Methylphenidate-induced changes in regional cerebral blood flow: A [15O]H2O PET study in healthy volunteers

2005 ◽  
Vol 25 (1_suppl) ◽  
pp. S340-S340
Author(s):  
Joanna I Udo de Haes ◽  
Paul Maguire ◽  
Anne M J Paans ◽  
Piet L Jager ◽  
Johan A den Boer
2017 ◽  
Vol 31 (7) ◽  
pp. 553-562
Author(s):  
Nobuhiro Yada ◽  
Hideo Onishi ◽  
Masahiro Miyai ◽  
Kentarou Ozasa ◽  
Takashi Katsube ◽  
...  

Cephalalgia ◽  
2005 ◽  
Vol 25 (5) ◽  
pp. 344-352 ◽  
Author(s):  
LH Lassen ◽  
B Sperling ◽  
AR Andersen ◽  
J Olesen

The aim of this study was to estimate the effect of Nitric Oxide synthase (NOS)-inhibition (L-NMMA) on the diameter of the middle cerebral artery (MCA) and on regional cerebral blood flow (rCBF). Furthermore, to assess the effect of L-NMMA on acetazolamide induced increases in MCA blood velocity (Vmean) and rCBF. In an open crossover design 12 healthy subjects attended the laboratory twice. The first day 6 mg/kg L-LNMMA i.v. over 15 min preceded 1 g acetazolamide iv over 5 min. Eight days later only acetazolamide was given. Vmean in MCA was determined with transcranial Doppler (TCD) and rCBF with Xe-133 inhalation SPECT at baseline, after L-NMMA and 25 and 55 min after acetazolamide infusion. After L-NMMA the decrease in rCBFMCA was 6.8% (± 7.4) ( P < 0.019, n = 12), whereas Vmean was not affected ( P = 0.83, n = 8). The change in MCA diameter was estimated to -1.3% ( P = 0.44, n = 8). L-NMMA did not affect acetazolamide increases in Vmean ( P = 0.67, n = 8) nor rCBF ( P = 0.29, n = 12). The percentage increase of Vmean was 1.5 times that of rCBF ( n = 8). Our data suggest that the basal tone of human cerebral arterioles but not of conduit arteries is NO-dependent. The action of acetazolamide in man is not NO-dependent.


2010 ◽  
Vol 25 (4) ◽  
pp. 255-260 ◽  
Author(s):  
Kazunari Ishii ◽  
Takafumi Uemura ◽  
Naokazu Miyamoto ◽  
Toshiki Yoshikawa ◽  
Toshiaki Yamaguchi ◽  
...  

2019 ◽  
Author(s):  
D. A. Martins ◽  
N. Mazibuko ◽  
F. Zelaya ◽  
S. Vasilakopoulou ◽  
J. Loveridge ◽  
...  

ABSTRACTCould nose-to-brain pathways mediate the effects of peptides such as oxytocin (OT) on brain physiology when delivered intranasally? We address this question by contrasting two methods of intranasal administration (a standard nasal spray, and a nebulizer expected to improve OT deposition in nasal areas putatively involved in direct nose-to-brain transport) to intravenous administration in terms of effects on regional cerebral blood flow during two hours post-dosing. We demonstrate that OT-induced decreases in amygdala perfusion, a key hub of the OT central circuitry, are explained entirely by OT increases in systemic circulation following both intranasal and intravenous OT administration. Yet we also provide robust evidence confirming the validity of the intranasal route to target specific brain regions. Our work has important translational implications and demonstrates the need to carefully consider the method of administration in our efforts to engage specific central oxytocinergic targets for the treatment of neuropsychiatric disorders.


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