Human Cerebral Blood Flow and Serotonin

Depression Clinical Trial

Official title: Human Cerebral Blood Flow and Serotonin

Status Not yet recruiting

Clinical Trial Summary

Breathing, blood pressure, and blood flow into the brain are controlled - in part - by small areas in the brainstem; the central chemoreceptors. The mechanisms involved in the transmission of signals through the brainstem and also in controlling brain blood flow past the brainstem both use a molecule called serotonin. Citalopram is a "selective serotonin reuptake inhibitor" (or SSRI) which means it allows serotonin to be released in the brain but stops it from being reabsorbed. SSRIs are often used as antidepressants. This study aims to investigate the influence of an SSRI on the control of brain blood flow.

Clinical Trial Description

PURPOSE To determine the influence of acute selective serotonin reuptake inhibition (SSRI) on cerebrovascular function in humans

HYPOTHESIS We hypothesize that SSRI will not impact CO2 reactivity (a measure of cerebral vascular function); will reduce neurovascular coupling (a measure of regional cerebral metabolism regulation of the vasculature), and will augment the ventilatory response to CO2 (a measure of brainstem chemosensitivity).

Justification:

There is ample evidence in animal models that the neurotransmitter serotonin (5-hydroxytryptamine; 5-HT) is an integral component in neuronal signalling in areas of the brainstem controlling ventilation, and that such 5-HT neurons directly innervate blood vessels and astrocytes (brain cells controlling blood flow) in the brainstem. Brainstem areas, in particular those of the raphe nuclei, containing 5-HT neurons, have been implicated as being actively involved with cerebral microvascular regulation. Extensive preclinical evidence suggests that 5-HT contributes directly to neurogenic control of the vascular beds surrounding raphe nuclei due to neuronal 5-HT release. Furthermore, increases in 5-HT can lead to an uncoupling of CBF and cerebral metabolism.

Increased 5-HT release or availability (e.g., through inhibition of reuptake) leads to a decrease in the relationship between CBF and cerebral metabolism, potentially indicating and impairment in the cerebral vasculature to respond to the needs of brain.

In humans, oral buspirone (a partial 5-HT agonist) decreases CBF in regions of the posterior cingulate while m-CPP (mixed 5-HT agonist/antagonist) increases the cerebral metabolic utilization of glucose (CMRglu) in several regions. Increases in CMRglu of 4% to 5% in the prefrontal cortex and relative decreases of 3% in occipitotemporal regions occur during oral fenfluramine (a 5-HT analogue; increases extracellular serotonin levels). Increases in CBF in the bilateral frontal cortex but decreases within the bilateral temporal cortex and left thalamus also occur in response to intravenous fenfluramine. Oral fenfluramine increases CMRglu in left prefrontal regions but CMRglu decreases in right hemispheric regions. Paroxetine - a commonly prescribed selective serotonin reuptake inhibitor (SSRI) - reduces resting cerebral perfusion especially in the brainstem. Finally, CMRglu is reduced in parts of the amygdala, hippocampus and striatum, and increases in the right superior parietal lobe, following oral fluoxetine. In summary, there is certainly modification of both CBF and CMRO2 with 5-HT perturbations, however, it is unclear whether cerebral vascular regulation per se is affected.

Intravenous infusion of ketanserin - a drug used to treat hypertension with its adrenergic receptor inhibition properties which also has some selective 5-HT2A receptor antagonist properties - is reported to have little effect on basal CBF, or cerebral defence against variations in partial pressure of arterial carbon dioxide (PaCO2) or blood pressure, but does reduce whole-brain cerebral O2 metabolism. However, ketanserin also elicits hypotension (lowered mean arterial pressure) that confounds analyses of CBF responses if not accounted for. Although serotonin per se has some vasoconstrictive effects, true SSRIs have little to no effects on blood pressure in humans, as such, it is difficult to assign these effects purely 5-HT related effects.

Serotonin is transported in circulation bound to platelets, and the release of this platelet-bound 5-HT is associated with increased immune responses (release of interleukin-6) from the vasculature. As such, there is precedent to assess the effects of SSRIs on platelet-bound and free plasma 5-HT, as well as adrenal cortisol secretion and immunological responses across the brain. This is relevant to the acute impacts of SSRIs on factors that contribute to lifetime cardiovascular health.

Almost 1 in 4 Canadians will suffer depression in the course of their lives. Although there has been recent dissention regarding the association between serotonin and depression , the prevalence of SSRIs is undeniable. Of North American adults diagnosed with depression, 61.6% use SSRIs; while between 2015 to 2018, ~13% of North Americans older than 18 reported taking antidepressant medications. Citalopram, a highly selective 5-HT reuptake inhibitor was has been prescribed to >30 million patients in >70 countries. Given the prevalence of SSRIs and the potential implications that 5-HT related neurovascular dysregulation may have for cerebral vascular function (and ventilation control and blood pressure control given the importance of 5-HT signalling in the brainstem) it is surprising that so little work has investigated the cerebral effects. There is little work in humans assessing the activity of serotonin in dynamic regulation of CBF. Cerebral responses to the five main drivers for which CBF is regulated [i.e., O2, CO2, mean arterial blood pressure, cerebral metabolism, and autonomic control], represent the functional reactivity of the cerebral vasculature. Measurement of these outcomes can give insight in to a number of vascular mechanisms and are widely used in research and clinical settings.

Although several studies have assessed basal steady state CBF and CMRO2 during 5-HT perturbations, none have investigated the effects of SSRI administration on cerebral vascular function as none have used CBF measurement techniques with sufficient temporal resolution to do so.

Research Design:

This study will be performed at the Centre for Heart, Lung and Vascular Health at the UBC Okanagan Campus. Participants will visit the laboratory on three occasions, the first of which should last ~30 minutes and rest of which should last no more than ~7 hours each; altogether totalling ~14.5 hours.

The first visit will consist of a familiarization visit wherein participants will be given all information regarding the study, and, should they give informed consent, will then have both ICAs and both VAs scanned using duplex ultrasound to assess patency of reliable images. Following the familiarisation, participants will visit the laboratory on two occasions, to undergo experimental visits which will include: a placebo visit and an SSRI visit. So that we can ensure full washout of SSRI between visits, the two experimental visits will be scheduled one week apart in males and one month apart in females (to account for menstrual cycle).

All participants will undergo all experimental sessions, in randomized, counterbalanced order. Participants will not be informed of which drug was received during which session until after the completion of the entire experimental study. Upon completion of informed written consent and the health questionnaire (submitted alongside this application) participants will be familiarized to the measurements and equipment.

STATISTICAL ANALYSES Differences in pre vs post test responses between visits will be examined using linear mixed modal analysis. Between-day variability of baseline responses will be examined using paired two-tailed T-tests. Repeatability between days within-subjects will be determined using Pearson's (r) and intraclass correlation coefficients (ICC2,1: two-way random effects, absolute agreement, single rater/measurement. Within-subjects coefficients of variation will be calculated for between-day assessments.

SAMPLE SIZE JUSTIFICATION There are no previous studies upon which to base a priori power calculations. As such, we estimate, based on previous studies from our laboratory assessing the same outcomes pre vs post other pharmacological interventions, that we will be adequately powered to see changes in cerebral variables from baseline with a sample size of n=~15. ;

Related Conditions & MeSH terms

• Depression

• NCT number: NCT05957094
• Study type: Interventional
• Source: University of British Columbia
• Contact: Jay Carr, PhD
• Phone: 2508596365
• Email: jcarr@student.ubc.ca
• Status: Not yet recruiting
• Phase: N/A
• Start date: August 2023
• Completion date: August 2024