Multiple Aspects of Inappropriate Action of Renin-Angiotensin, Vasopressin, and Oxytocin Systems in Neuropsychiatric and Neurodegenerative Diseases.
Ewa Szczepanska-SadowskaAgnieszka WsolAgnieszka Cudnoch-JedrzejewskaKatarzyna CzarzastaTymoteusz ZeraPublished in: Journal of clinical medicine (2022)
The cardiovascular system and the central nervous system (CNS) closely cooperate in the regulation of primary vital functions. The autonomic nervous system and several compounds known as cardiovascular factors, especially those targeting the renin-angiotensin system (RAS), the vasopressin system (VPS), and the oxytocin system (OTS), are also efficient modulators of several other processes in the CNS. The components of the RAS, VPS, and OTS, regulating pain, emotions, learning, memory, and other cognitive processes, are present in the neurons, glial cells, and blood vessels of the CNS. Increasing evidence shows that the combined function of the RAS, VPS, and OTS is altered in neuropsychiatric/neurodegenerative diseases, and in particular in patients with depression, Alzheimer's disease, Parkinson's disease, autism, and schizophrenia. The altered function of the RAS may also contribute to CNS disorders in COVID-19. In this review, we present evidence that there are multiple causes for altered combined function of the RAS, VPS, and OTS in psychiatric and neurodegenerative disorders, such as genetic predispositions and the engagement of the RAS, VAS, and OTS in the processes underlying emotions, memory, and cognition. The neuroactive pharmaceuticals interfering with the synthesis or the action of angiotensins, vasopressin, and oxytocin can improve or worsen the effectiveness of treatment for neuropsychiatric/neurodegenerative diseases. Better knowledge of the multiple actions of the RAS, VPS, and OTS may facilitate programming the most efficient treatment for patients suffering from the comorbidity of neuropsychiatric/neurodegenerative and cardiovascular diseases.
Keyphrases
- wild type
- blood brain barrier
- cardiovascular disease
- systematic review
- coronavirus disease
- end stage renal disease
- induced apoptosis
- depressive symptoms
- autism spectrum disorder
- healthcare
- bipolar disorder
- neuropathic pain
- spinal cord
- working memory
- sars cov
- chronic pain
- mental health
- social media
- drug delivery
- newly diagnosed
- signaling pathway
- type diabetes
- chronic kidney disease
- prognostic factors
- pain management
- ejection fraction
- coronary artery disease
- cancer therapy
- genome wide
- intellectual disability
- oxidative stress
- multiple sclerosis
- cell death
- white matter
- sleep quality
- cardiovascular risk factors
- patient reported outcomes
- replacement therapy
- pi k akt