Role of turmeric and cinnamon spices in digestive, metabolic, and immune systems

Введение. Коронавирус SARS-CoV-2 является новым вирусом, обладающим способностью осуществлять трансмиссию воздушно-капельным путем, вызывая тяжелое течение атипичной пневмонии, нередко сочетающейся с коагулопатиями. Роль структурных белков коронавируса в их патогенезе неизвестна. Цель исследования: с помощью биоинформационного анализа выявить в структурных белках коронавируса SARS-CoV-2 последовательности, гомологичные белкам системы гемостаза, и рассмотреть возможные сценарии их участия в патогенезе коагулопатий при COVID-19, а также объяснить существование вирусостатического эффекта гепарина. Материалы и методы. Для компьютерного анализа были использованы доступные в Интернете базы данных первичных структур белков коронавирусов и их рецепторов, а также поверхностных белков других вирусов, белков системы гемостаза и иммунной системы. Сравнивали аминокислотный состав белков и распределение оснόвных аминокислот (аргинина и лизина) в их первичных последовательностях. С целью выявления пептидного (иммуноэпитопного) родства структурных белков коронавирусов с белками системы гемостаза человека был выполнен поиск гомологичных последовательностей в их белках. Результаты. В структурных белках коронавируса SARS-CoV-2 выявлено множество последовательностей, гомологичных белкам системы гемостаза и иммунной системы. В отличие от коронавирусов SARS-CoV и MERS-CoV, S1-субъединица S-белка коронавируса SARS-CoV-2 имеет положительную полярность. Заключение. Множество последовательностей в структурных белках коронавируса SARS-CoV-2, гомологичных белкам системы гемостаза, потенциально способны вы- зывать различные сценарии патогенеза коагулопатий. Положительная полярность S1-субъединицы S-белка коронавируса SARS-CoV-2 позволяет объяснить неспецифическое взаимодействие ее с гепарином и его вирусостатический (неантикоагулянтный) эффект. Background. The coronavirus SARS-CoV-2 is a new virus capable of human-human transmission and inducing a severe atypical pneumonia often associated with coagulopathy. A role of SARS-CoV-2 structural proteins in coagulopathy pathogenesis is unknown. Objectives: to use a bioinformation analysis to identify SARS-CoV-2 sequences in the structural proteins that are homologous to hemostasis system proteins, regard their possible participation in coagulopathy pathogenesis and explain the antiviral effect of heparin. Materials / Methods. For computer analysis, Internet databases were used of the primary structures of coronavirus proteins and their receptors, as well as surface proteins of other viruses, proteins of hemostasis and immune systems. The amino acid composition of proteins and the distribution of basic amino acids (arginine and lysine) in their primary sequences were compared. For detection of peptide (immunoepitopic) relationship of coronaviruses structural proteins with human hemostasis proteins, a search for homologous sequences in their proteins was performed. Results. Many sequences have been identified in structural proteins of SARS-CoV-2 coronavirus that are homologous to the proteins of hemostasis and immune systems. In contrast with SARS-CoV and MERS-CoV coronaviruses, the S1-subunit of SARS-CoV-2 coronavirus S-protein has a positive polarity. Conclusions. Many sequences in SARS-CoV-2 structural proteins that homologous to hemostasis system proteins are potentially responsible for coagulopathy pathogenesis. The positive polarity of the S1-subunit of SARS-CoV-2 S-protein explains its nonspecific interaction with heparin and its virostatic (non-anticoagulant) effect.

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Immunotoxicity of Xenobiotics in Fish: A Role for the Aryl Hydrocarbon Receptor (AhR)?

International Journal of Molecular Sciences ◽

10.3390/ijms22179460 ◽

2021 ◽

Vol 22 (17) ◽

pp. 9460

Author(s):

Helmut Segner ◽

Christyn Bailey ◽

Carolina Tafalla ◽

Jun Bo

Keyword(s):

