The effect of antidepressants on glucose homeostasis and insulin sensitivity: synthesis and mechanisms

被引:155
作者
McIntyre, RS
Soczynska, JK
Konarski, JZ
Kennedy, SH
机构
[1] Univ Toronto, Dept Psychiat, Univ Hlth Network, Toronto, ON M5T 2S8, Canada
[2] Univ Toronto, Inst Med Sci, Toronto, ON M5S 1A1, Canada
[3] Univ Hlth Network, Mood Disorders Psychopharmacol Unit, Toronto, ON, Canada
关键词
antidepressant; depression; diabetes; glucose homeostasis; insulin sensitivity;
D O I
10.1517/14740338.5.1.157
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Objective: To synthesise results from investigations reporting on the effect of antidepressants on glucose-insulin homeostasis. Method: The authors conducted a MedLine search of all English language articles from 1966 to October 2005 using the keywords: bipolar disorder, major depressive disorder, diabetes mellitus, glucose homeostasis, and the name of each antidepressant that has been indicated for major depression in Canada and the US up to October 2005. The search was supplemented with a manual review of relevant references. Both preclinical and clinical investigations were reviewed. Results: Some serotonergic antidepressants (e.g., fluoxetine) reduce hyperglycaemia, normalise glucose homeostasis and increase insulin sensitivity, whereas some noradrenergic antidepressants (e.g., desipramine) exert opposite effects. Dual-mechanism antidepressants (e.g., duloxetine and venlafaxine) do not appear to disrupt glucose homeostatic dynamics, whereas nonselective hydrazine monoamine oxidase inhibitors (e.g., phenelzine) are associated with hypoglycaemia and an increased glucose disposal rate. Conclusion: Some antidepressants exert a clinically significant effect on metabolism relevant to both therapeutic outcome and adverse events.
引用
收藏
页码:157 / 168
页数:12
相关论文
共 75 条
[1]  
ASBERG M, 1976, SCIENCE, V191, P478
[2]   High numbers of circulating activated T cells and raised levels of serum IL-2 receptor in bipolar disorder [J].
Breunis, MN ;
Kupka, RW ;
Nolen, WA ;
Suppes, T ;
Denicoff, KD ;
Leverich, GS ;
Post, RM ;
Drexhage, HA .
BIOLOGICAL PSYCHIATRY, 2003, 53 (02) :157-165
[3]   Association of depression with medical illness: Does cortisol play a role? [J].
Brown, ES ;
Varghese, FP ;
McEwen, BS .
BIOLOGICAL PSYCHIATRY, 2004, 55 (01) :1-9
[4]   DURATION OF STREPTOZOTOCIN DIABETES INFLUENCES THE RESPONSE OF HYPOTHALAMIC SEROTONIN METABOLISM TO IMMOBILIZATION STRESS [J].
CHAOULOFF, F ;
LAUDE, D ;
MERINO, D ;
SERRURIER, B ;
BAUDRIE, V ;
ELGHOZI, JL .
NEUROENDOCRINOLOGY, 1989, 50 (03) :344-350
[5]   Insulin and neurodegenerative disease: shared and specific mechanisms [J].
Craft, S ;
Watson, GS .
LANCET NEUROLOGY, 2004, 3 (03) :169-178
[6]   REDUCTION IN BRAIN-SEROTONIN SYNTHESIS RATE IN STREPTOZOTOCIN-DIABETIC RATS [J].
CRANDALL, EA ;
GILLIS, MA ;
FERNSTROM, JD .
ENDOCRINOLOGY, 1981, 109 (01) :310-312
[7]   Cytokine-induced sickness behaviour: a neuroimmune response to activation of innate immunity [J].
Dantzer, R .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2004, 500 (1-3) :399-411
[8]   Prevalence, severity, and unmet need for treatment of mental disorders in the World Health Organization World Mental Health Surveys [J].
Demyttenaere, K ;
Bruffaerts, R ;
Posada-Villa, J ;
Gasquet, I ;
Kovess, V ;
Lepine, JP ;
Angermeyer, MC ;
Bernert, S ;
de Girolamo, G ;
Morosini, P ;
Polidori, G ;
Kikkawa, T ;
Kawakami, N ;
Ono, Y ;
Takeshima, T ;
Uda, H ;
Karam, EG ;
Fayyad, JA ;
Karam, AN ;
Mneimneh, ZN ;
Medina-Mora, ME ;
Borges, G ;
Lara, C ;
de Graaf, R ;
Ormel, J ;
Gureje, O ;
Shen, YC ;
Huang, YQ ;
Zhang, MY ;
Alonso, J ;
Haro, JM ;
Vilagut, G ;
Bromet, EJ ;
Gluzman, S ;
Webb, C ;
Kessler, RC ;
Merikangas, KR ;
Anthony, JC ;
Von Korff, MR ;
Wang, PS ;
Alonso, J ;
Brugha, TS ;
Aguilar-Gaxiola, S ;
Lee, S ;
Heeringa, S ;
Pennell, BE ;
Zaslavsky, AM ;
Ustun, TB ;
Chatterji, S .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2004, 291 (21) :2581-2590
[9]   Inflammatory mediators and islet β-cell failure:: a link between type 1 and type 2 diabetes [J].
Donath, MY ;
Storling, J ;
Maedler, K ;
Mandrup-Poulsen, T .
JOURNAL OF MOLECULAR MEDICINE-JMM, 2003, 81 (08) :455-470
[10]   The serotonergic agent fluoxetine reduces neuropeptide Y levels and neuropeptide Y secretion in the hypothalamus of lean and obese rats [J].
Dryden, S ;
Frankish, HM ;
Wang, Q ;
Pickavance, L ;
Williams, G .
NEUROSCIENCE, 1996, 72 (02) :557-566