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      Antihypertensive drugs and brain function: mechanisms underlying therapeutically beneficial and harmful neuropsychiatric effects

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          Abstract

          A bidirectional relationship exists between hypertension and psychiatric disorders, including unipolar and bipolar depression, anxiety, post-traumatic stress disorder (PTSD), psychosis, schizophrenia, mania, and dementia/cognitive decline. Repurposing of antihypertensive drugs to treat mental disorders is thus being explored. A systematic knowledge of the mechanisms of action and clinical consequences of the use of antihypertensive agents on neuropsychiatric functions has not been achieved yet. In this article, we review the putative role of antihypertensive agents in psychiatric disorders, discuss the targets and mechanisms of action, and examine how and to what extent specific drug classes/molecules may trigger, worsen, or mitigate psychiatric symptoms. In addition, we review pharmacokinetics (brain penetration of drugs) and pharmacogenetics data that add important information to assess risks and benefits of antihypertensive drugs in neuropsychiatric settings.

          The scientific literature shows robust evidence of a positive effect of α1 blockers on PTSD symptoms, nightmares and sleep quality, α2 agonists on core symptoms, executive function, and quality of life in Attention-Deficit/Hyperactivity Disorder, PTSD, Tourette’s syndrome, and β blockers on anxiety, aggression, working memory, and social communication. Renin-angiotensin system modulators exert protective effects on cognition, depression, and anxiety, and the loop diuretic bumetanide reduced the core symptoms of autism in a subset of patients. There is no evidence of clear benefits of calcium channel blockers in mood disorders in the scientific literature. These findings are mainly from preclinical studies; clinical data are still insufficient or of anecdotal nature and seldom systematic. The information herewith provided can support a better therapeutic approach to hypertension, tailored to patients with, or with high susceptibility to, psychiatric illness. It may prompt clinical studies exploring the potential benefit of antihypertensive drugs in selected patients with neuropsychiatric comorbidities that include outcomes of neuropsychiatric interest and specifically assess undesirable effects or interactions.

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          Most cited references318

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          Biological Insights From 108 Schizophrenia-Associated Genetic Loci

          Summary Schizophrenia is a highly heritable disorder. Genetic risk is conferred by a large number of alleles, including common alleles of small effect that might be detected by genome-wide association studies. Here, we report a multi-stage schizophrenia genome-wide association study of up to 36,989 cases and 113,075 controls. We identify 128 independent associations spanning 108 conservatively defined loci that meet genome-wide significance, 83 of which have not been previously reported. Associations were enriched among genes expressed in brain providing biological plausibility for the findings. Many findings have the potential to provide entirely novel insights into aetiology, but associations at DRD2 and multiple genes involved in glutamatergic neurotransmission highlight molecules of known and potential therapeutic relevance to schizophrenia, and are consistent with leading pathophysiological hypotheses. Independent of genes expressed in brain, associations were enriched among genes expressed in tissues that play important roles in immunity, providing support for the hypothesized link between the immune system and schizophrenia.
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            Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis

            The Lancet, 381(9875), 1371-1379
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              Stress signalling pathways that impair prefrontal cortex structure and function.

              The prefrontal cortex (PFC) - the most evolved brain region - subserves our highest-order cognitive abilities. However, it is also the brain region that is most sensitive to the detrimental effects of stress exposure. Even quite mild acute uncontrollable stress can cause a rapid and dramatic loss of prefrontal cognitive abilities, and more prolonged stress exposure causes architectural changes in prefrontal dendrites. Recent research has begun to reveal the intracellular signalling pathways that mediate the effects of stress on the PFC. This research has provided clues as to why genetic or environmental insults that disinhibit stress signalling pathways can lead to symptoms of profound prefrontal cortical dysfunction in mental illness.
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                Author and article information

                Contributors
                Journal
                Cardiovasc Res
                Cardiovasc Res
                cardiovascres
                Cardiovascular Research
                Oxford University Press (US )
                0008-6363
                1755-3245
                March 2023
                28 July 2022
                28 July 2022
                : 119
                : 3
                : 647-667
                Affiliations
                Unit of Clinical Pharmacology, Department of Biomedical and Clinical Sciences (DIBIC), ASST Fatebenefratelli-Sacco University Hospital, Università degli Studi di Milano , Via GB Grassi 74, 20157 Milano, Italy
                Unit of Clinical Pharmacology, Department of Biomedical and Clinical Sciences (DIBIC), ASST Fatebenefratelli-Sacco University Hospital, Università degli Studi di Milano , Via GB Grassi 74, 20157 Milano, Italy
                Unit of Clinical Pharmacology, ASST Fatebenefratelli-Sacco University Hospital , 20157 Milano, Italy
                Unit of Clinical Pharmacology, ASST Fatebenefratelli-Sacco University Hospital , 20157 Milano, Italy
                Unit of Clinical Pharmacology, ASST Fatebenefratelli-Sacco University Hospital , 20157 Milano, Italy
                Unit of Brain-Heart Axis: Cellular and Molecular Mechanisms – Centro Cardiologico Monzino IRCCS , 20138 Milano, Italy
                Unit of Vascular Biology and Regenerative Medicine – Centro Cardiologico Monzino IRCCS , 20138 Milan, Italy
                Department of Biomedical, Surgical and Dental Sciences, Università degli Studi di Milano , 20122 Milan, Italy
                Scientific Institute IRCCS Eugenio Medea , 23842 Bosisio Parini (LC), Italy
                Unit of Clinical Pharmacology, Department of Biomedical and Clinical Sciences (DIBIC), ASST Fatebenefratelli-Sacco University Hospital, Università degli Studi di Milano , Via GB Grassi 74, 20157 Milano, Italy
                Scientific Institute IRCCS Eugenio Medea , 23842 Bosisio Parini (LC), Italy
                Scientific Institute IRCCS Eugenio Medea , 23842 Bosisio Parini (LC), Italy
                Author notes
                Corresponding author. Tel +39 02 50319643; fax: +39 02 50319682, E-mail: emilio.clementi@ 123456unimi.it

                C.C. and C.P. contributed equally to the manuscript.

                E.C. and M.P. are joint last authors.

                Conflict of interest: none declared.

                Author information
                https://orcid.org/0000-0002-4107-196X
                https://orcid.org/0000-0001-6680-4536
                https://orcid.org/0000-0003-2389-7191
                https://orcid.org/0000-0003-1512-6530
                https://orcid.org/0000-0002-8276-3663
                https://orcid.org/0000-0002-7486-2637
                https://orcid.org/0000-0003-2581-5735
                https://orcid.org/0000-0002-3910-6836
                https://orcid.org/0000-0001-7333-8270
                https://orcid.org/0000-0002-3800-5697
                Article
                cvac110
                10.1093/cvr/cvac110
                10153433
                35895876
                b1ae2f58-8133-4ef9-8fb2-5a1127120534
                © The Author(s) 2022. Published by Oxford University Press on behalf of the European Society of Cardiology.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 29 December 2021
                : 15 June 2022
                : 21 June 2022
                : 06 August 2022
                Page count
                Pages: 21
                Funding
                Funded by: Italian Ministry of Health, doi 10.13039/501100003196;
                Categories
                Invited Review
                AcademicSubjects/MED00200

                Cardiovascular Medicine
                antihypertensive drugs,neuropsychiatric disorders,personalized medicine

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