Immune System ◽

Aryl Hydrocarbon Receptor ◽

Disease Susceptibility ◽

Immune Cell ◽

Physiological Role ◽

Immune Gene ◽

Immune Systems ◽

Aryl Hydrocarbon ◽

The Impact

The impact of anthropogenic contaminants on the immune system of fishes is an issue of growing concern. An important xenobiotic receptor that mediates effects of chemicals, such as halogenated aromatic hydrocarbons (HAHs) and polyaromatic hydrocarbons (PAHs), is the aryl hydrocarbon receptor (AhR). Fish toxicological research has focused on the role of this receptor in xenobiotic biotransformation as well as in causing developmental, cardiac, and reproductive toxicity. However, biomedical research has unraveled an important physiological role of the AhR in the immune system, what suggests that this receptor could be involved in immunotoxic effects of environmental contaminants. The aims of the present review are to critically discuss the available knowledge on (i) the expression and possible function of the AhR in the immune systems of teleost fishes; and (ii) the impact of AhR-activating xenobiotics on the immune systems of fish at the levels of immune gene expression, immune cell proliferation and immune cell function, immune pathology, and resistance to infectious disease. The existing information indicates that the AhR is expressed in the fish immune system, but currently, we have little understanding of its physiological role. Exposure to AhR-activating contaminants results in the modulation of numerous immune structural and functional parameters of fish. Despite the diversity of fish species studied and the experimental conditions investigated, the published findings rather uniformly point to immunosuppressive actions of xenobiotic AhR ligands in fish. These effects are often associated with increased disease susceptibility. The fact that fish populations from HAH- and PAH-contaminated environments suffer immune disturbances and elevated disease susceptibility highlights that the immunotoxic effects of AhR-activating xenobiotics bear environmental relevance.

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Neuroimmunology for the Non-Immunologist

Neuroimmunology ◽

10.1093/med/9780190050801.003.0002 ◽

2019 ◽

pp. 2-20

Author(s):

Bibiana Bielekova

Keyword(s):

Immune System ◽

Antigen Presentation ◽

Immune Tolerance ◽

Short Introduction ◽

Immune Synapse ◽

Immune Systems ◽

Adaptive Immune ◽

Adaptive Immune Systems ◽

Autoimmune Phenomena

The chapter begins with a short introduction to the components of the immune system, outlining both the innate and adaptive components. It discusses the role of the immune system in protecting against infections and abnormal tissues. It describes the concepts of self-antigens, antigen presentation, and immune synapse. It then examines immune tolerance and the differing functions and capacities of the innate and adaptive immune systems. Finally, the chapter considers infections and autoimmune phenomena and how the immune system responds to these challenges.

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The role of multiple stressors in ranavirus-caused amphibian mortalities in Acadia National Park wetlands

Canadian Journal of Zoology ◽

10.1139/z09-124 ◽

2010 ◽

Vol 88 (1) ◽

pp. 108-121 ◽

Cited By ~ 17

Author(s):

M. K. Gahl ◽

A.J.K. Calhoun

Keyword(s):

National Park ◽

Multiple Stressors ◽

Disease Incidence ◽

Information Criterion ◽

Acadia National Park ◽

Free Living ◽

Immune Systems ◽

Physical Chemical ◽

Components Analysis

Recent studies suggest that multiple sublethal stressors compromise amphibian immune systems and increase susceptibility to disease. We examined two aspects of multiple stressors and incidence of ranavirus-caused amphibian mortalities in free-living amphibian populations: (1) among-pond differences in physical, chemical, and biological stressors that may exacerbate mortality events, and (2) temporal changes in within-pond stressors that coincide with mortality events. At the among-pond scale, we used principal components analysis and logistic regression followed by Akaike’s information criterion (QAICc) to identify stressors associated with disease incidence. Of the stressors we investigated, aluminum, temperature, and conductivity were most correlated with outbreaks, but it was unclear whether they increased ranavirus-caused mortality events. Sublethal stressors were difficult to isolate in the field and few were significantly associated with ranavirus across all breeding ponds. Our results suggest that each wetland, because of varied physical, biological, and chemical settings, will have its own suite of stressors that sublethally affect amphibians.

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Emerging evidence for a similar role of glutamate receptors in the nervous and immune systems

Journal of Neurochemistry ◽

10.1111/j.1471-4159.2005.03456.x ◽

2005 ◽

Vol 95 (4) ◽

pp. 913-918 ◽

Cited By ~ 75

Author(s):

Alexander A. Boldyrev ◽

David O. Carpenter ◽

Peter Johnson

Keyword(s):

Glutamate Receptors ◽

Immune Systems ◽

Similar Role

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Nitrogen(II) Oxide (Nitric Oxide, NO): Its Origin, Fate and Physiological Significance. A Review

Collection of Czechoslovak Chemical Communications ◽

10.1135/cccc19971355 ◽

1997 ◽

Vol 62 (9) ◽

pp. 1355-1383 ◽

Cited By ~ 4

Author(s):

