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联合腹腔和肝迷走神经神经调节可逆转葡萄糖不耐受并改善前驱和显性2型糖尿病患者的血糖控制。

Combining Celiac and Hepatic Vagus Nerve Neuromodulation Reverses Glucose Intolerance and Improves Glycemic Control in Pre- and Overt-Type 2 Diabetes Mellitus.

作者信息

Waataja Jonathan J, Asp Anders J, Billington Charles J

机构信息

ReShape Lifesciences Inc., Irvine, CA 92618, USA.

Department of Physical Medicine and Rehabilitation, Mayo Clinic, Rochester, MN 55605, USA.

出版信息

Biomedicines. 2023 Sep 4;11(9):2452. doi: 10.3390/biomedicines11092452.

DOI:10.3390/biomedicines11092452
PMID:37760895
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10525327/
Abstract

Neurological disorders and type 2 diabetes mellitus (T2DM) are deeply intertwined. For example, autonomic neuropathy contributes to the development of T2DM and continued unmanaged T2DM causes further progression of nerve damage. Increasing glycemic control has been shown to prevent the onset and progression of diabetic autonomic neuropathies. Neuromodulation consisting of combined stimulation of celiac vagal fibers innervating the pancreas with concurrent electrical blockade of neuronal hepatic vagal fibers innervating the liver has been shown to increase glycemic control in animal models of T2DM. The present study demonstrated that the neuromodulation reversed glucose intolerance in alloxan-treated swine in both pre- and overt stages of T2DM. This was demonstrated by improved performance on oral glucose tolerance tests (OGTTs), as assessed by area under the curve (AUC). In prediabetic swine (fasting plasma glucose (FPG) range: 101-119 mg/dL) the median AUC decreased from 31.9 AUs (IQR = 28.6, 35.5) to 15.9 AUs (IQR = 15.1, 18.3) = 0.004. In diabetic swine (FPG range: 133-207 mg/dL) the median AUC decreased from 54.2 AUs (IQR = 41.5, 56.6) to 16.0 AUs (IQR = 15.4, 21.5) = 0.003. This neuromodulation technique may offer a new treatment for T2DM and reverse glycemic dysregulation at multiple states of T2DM involved in diabetic neuropathy including at its development and during progression.

摘要

神经系统疾病与2型糖尿病(T2DM)紧密相连。例如,自主神经病变会促使T2DM的发展,而T2DM若持续未得到有效控制会导致神经损伤进一步恶化。研究表明,加强血糖控制可预防糖尿病自主神经病变的发生与发展。在T2DM动物模型中,对支配胰腺的腹腔迷走神经纤维进行联合刺激并同时对支配肝脏的肝迷走神经纤维进行电阻滞的神经调节,已被证明可改善血糖控制。本研究表明,这种神经调节可逆转四氧嘧啶处理的猪在T2DM前期和显性期的葡萄糖不耐受情况。这通过口服葡萄糖耐量试验(OGTT)表现的改善得到证明,采用曲线下面积(AUC)进行评估。在糖尿病前期猪(空腹血糖(FPG)范围:101 - 119 mg/dL)中,AUC中位数从31.9 AU(四分位间距 = 28.6,35.5)降至15.9 AU(四分位间距 = 15.1,18.3),P = 0.004。在糖尿病猪(FPG范围:133 - 207 mg/dL)中,AUC中位数从54.2 AU(四分位间距 = 41.5,56.6)降至16.0 AU(四分位间距 = 15.4,21.5),P = 0.003。这种神经调节技术可能为T2DM提供一种新的治疗方法,并在T2DM涉及糖尿病神经病变的多个阶段,包括其发展阶段和进展过程中,逆转血糖失调。

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