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  1. Article ; Online: Beyond epithelial damage: vascular and endothelial contributions to idiopathic pulmonary fibrosis.

    May, James / Mitchell, Jane A / Jenkins, R Gisli

    The Journal of clinical investigation

    2023  Volume 133, Issue 18

    Abstract: Idiopathic pulmonary fibrosis (IPF) is a progressive scarring disease of the lung with poor survival. The incidence and mortality of IPF are rising, but treatment remains limited. Currently, two drugs can slow the scarring process but often at the ... ...

    Abstract Idiopathic pulmonary fibrosis (IPF) is a progressive scarring disease of the lung with poor survival. The incidence and mortality of IPF are rising, but treatment remains limited. Currently, two drugs can slow the scarring process but often at the expense of intolerable side effects, and without substantially changing overall survival. A better understanding of mechanisms underlying IPF is likely to lead to improved therapies. The current paradigm proposes that repetitive alveolar epithelial injury from noxious stimuli in a genetically primed individual is followed by abnormal wound healing, including aberrant activity of extracellular matrix-secreting cells, with resultant tissue fibrosis and parenchymal damage. However, this may underplay the importance of the vascular contribution to fibrogenesis. The lungs receive 100% of the cardiac output, and vascular abnormalities in IPF include (a) heterogeneous vessel formation throughout fibrotic lung, including the development of abnormal dilated vessels and anastomoses; (b) abnormal spatially distributed populations of endothelial cells (ECs); (c) dysregulation of endothelial protective pathways such as prostacyclin signaling; and (d) an increased frequency of common vascular and metabolic comorbidities. Here, we propose that vascular and EC abnormalities are both causal and consequential in the pathobiology of IPF and that fuller evaluation of dysregulated pathways may lead to effective therapies and a cure for this devastating disease.
    MeSH term(s) Humans ; Endothelial Cells ; Cicatrix ; Idiopathic Pulmonary Fibrosis ; Drug-Related Side Effects and Adverse Reactions ; Epoprostenol
    Chemical Substances Epoprostenol (DCR9Z582X0)
    Language English
    Publishing date 2023-09-15
    Publishing country United States
    Document type Journal Article ; Review ; Research Support, Non-U.S. Gov't
    ZDB-ID 3067-3
    ISSN 1558-8238 ; 0021-9738
    ISSN (online) 1558-8238
    ISSN 0021-9738
    DOI 10.1172/JCI172058
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Defining a pathological role for the vasculature in the development of fibrosis and pulmonary hypertension in interstitial lung disease.

    George, Peter M / Mitchell, Jane A

    American journal of physiology. Lung cellular and molecular physiology

    2019  Volume 317, Issue 4, Page(s) L431–L433

    MeSH term(s) Chemokines ; Fibrosis ; Humans ; Hypertension, Pulmonary ; Hypoxia ; Lung Diseases, Interstitial ; Myeloid Cells ; Pulmonary Fibrosis
    Chemical Substances Chemokines
    Language English
    Publishing date 2019-08-21
    Publishing country United States
    Document type Editorial ; Comment
    ZDB-ID 1013184-x
    ISSN 1522-1504 ; 1040-0605
    ISSN (online) 1522-1504
    ISSN 1040-0605
    DOI 10.1152/ajplung.00330.2019
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: L-arginine supplementation protects against thrombosis and renal dysfunction in mice treated with the cyclooxygenase-2 inhibitor parecoxib.

    Vaja, Ricky / Lopes-Pires, Maria / Shala, Fisnik / Cypaite, Neringa / Vinokurova, Maria / Ferreira, Plinio / Mitchell, Jane A / Kirkby, Nicholas S

    Journal of thrombosis and haemostasis : JTH

    2024  

    Language English
    Publishing date 2024-03-20
    Publishing country England
    Document type Letter
    ZDB-ID 2112661-6
    ISSN 1538-7836 ; 1538-7933
    ISSN (online) 1538-7836
    ISSN 1538-7933
    DOI 10.1016/j.jtha.2024.03.006
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  4. Article ; Online: Eicosanoids, prostacyclin and cyclooxygenase in the cardiovascular system.

    Mitchell, Jane A / Kirkby, Nicholas S

    British journal of pharmacology

    2018  Volume 176, Issue 8, Page(s) 1038–1050

    Abstract: Eicosanoids represent a diverse family of lipid mediators with fundamental roles in physiology and disease. Within the eicosanoid superfamily are prostanoids, which are specifically derived from arachidonic acid by the enzyme cyclooxygenase (COX). COX ... ...