Petr Vetrovsky ◽

Gustav Entlicher

Keyword(s):

Nitric Oxide ◽

Superoxide Anion ◽

De Novo ◽

Soluble Guanylate Cyclase ◽

No Synthase ◽

Transcriptional Level ◽

Immune Systems ◽

Important Target ◽

Target Molecules

The nitrogen oxide (NO), a free radical molecule, plays a key role in the regulation of mammalian physiology and pathophysiology, e.g., in cardiovascular, nervous or immune systems. This molecule is produced from guanidino moiety of amino acid L-arginine with NG-hydroxy-L-arginine as intermediate and L-citrulline as a co-product of this reaction. This conversion is catalyzed by an ezyme called NO-synthase. The NO-synthase belongs to the cytochrome P450 superfamily and four its isoenzymes are known so far. Two (denoted NOS-I and III) are constitutive, generate lower amounts (pmol) of NO and are regulated by Ca++/calmodulin system. The others (NOS-II and IV) are inducible, produce a larger quantity of NO (nmol) and are regulated at a transcriptional level. The constitutive form is present, for example, in endothelial and neuronal cells whereas the inducible form is de novo synthesized as a consequence of certain stimuli (including cytokines) in macrophages, vascular smooth muscle cells and other cells. There are several target molecules for NO depending on cells. The most frequent target is supposed to be the soluble guanylate cyclase. However, superoxide anion is a very important target for NO, too. The reaction between these two molecules leads to the production of peroxynitrite, the fate of which depends on environmental conditions. Therefore, the importance of this reaction is still debated. This review deals with the nature of NO, the mechanisms of its production, the role of intermediate NG-hydroxy-L-arginine and summarizes the biology of superoxide anion with respect to its reaction with NO. A review with 218 references.

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Protective and anti-inflammatory effects of acetylcholine in the heart

AJP Cell Physiology ◽

10.1152/ajpcell.00315.2020 ◽

2020 ◽

Author(s):

Cibele Rocha-Resende ◽

Aristobolo Mendes da Silva ◽

Marco A. M. Prado ◽

Silvia Guatimosim

Keyword(s):

Cholinergic System ◽

Inflammatory Cells ◽

Cardiac Diseases ◽

Immune Systems ◽

Cardiac Inflammation ◽

Adaptive Immune ◽

Protective Actions ◽

Cholinergic Signaling ◽

Adaptive Immune Systems

The innate and adaptive immune systems play an important role in the development of cardiac diseases. Therefore, it has become critical to identify molecules that can modulate inflammation in the injured heart. In this regard, activation of the cholinergic system in animal models of heart disease has been shown to exert protective actions that include immunomodulation of cardiac inflammation. In this mini-review, we briefly present our current understanding on the cardiac cellular sources of acetylcholine (ACh) (neuronal versus nonneuronal), followed by a discussion on its contribution to the regulation of inflammatory cells. Although the mechanism behind ACh-mediated protection still remains to be fully elucidated, the beneficial immunomodulatory role of the cholinergic signaling emerges as a potential key regulator of cardiac inflammation.

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The Functional Significance of Endocrine-immune Interactions in Health and Disease

Current Protein and Peptide Science ◽

10.2174/1389203720666191106113435 ◽

2020 ◽

Vol 21 (1) ◽

pp. 52-65

Author(s):

Sridhar Muthusami ◽

Balasubramanian Vidya ◽

Esaki M Shankar ◽

Jamuna Vadivelu ◽

Ilangovan Ramachandran ◽

...

Keyword(s):

Immune System ◽

Cell Differentiation ◽

Amino Acid ◽

Functional Role ◽

Immune Cell ◽

Amino Acid Derivatives ◽

Endocrine Glands ◽

Immune Systems ◽

Health And Disease

Hormones are known to influence various body systems that include skeletal, cardiac, digestive, excretory, and immune systems. Emerging investigations suggest the key role played by secretions of endocrine glands in immune cell differentiation, proliferation, activation, and memory attributes of the immune system. The link between steroid hormones such as glucocorticoids and inflammation is widely known. However, the role of peptide hormones and amino acid derivatives such as growth and thyroid hormones, prolactin, dopamine, and thymopoietin in regulating the functioning of the immune system remains unclear. Here, we reviewed the findings pertinent to the functional role of hormone-immune interactions in health and disease and proposed perspective directions for translational research in the field.

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