Deep TMS on alcoholics: effects on cortisolemia and dopamine pathway modulation. A pilot study

被引:124
作者
Ceccanti, Marco [1 ]
Inghilleri, Maurizio [1 ]
Attilia, Maria Luisa [2 ]
Raccah, Ruggero [3 ]
Fiore, Marco [4 ]
Zangen, Abraham [5 ]
Ceccanti, Mauro [2 ]
机构
[1] Univ Roma La Sapienza, Dept Neurol & Psychiat, I-00161 Rome, Italy
[2] Univ Roma La Sapienza, Dept Clin Med, I-00161 Rome, Italy
[3] ATID, I-00198 Rome, Italy
[4] EBRI CNR, I-00143 Rome, Italy
[5] Ben Gurion Univ Negev, Dept Life Sci, IL-84105 Beer Sheva, Israel
关键词
alcohol; prefrontal cortex; transcranic magnetic stimulation; cortisol; prolactin; TRANSCRANIAL MAGNETIC STIMULATION; CORTICOTROPIN-RELEASING-FACTOR; MEDIAL PREFRONTAL CORTEX; ADRENAL AXIS ACTIVITY; DRUG-ADDICTION; ELECTRIC-FIELD; SUBSTANCE USE; STRESS; BRAIN; PITUITARY;
D O I
10.1139/cjpp-2014-0188
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
The hypothalamic pituitary adrenal axis and dopamine have a key role in transition from alcohol social use to addiction. The medial prefrontal cortex was shown to modulate dopaminergic activity and cortisol releasing factor (CRF) release in hypothalamic and extra-hypothalamic systems. The recent advancements in non-invasive neurostimulation technologies has enabled stimulation of deeper brain regions using H-coil transcranial magnetic stimulation (TMS) in humans. This randomized double-blind placebo-controlled pilot study aims to evaluate H-coil efficacy in stimulating the medial prefrontal cortex. Cortisolemia and prolactinemia were evaluated as effectiveness markers. Alcohol intake and craving were considered as secondary outcomes. Eighteen alcoholics were recruited and randomized into 2 homogeneous groups: 9 in the real stimulation group and 9 in the sham stimulation group. Repetitive TMS (rTMS) was administered through a magnetic stimulator over 10 sessions at 20 Hz, directed to the medial prefrontal cortex. rTMS significantly reduced blood cortisol levels and decreased prolactinemia, thus suggesting dopamine increase. Craving visual analogic scale (VAS) in treated patients decreased, as well as mean number of alcoholic drinks/day and drinks on days of maximum alcohol intake (DMAI). In the sham group there was no significant effect observed on cortisolemia, prolactinemia, mean number of alcoholic drinks/day, or drinks/DMAI. Thus, deep rTMS could be considered a potential new treatment for alcoholism.
引用
收藏
页码:283 / 290
页数:8
相关论文
共 51 条
[1]
Repeated high-frequency transcranial magnetic stimulation over the dorsolateral prefrontal cortex reduces cigarette craving and consumption [J].
Amiaz, Revital ;
Levy, Dino ;
Vainiger, Dana ;
Grunhaus, Leon ;
Zangen, Abraham .
ADDICTION, 2009, 104 (04) :653-660
[2]
[Anonymous], 1992, Measuring Alcohol Consumption: Psychosocial and Biochemical Methods, DOI 10.1007/978-1-4612-0357-5_3
[3]
Besemer F, 2011, NETH J MED, V69, P318
[4]
Salivary cortisol on ROCHE Elecsys immunoassay system: pilot biological variation studies [J].
Chiu, SK ;
Collier, CP ;
Clark, AF ;
Wynn-Edwards, KE .
CLINICAL BIOCHEMISTRY, 2003, 36 (03) :211-214
[5]
The somatic marker hypothesis and the possible functions of the prefrontal cortex [J].
Damasio, AR .
PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES, 1996, 351 (1346) :1413-1420
[6]
The Loss of Metabolic Control on Alcohol Drinking in Heavy Drinking Alcohol-Dependent Subjects [J].
de Timary, Philippe ;
Cani, Patrice D. ;
Duchemin, Julie ;
Neyrinck, Audrey M. ;
Gihousse, Dominique ;
Laterre, Pierre-Francois ;
Badaoui, Abdenor ;
Leclercq, Sophie ;
Delzenne, Nathalie M. ;
Starkel, Peter .
PLOS ONE, 2012, 7 (07)
[7]
DIORIO D, 1993, J NEUROSCI, V13, P3839
[8]
Fahie-Wilson M, 2000, CLIN CHEM, V46, P1993
[9]
The medial prefrontal cortex differentially regulates stress-induced c-fos expression in the forebrain depending on type of stressor [J].
Figueiredo, HF ;
Bruestle, A ;
Bodie, B ;
Dolgas, CM ;
Herman, JP .
EUROPEAN JOURNAL OF NEUROSCIENCE, 2003, 18 (08) :2357-2364
[10]
Corticotropin-releasing factor within the central nucleus of the amygdala mediates enhanced ethanol self-administration in withdrawn, ethanol-dependent rats [J].
Funk, Cindy K. ;
O'Dell, Laura E. ;
Crawford, Elena F. ;
Koob, George F. .
JOURNAL OF NEUROSCIENCE, 2006, 26 (44) :11324-11332