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1.
Am J Physiol Regul Integr Comp Physiol ; 325(6): R759-R768, 2023 Dec 01.
Article in English | MEDLINE | ID: mdl-37842740

ABSTRACT

Animal data indicate that insulin triggers a robust nitric oxide synthase (NOS)-mediated dilation in cerebral arteries similar to the peripheral tissue vasodilation observed in healthy adults. Insulin's role in regulating cerebral blood flow (CBF) in humans remains unclear but may be important for understanding the links between insulin resistance, diminished CBF, and poor brain health outcomes. We tested the hypothesis that an oral glucose challenge (oral glucose tolerance test, OGTT), which increases systemic insulin and glucose, would acutely increase CBF in healthy adults due to NOS-mediated vasodilation, and that changes in CBF would be greater in anterior regions where NOS expression or activity may be greater. In a randomized, single-blind approach, 18 young healthy adults (24 ± 5 yr) underwent magnetic resonance imaging (MRI) with a placebo before and after an OGTT (75 g glucose), and 11 of these adults also completed an NG-monomethyl-l-arginine (l-NMMA) visit. Four-dimensional (4-D) flow MRI quantified macrovascular CBF and arterial spin labeling (ASL) quantified microvascular perfusion. Subjects completed baseline imaging with a placebo (or l-NMMA), then consumed an OGTT followed by MRI scans and blood sampling every 10-15 min for 90 min. Contrary to our hypothesis, total CBF (P = 0.17) and global perfusion (P > 0.05) did not change at any time point up to 60 min after the OGTT, and no regional changes were detected. l-NMMA did not mediate any effect of OGTT on CBF. These data suggest that insulin-glucose challenge does not acutely alter CBF in healthy adults.


Subject(s)
Enzyme Inhibitors , Nitric Oxide Synthase , Adult , Animals , Humans , omega-N-Methylarginine/pharmacology , Glucose Tolerance Test , Enzyme Inhibitors/pharmacology , Single-Blind Method , Cerebrovascular Circulation , Glucose/metabolism , Insulin/pharmacology
3.
Br J Clin Pharmacol ; 70(6): 881-5, 2010 Dec.
Article in English | MEDLINE | ID: mdl-21175443

ABSTRACT

AIMS: A QT-heart rate nomogram has recently been proposed as a means of identifying patients at risk of torsades de pointes after antidepressant overdose, based on published cases of drug-induced torsades de pointes. The present study sought to examine the performance of the nomogram in patients who ingest an antidepressant overdose but do not develop arrhythmia. METHODS: A retrospective case control study of patients presenting to hospital after overdose of citalopram, mirtazapine and venlafaxine was carried out. The primary outcome variable was QT higher than the nomogram, and was compared with occurrence of QT(c) (QT corrected by Bazett's formula) greater than ≥440 ms and QT(c) ≥500 ms, with comparison between drugs. Data are expressed as proportions in each group with 95% confidence intervals. RESULTS: There were 858 electrocardiograms from 541 patients. QT was higher than the nomogram in 2.4% (1.4, 4.1%), whereas QT(c) was ≥440 ms in 23.1% (95% CI 19.8, 26.8%), and QT(c) was ≥500 ms in 1.1% (0.5, 2.5%). Citalopram overdose was more likely to be associated with QT higher than the nomogram compared with the other agents (difference 7.0%, 95% CI 2.9, 11.9%, P = 0.001) and more likely to be associated with QT(c) ≥440 ms (difference = 11.0%, 95% CI 2.6, 19.0%, P = 0.013). CONCLUSIONS: The QT nomogram was associated with a lower false positive rate than widely accepted QT(c) criteria, and allowed detection of different effects of individual drugs. The nomogram offers potential advantages over QT(c) criteria and merits further investigation in a clinical setting.


Subject(s)
Antidepressive Agents/poisoning , Long QT Syndrome/diagnosis , Nomograms , Adult , Citalopram/poisoning , Cyclohexanols/poisoning , Drug Overdose , Electrocardiography/methods , Female , Heart Rate/drug effects , Humans , Long QT Syndrome/chemically induced , Male , Mianserin/analogs & derivatives , Mianserin/poisoning , Mirtazapine , Retrospective Studies , Risk Assessment/methods , Torsades de Pointes/chemically induced , Torsades de Pointes/diagnosis , Venlafaxine Hydrochloride
4.
WMJ ; 108(7): 370-2, 2009 Oct.
Article in English | MEDLINE | ID: mdl-19886586

ABSTRACT

BACKGROUND: The etiology of isolated right ventricular hypertrophy (RVH) is distinct from other forms of hypertrophic cardiomyopathy. RVH is typically seen in the setting of pulmonary valve stenosis or Tetralogy of Fallot. A rare cause of isolated RVH is premature closure of the patent ductus arteriosus (PDA) in utero that results in pulmonary hypertension. This can have a range of outcomes, from spontaneous resolution to fetal demise. METHODS: This case report describes a term infant who presented with respiratory distress and striking isolated RVH, pulmonary hypertension, and no PDA. She was treated conservatively with supplemental oxygen. RESULTS: The patient was gradually weaned off oxygen over the course of two weeks and follow-up echocardiography showed resolution of her RVH and pulmonary hypertension by 14 weeks of age. CONCLUSIONS: The presentation and course of this patient with severe isolated RVH is consistent with spontaneous premature closure of the ductus arteriosus in utero.


Subject(s)
Ductus Arteriosus, Patent/complications , Hypertrophy, Right Ventricular/etiology , Ductus Arteriosus, Patent/diagnostic imaging , Echocardiography , Female , Humans , Hypertrophy, Right Ventricular/diagnostic imaging , Infant, Newborn , Pregnancy
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