Repetitive transcranial magnetic stimulation in the treatment of resistant depression: changes of specific neurotransmitter precursor amino acids.
Phenylalanine
Phenylalanine hydroxylase
Transcranial magnetic stimulation
Treatment-resistant depression
Tyrosine
Journal
Journal of neural transmission (Vienna, Austria : 1996)
ISSN: 1435-1463
Titre abrégé: J Neural Transm (Vienna)
Pays: Austria
ID NLM: 9702341
Informations de publication
Date de publication:
08 2021
08 2021
Historique:
received:
10
02
2021
accepted:
02
06
2021
pubmed:
11
7
2021
medline:
28
10
2021
entrez:
10
7
2021
Statut:
ppublish
Résumé
Repetitive transcranial magnetic stimulation (rTMS) for treatment-resistant major depression offers an alternative therapy, since more than every third patient is not responding to adequate antidepressive treatment. In this interventional study safety, symptom development and changes of serum concentrations of neurotransmitter precursor amino acids, of immune activation and inflammation markers, of brain-derived neurotrophic factor (BDNF), nitrite as well as of salivary amylase were measured before and after a frontal polar cortex stimulation using rTMS as add-on treatment in 38 patients with treatment-resistant depression. Out of these, 17 patients received sham stimulation as a control. Treatment was well tolerated: with the exception of one patient of the verum group, who described discomfort during the second treatment, no serious adverse effects were observed. Improvement of depression with a significant decrease in the HAMD-7 scale (p = 0.001) was found in patients treated with rTMS, but not in sham-treated patients. Furthermore, serum phenylalanine and tyrosine dropped significantly (p = 0.03 and p = 0.027, respectively) in rTMS-treated patients. The kynurenine to tryptophan ratio (Kyn/Trp) tended to decrease under rTMS (p = 0.07). In addition, associations between concentrations of BDNF and neopterin as well as serum nitrite levels were found in patients after rTMS treatment, which indicates an influence of immune regulatory circuits on BDNF levels. In the sham-treated patients, no changes of biomarker concentrations were observed. Results show that rTMS is effective in the treatment of resistant depression. rTMS appears to influence the enzyme phenylalanine hydroxylase, which plays a central role in the biosynthesis of neurotransmitter precursors tyrosine and dihydroxyphenylalanine (DOPA).
Identifiants
pubmed: 34244826
doi: 10.1007/s00702-021-02363-7
pii: 10.1007/s00702-021-02363-7
pmc: PMC8321996
doi:
Substances chimiques
Amino Acids
0
Neurotransmitter Agents
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
1225-1231Informations de copyright
© 2021. The Author(s).
Références
Curr Drug Metab. 2008 Sep;9(7):622-7
pubmed: 18781914
Acta Psychiatr Scand. 1994 Jul;90(1):10-3
pubmed: 7976441
Psychoneuroendocrinology. 2017 Feb;76:197-205
pubmed: 27960139
Clin Biochem. 2013 Dec;46(18):1848-51
pubmed: 24183885
J Neural Transm (Vienna). 2019 Aug;126(8):1105-1110
pubmed: 31250285
Neuroreport. 2015 Dec 16;26(18):1145-50
pubmed: 26512932
Neuron. 2007 Jul 19;55(2):187-99
pubmed: 17640522
Brain Stimul. 2015 Mar-Apr;8(2):208-15
pubmed: 25465290
Front Psychiatry. 2020 Feb 26;11:71
pubmed: 32174850
Trends Cogn Sci. 2017 May;21(5):357-371
pubmed: 28363681
Brain Commun. 2020 Nov 16;2(2):fcaa196
pubmed: 33364600
Clin Chem. 1997 Dec;43(12):2424-6
pubmed: 9439467
Hum Brain Mapp. 2019 Oct 15;40(15):4301-4315
pubmed: 31268615
J Neurosci Methods. 2011 Oct 15;201(2):327-32
pubmed: 21871491
Prog Neuropsychopharmacol Biol Psychiatry. 2019 Jan 10;88:31-40
pubmed: 29953934
J Clin Psychiatry. 2011 May;72(5):e18
pubmed: 21658343
Biol Psychiatry. 2011 Jul 15;70(2):175-82
pubmed: 21277567
Psychol Med. 2015 Dec;45(16):3411-32
pubmed: 26349810
Brain Stimul. 2019 Mar - Apr;12(2):364-366
pubmed: 30448078
Neuroimage Clin. 2019;23:101877
pubmed: 31170685
J Neural Transm (Vienna). 2000;107(3):343-53
pubmed: 10821443
Brain Behav Immun. 2002 Oct;16(5):501-2
pubmed: 12401463
Curr Alzheimer Res. 2018;15(12):1106-1113
pubmed: 30101706
Br J Psychiatry. 2009 Sep;195(3):211-7
pubmed: 19721109
Neuroreport. 2020 Jun 7;31(9):629-636
pubmed: 32427708
BMC Psychiatry. 2014 Nov 30;14:342
pubmed: 25433539
Lancet. 2018 Apr 28;391(10131):1683-1692
pubmed: 29726344
Front Hum Neurosci. 2017 Nov 06;11:526
pubmed: 29163106
J Clin Psychiatry. 2012 Apr;73(4):e567-73
pubmed: 22579164
Prog Neuropsychopharmacol Biol Psychiatry. 2014 Jan 3;48:268-76
pubmed: 23085509
Biol Psychiatry. 2003 Apr 15;53(8):649-59
pubmed: 12706951
Curr Neuropharmacol. 2018;16(5):533-558
pubmed: 29173175
Nat Neurosci. 2015 Oct;18(10):1386-93
pubmed: 26404713
J Clin Exp Neuropsychol. 2001 Aug;23(4):424-30
pubmed: 11780943
CMAJ. 2005 Nov 22;173(11):1327-34
pubmed: 16301700
J Int Med Res. 2019 May;47(5):1848-1855
pubmed: 30616482
JAMA. 2017 Apr 18;317(15):1517
pubmed: 28418490
Pharmacol Ther. 2020 Apr;208:107494
pubmed: 31991195
Neuron. 2019 Apr 3;102(1):75-90
pubmed: 30946828
J Exp Med. 1983 Sep 1;158(3):670-89
pubmed: 6411853
Brain Behav Immun. 2002 Oct;16(5):590-5
pubmed: 12401473
Biol Psychiatry. 2003 Aug 1;54(3):208-15
pubmed: 12893097
PLoS One. 2016 Mar 23;11(3):e0152241
pubmed: 27007747