duration, it effectively...
108
Hypoglycemia and Glucagon
131
Without prolonged fasting, healthy individuals maintain blood glucose levels above 3.5 mM due to a well-adapted neuroendocrine counterregulatory system that effectively prevents acute hypoglycemia, a potentially life-threatening condition. The primary clinical scenarios for hypoglycemia encompass diabetes treatment, inappropriate production of endogenous insulin or insulin-like substances by tumors, and the use of glucose-lowering agents in non-diabetic individuals. Notably, hypoglycemia in the...
131
Dipeptidyl Peptidase 4 Inhibitors
117
Dipeptidyl peptidase 4 (DPP-4) is a serine protease widely distributed in the body. It's involved in the inactivation of GLP-1 and GIP hormones, which are crucial for insulin regulation. DPP-4 inhibitors, such as sitagliptin (Januvia), saxagliptin (Onglyza), linagliptin (Tradjenta), alogliptin (Nesina), and vildagliptin (Galvus), help increase the proportion of active GLP-1, enhancing insulin secretion. These inhibitors work by competitively binding to DPP-4. This binding causes a...
117


