ANTIDEPRESSANT THERAPY AND HYPOGLYCEMIA
抗抑郁治疗和低血糖
基本信息
- 批准号:7140214
- 负责人:
- 金额:$ 13.37万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2005
- 资助国家:美国
- 起止时间:2005-08-01 至 2007-07-31
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
DESCRIPTION (provided by applicant): Findings from the Diabetes Control and Complications Trial have shown that tight glycemic control, achieved through intensive insulin therapy, prevents and reduces the onset and progression of the complications associated with uncontrolled diabetes. To achieve this, a high level of patient self-care is critical. Patients with diabetes, however, are twice as likely to develop depression compared to the general population. For diabetic patients with co-morbid depression, diligent self-care and diabetes management can be profoundly impaired, resulting in a significantly greater risk of developing diabetes-related complications and morbidity. The commonly prescribed antidepressant class of selective serotonin reuptake inhibitors (SSRIs) has been associated with significant incidence of hypoglycemia. The mechanism(s) underlying this have not been elucidated. The proposed studies will test the hypothesis that the SSRIs may impair the ability of the brain to detect hypoglycemia by reducing the responsiveness of hindbrain glucose sensing neurons that are critical to hypoglycemia detection and activation of counterregulatory responses. The following hypotheses will be tested: I) Peripheral administration of SSRIs decrease the counterregulatory response to hypoglycemia and II) SSRIs delivered directly into the terminal fields of hindbrain glucose sensing neurons impair the counterregulatory response to hypoglycemia. To test these hypotheses we will administer sertraline, acutely or chronically, to non-diabetic Wistar rats and will measure the neuroendocrine counterregulatory response to a bout of hypoglycemia. Finally, patients with diabetes exhibit a significant increase in severe hypoglycemic episodes. Thus, we will test the hypothesis III) that SSRIs are more detrimental to counterregulation in diabetic vs. non-diabetic rats. The results of these studies will provide new knowledge that ultimately may assist primary physicians in determining the most advantageous treatment for their diabetic patients with depression.
描述(由申请人提供):糖尿病控制和并发症试验的结果表明,通过强化胰岛素治疗实现的严格血糖控制可预防和减少与未控制的糖尿病相关的并发症的发生和进展。要做到这一点,高水平的患者自我护理至关重要。然而,糖尿病患者患抑郁症的可能性是普通人群的两倍。对于患有共病抑郁症的糖尿病患者,勤奋的自我护理和糖尿病管理可能会严重受损,导致发生糖尿病相关并发症和发病率的风险显著增加。常用的抗抑郁药选择性5-羟色胺再摄取抑制剂(SSRIs)与低血糖的发生率显著相关。其机制尚未阐明。拟定的研究将检验SSRI可能通过降低后脑葡萄糖感知神经元的反应性(对低血糖检测和反调节反应的激活至关重要)来损害大脑检测低血糖的能力的假设。将检验以下假设:I)SSRI外周给药降低对低血糖的反调节反应,II)直接递送至后脑葡萄糖感应神经元终末区域的SSRI损害对低血糖的反调节反应。为了检验这些假设,我们将舍曲林,急性或慢性,非糖尿病Wistar大鼠,并将测量神经内分泌反调节反应,一轮低血糖。最后,糖尿病患者严重低血糖发作显著增加。因此,我们将检验假设III),即SSRIs对糖尿病大鼠的反调节作用比非糖尿病大鼠更有害。这些研究的结果将提供新的知识,最终可能有助于初级医生确定最有利的治疗糖尿病患者抑郁症。
项目成果
期刊论文数量(0)
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科研奖励数量(0)
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DIANNE FIGLEWICZ LATTEMANN其他文献
DIANNE FIGLEWICZ LATTEMANN的其他文献
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{{ truncateString('DIANNE FIGLEWICZ LATTEMANN', 18)}}的其他基金
Dietary fatty acids, cell signals, and sucrose intake
膳食脂肪酸、细胞信号和蔗糖摄入量
- 批准号:
10046298 - 财政年份:2018
- 资助金额:
$ 13.37万 - 项目类别:
CNS Mechanisms of Acute Hypoglycemia-Associate Autonomic Failure
急性低血糖相关自主神经衰竭的中枢神经系统机制
- 批准号:
8258198 - 财政年份:2009
- 资助金额:
$ 13.37万 - 项目类别:
CNS Mechanisms of Acute Hypoglycemia-Associate Autonomic Failure
急性低血糖相关自主神经衰竭的中枢神经系统机制
- 批准号:
7782818 - 财政年份:2009
- 资助金额:
$ 13.37万 - 项目类别:
CNS Mechanisms of Acute Hypoglycemia-Associate Autonomic Failure
急性低血糖相关自主神经衰竭的中枢神经系统机制
- 批准号:
7686674 - 财政年份:2009
- 资助金额:
$ 13.37万 - 项目类别:
CNS Mechanisms of Acute Hypoglycemia-Associate Autonomic Failure
急性低血糖相关自主神经衰竭的中枢神经系统机制
- 批准号:
8195898 - 财政年份:2009
- 资助金额:
$ 13.37万 - 项目类别:
CNS Stress Pathways and the Development of Acute HAAF
CNS 应激通路与急性 HAAF 的发展
- 批准号:
6645366 - 财政年份:2002
- 资助金额:
$ 13.37万 - 项目类别:
CNS Stress Pathways and the Development of Acute HAAF
CNS 应激通路与急性 HAAF 的发展
- 批准号:
6548808 - 财政年份:2002
- 资助金额:
$ 13.37万 - 项目类别:
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