Desipramine Induces Cardiac Beta-Adrenergic Sensitivity Decrease in Major Depressed Patients without Relationship to Therapeutic Response

1990 ◽  
Vol 23 (06) ◽  
pp. 283-286 ◽  
Author(s):  
G. Bertschy ◽  
S. Vandel ◽  
A. Puech ◽  
D. Blum ◽  
B. Vandel ◽  
...  
2011 ◽  
Vol 134 (1-3) ◽  
pp. 421-426 ◽  
Author(s):  
Jianhua Shen ◽  
Naheed Hossain ◽  
David L. Streiner ◽  
Aruu V. Ravindran ◽  
Xuehua Wang ◽  
...  

1988 ◽  
Vol 152 (5) ◽  
pp. 665-669 ◽  
Author(s):  
Richard P. Ebstein ◽  
Bernard Lerer ◽  
Baruch Shapira ◽  
Zecharia Shemesh ◽  
Daniel G. Moscovich ◽  
...  

Beta-adrenergic-mediated cyclic AMP accumulation was reduced in lymphocytes obtained from depressed patients from that observed in an age- and sex-matched group of control subjects. Among the depressed patients, those not responding to treatment showed significantly lower pretreatment responses to isoproterenol compared with patients who exhibited significant clinical improvement during antidepressant treatment. Late-night (terminal) insomnia was significantly associated with the blunted response to beta-adrenergic stimulation. In depressed patients with the lowest isoproterenol response, the effect of forskolin (which acts distal to the receptor and directly stimulates the catalytic subunit) on cyclic AMP accumulation was also significantly decreased. This suggests that post-receptor modulations of signal amplification also play a role in the reduced response to beta-adrenergic stimulation in depression.


2018 ◽  
Vol 24 ◽  
pp. 3136-3145 ◽  
Author(s):  
Zuzana Vancova ◽  
Martina Cizmarikova ◽  
Jozef Dragasek ◽  
Silvia Zofcakova ◽  
Peter Kolarcik ◽  
...  

1989 ◽  
Vol 25 (7) ◽  
pp. A206-A207 ◽  
Author(s):  
Andrew Winokur ◽  
Jay D. Amsterdam ◽  
Neil Berwish ◽  
Jennifer L. Phillips ◽  
Greg Maislin

2013 ◽  
Vol 2013 ◽  
pp. 1-3
Author(s):  
Shahzad M. Alikhan ◽  
Jessica A. Lee ◽  
Luiz Dratcu

Depression has been shown to be associated with systemic inflammatory activity and the mode of action of several antidepressants appears to involve immunomodulation. Effects on immune system activity have also recently been observed in correlation with therapeutic response to mirtazapine in cardiac patients with depression, but no study has yet examined these effects in otherwise physically healthy depressed patients treated with mirtazapine. This report describes an association between a clinical antidepressant response and a decrease in markers of systemic inflammation observed during pharmacotherapy with mirtazapine in a severely depressed but physically well patient. This observation adds to the evidence that changes in inflammatory responses may be implicated in the mode of action of antidepressants. Further studies of antidepressant responses to mirtazapine and levels of inflammatory markers in depressed patients without medical comorbidity can help elucidate the role of the immune system in the pathophysiology of depression, and hence contribute to the development of novel antidepressant therapies.


2013 ◽  
Vol 6 (7) ◽  
pp. e201303003 ◽  
Author(s):  
Liana E. Kafetzopoulou ◽  
David J. Boocock ◽  
Gopal Krishna R. Dhondalay ◽  
Desmond G. Powe ◽  
Graham R. Ball

1987 ◽  
Vol 22 (4) ◽  
pp. 265-273 ◽  
Author(s):  
Ghanshyam N. Pandey ◽  
Philip G. Janicak ◽  
John M. Davis

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