实验性药理方法来逆转低血糖症意识的受损-一篇评论
Hiba Z Hashmi1, Ameer Khowaja2, Amir Moheet1
1Division of Diabetes, Endocrinology and Metabolism, Department of Medicine, University of Minnesota, Minneapolis, MN, United States.
Frontiers in pharmacology
|February 7, 2024
概括
糖尿病患者对低血糖症 (IAH) 的意识受损是由于对抗调节反应减少的结果. 本综述审查了用于预防和治疗IAH的药物干预措施,这对于管理糖尿病并发症至关重要.
科学领域:
- 内分泌学 在内分泌学.
- 神经科学是一个神经科学.
- 药理学 药理学是指药理学的学科.
背景情况:
- 糖尿病管理的负担是低血糖,一个危险的并发症.
- 生理学反调节反应可以防止低血糖症,但随着时间的推移可能会减弱.
- 复发性低血糖症可能导致低血糖症 (IAH) 的意识受损,增加严重发作风险.
研究的目的:
- 审查药物干预措施的有效性和可行性,以预防和治疗IAH.
- 探索复杂的疾病的潜在治疗策略,以各种各样的致病机制.
主要方法:
- 临床和临床前研究的全面审查.
- 对针对IAH机制的药物剂的检查.
主要成果:
- 讨论的药物包括N-乙囊,GABA A受体抑制剂,阿片类受体对抗剂等.
- 分析了各种药物干预措施的有效性和可行性数据.
结论:
- 由于其复杂性,IAH在糖尿病护理中提出了重大挑战.
- 药物干预为管理和预防IAH提供了潜在的战略,尽管需要进一步的研究.
相关概念视频
Hypoglycemia and Glucagon
263
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...
263
Oral Hypoglycemic Agents: Biguanides and Glitazones
204
Biguanides, particularly metformin (Glucophage), are insulin sensitizers that enhance glucose uptake, thereby reducing insulin resistance. Unlike sulfonylureas, metformin doesn't prompt insulin secretion, which helps to curb hypoglycemia risk. Metformin is beneficial in treating conditions like polycystic ovary syndrome due to its insulin-resistance reduction capability. The drug's primary action involves curtailing hepatic gluconeogenesis, a significant contributor to high blood...
204
Glucagon-like Receptor Agonists
323
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...
323
Oral Hypoglycemic Agents: Glinides
154
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...
154


