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Is there a place for cellular therapy in depression?

World Journal of Psychiatry 2021年第9期11卷 553-567页

作者： Pedro Antonio Schmidt do Prado-Lima Zaquer Suzana Munhoz Costa-Ferro Bruno Solano de Freitas Souza ivana beatrice manica da cruz Biogenomics Lab Brain Institute of Rio Grande do Sul(BraIns) Pontifical Catholic University of Rio Grande do SulPorto Alegre 90610-000Rio Grande do SulBrazil Center for Biotechnology and Cell Therapy Sao Rafael HospitalSalvador 41253-190BahiaBrazil D’Or Institute for Research and Education(IDOR) Salvador 41253-190BahiaBrazil Laboratory of Tissue Engineering and Immunopharmacology Gonçalo Moniz InstituteFiocruzSalvador 40296-710BahiaBrazil Health Sciences Center Federal University of Santa MariaSanta Maria 97105900RSBrazil

Although efforts have been made to improve the pharmacological treatment of depression,approximately one-third of patients with depression do not respond to conventional therapy using *** potential non-pharmacological therapies have been studied in the last years,including the use of mesenchymal stem cell therapies to treat *** therapies are reviewed here since it is clinically relevant to develop innovative therapeutics to treat psychiatric *** data corroborate that mesenchymal stem cell therapy could be considered a potential treatment for depression based on its antiinflammatory and neurotrophic ***,some clinical trials involving treatment of depression with stem cells are in progress,but with no published *** studies and other future clinical investigations will be crucial to define how much mesenchymal stem cells can effectively be used in psychiatric clinics as a strategy for supporting depression treatment.

关键词： Mood disorders Stem cells transplant Mesenchymal stem-cells transplant Inflammation Immunomodulation Depression

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Impact of obesity and Ala16Val MnSOD polymorphism interaction on lipid, inflammatory and oxidative blood biomarkers

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Open Journal of Genetics 2012年第4期2卷 202-209页

作者： Maria Fernanda manica-Cattani Francine Carla Cadoná Raul de Oliveira Tális da Silva Alencar Kolinski Machado Fernanda Barbisan Marta Maria Medeiros Frescura Duarte ivana beatrice manica da cruz Biogenomic Laboratory Center of Science of Health Federal University of Santa Maria Santa Maria Brazil Post-Graduate Program in Pharmacology Federal University of Santa Maria Santa Maria Brazil Post-Graduate Program in Toxicology Biochemistry Federal University of Santa Maria Santa Maria Brazil

Previous investigations suggest association between obesity and Ala16Val MnSOD gene polymorphism. The V allele produces enzyme which not catalyze the superoxide anion efficiently as occurs with A allele. As obesity is related to development of other metabolic disorders we performed a study that analyzed the effect of interaction between Ala16Val MnSOD polymorphism and obesity on lipid, oxidative and inflammatory biomarkers of adult subjects. The study enrolled 161 volunteers as categorized in six groups with different genotypes: Obeses with different genotypes (AAO, VVO and AVO) and nonobese (AANO, VVNO and AVNO). In general the group AANO presented lower values whereas VVO presented higher values of biomarkers analyzed. These results suggest that oxidative metabolism influenced by genetic status could to minimize or maximize the obesity effects on lipid, oxidative and inflammatory biomarkers that are also implicated in the genesis of important dysfunctions and diseases as atherosclerosis, diabetes 2 and cardiovascular morbidities.

关键词： Ala16Val MnSOD Polymorphism Obesity Oxidative Stress Inflammation Oxidized LDL Anti-Oxidized LDL Hs-PCR

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Antidepressant Drugs Modulate Differentially Anti-inflammatory Lithium＇s Property： An in Vitro and in Vivo Study

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Journal of Pharmacy and Pharmacology 2018年第4期6卷 287-304页

作者： Femanda Barbisan Pedro Antonio Schmidt do Prado-Lima Veronica Farina Azzolin Maiquidieli dal Berto Claudia Giuliano Bica Cibele Ferreira Teixeira Dianni Capeleto Ivo Emilio da cruz Jung Euler Esteves Ribeiro Marta Maria Medeiros Frescura Duarte ivana beatrice manica da cruz Graduate Program in Pharmacology Federal University of Santa Maria Santa Maria-RS 97105900 Brazil Brain Institute Catholic University of Rio Grande do Sul Porto Alegre-RS 91410000 Brazil Graduate Program in Pathology Federal University of Health Sciences of Porto Alegre Porto Alegre-RS 90050170 Brazil Open University of the Third Age State University of Amazonas Manaus-AM 69029040 Brazil Lutheran University of Brazil Santa Maria-RS 97030080 Brazil

Li （lithium）, a mood stabilizer has anti-inflammatory effect. However, in clinical practice, Li can be administered together with other antidepressants drugs, such as FLX （fluoxetine）, IMI （imipramine）, NOR （nortriptyline） and ESC （escitalopram）. As interaction between Li and these antidepressant drugs on inflammatory modulation has not been investigated yet, we performed an in vitro protocol using a non-human macrophage cell line. Oxidative and inflammatory markers, as well as cell cycle analysis and cytokine gene expressions were compared among treatments. An IR （inflammatory ratio） was calculated based on the following oxidative-inflammatory variables： nitric oxide, superoxide anion, reactive oxygen molecules, cytokines IL-113, IL-6, TNF-ct and IL-10. The in vitro calculated IR data were validated through an in vivo analysis of 154 human subjects with similar IR. Li and control cells presented similar IR values. FLX, NOR and IMI increased slightly IR values indicating some proinflammatory effect, whereas ESC decreased IR values indicating some anti-inflammatory effect. However, cells exposed to Li ＋ ESC triggered a proinflammatory response on macrophages. Thus, IR comparison results suggest that the Li anti-inflammatory effect is not universal and could be influenced by both basal macrophage-inflammatory state and interaction of other psychiatric drugs. These results could be useful to understand some inconsistencies observed in human studies involving Li and other psychiatric drugs.

关键词： Mood disorders inflammation selective serotonin reuptake inhibitors bipolar disorder lithium.

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