    Abstract Eicosanoids represent a diverse family of lipid mediators with fundamental roles in physiology and disease. Within the eicosanoid superfamily are prostanoids, which are specifically derived from arachidonic acid by the enzyme cyclooxygenase (COX). COX has two isoforms; COX-1 and COX-2. COX-2 is the therapeutic target for the nonsteroidal anti-inflammatory drug (NSAID) class of pain medications. Of the prostanoids, prostacyclin, first discovered by Sir John Vane in 1976, remains amongst the best studied and retains an impressive pedigree as one of the fundamental cardiovascular protective pathways. Since this time, we have learnt much about how eicosanoids, COX enzymes and prostacyclin function in the cardiovascular system, knowledge that has allowed us, for example, to harness the power of prostacyclin as therapy to treat pulmonary arterial hypertension and peripheral vascular disease. However, there remain many unanswered questions in our basic understanding of the pathways, and how they can be used to improve human health. Perhaps, the most important and controversial outstanding question in the field remains; 'how do NSAIDs produce their much publicized cardiovascular side-effects?' This review summarizes the history, biology and cardiovascular function of key eicosanoids with particular focus on prostacyclin and other COX products and discusses how our knowledge of these pathways can applied in future drug discovery and be used to explain the cardiovascular side-effects of NSAIDs. LINKED ARTICLES: This article is part of a themed section on Eicosanoids 35 years from the 1982 Nobel: where are we now? To view the other articles in this section visit http://onlinelibrary.wiley.com/doi/10.1111/bph.v176.8/issuetoc.
    MeSH term(s) Animals ; Anti-Inflammatory Agents, Non-Steroidal/adverse effects ; Cardiovascular Diseases/chemically induced ; Cardiovascular Diseases/metabolism ; Cardiovascular System/metabolism ; Cyclooxygenase 1/metabolism ; Cyclooxygenase 2/metabolism ; Eicosanoids/metabolism ; Epoprostenol/metabolism ; Humans
    Chemical Substances Anti-Inflammatory Agents, Non-Steroidal ; Eicosanoids ; Epoprostenol (DCR9Z582X0) ; Cyclooxygenase 1 (EC 1.14.99.1) ; Cyclooxygenase 2 (EC 1.14.99.1) ; PTGS1 protein, human (EC 1.14.99.1)
    Language English
    Publishing date 2018-04-14
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Review
    ZDB-ID 80081-8
    ISSN 1476-5381 ; 0007-1188
    ISSN (online) 1476-5381
    ISSN 0007-1188
    DOI 10.1111/bph.14167
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Pulmonary Hypertension-Associated Right Ventricular Cardiomyocyte Remodelling Reduces Treprostinil Function.

    Judina, Aleksandra / Niglas, Marili / Leonov, Vladislav / Kirkby, Nicholas S / Diakonov, Ivan / Wright, Peter T / Zhao, Lan / Mitchell, Jane A / Gorelik, Julia

    Cells

    2023  Volume 12, Issue 23

    Abstract: 1) Pulmonary hypertension (PH)-associated right ventricular (RV) failure is linked to a reduction in pulmonary vasodilators. Treprostinil has shown effectiveness in PAH patients with cardiac decompensation, hinting at potential cardiac benefits. We ... ...

    Abstract (1) Pulmonary hypertension (PH)-associated right ventricular (RV) failure is linked to a reduction in pulmonary vasodilators. Treprostinil has shown effectiveness in PAH patients with cardiac decompensation, hinting at potential cardiac benefits. We investigated treprostinil's synergy with isoprenaline in RV and LV cardiomyocytes. We hypothesised that disease-related RV structural changes in cardiomyocytes would reduce contractile responses and cAMP/PKA signalling activity. (2) We induced PH in male Sprague Dawley rats using monocrotaline and isolated their ventricular cardiomyocytes. The effect of in vitro treprostinil and isoprenaline stimulation on contraction was assessed. FRET microscopy was used to study PKA activity associated with treprostinil stimulation in AKAR3-NES FRET-based biosensor-expressing cells. (3) RV cells exhibited maladaptive remodelling with hypertrophy, impaired contractility, and calcium transients compared to control and LV cardiomyocytes. Combining treprostinil and isoprenaline failed to enhance inotropy in PH RV cardiomyocytes. PH RV cardiomyocytes displayed an aberrant contractile behaviour, which the combination treatment could not rectify. Finally, we observed decreased PKA activity in treprostinil-treated PH RV cardiomyocytes. (4) PH-associated RV cardiomyocyte remodelling reduced treprostinil sensitivity, inotropic support, and impaired relaxation. Overall, this study highlights the complexity of RV dysfunction in advanced PH and suggests the need for alternative therapeutic strategies.
    MeSH term(s) Humans ; Rats ; Animals ; Male ; Hypertension, Pulmonary ; Myocytes, Cardiac ; Isoproterenol/pharmacology ; Rats, Sprague-Dawley ; Heart Failure
    Chemical Substances treprostinil (RUM6K67ESG) ; Isoproterenol (L628TT009W)
    Language English
    Publishing date 2023-12-04
    Publishing country Switzerland
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2661518-6
    ISSN 2073-4409 ; 2073-4409
    ISSN (online) 2073-4409
    ISSN 2073-4409
    DOI 10.3390/cells12232764
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Oral nitrate supplementation improves cardiovascular risk markers in COPD: ON-BC, a randomised controlled trial.

    Alasmari, Ali M / Alsulayyim, Abdullah S / Alghamdi, Saeed M / Philip, Keir E J / Buttery, Sara C / Banya, Winston A S / Polkey, Michael I / Armstrong, Paul C / Rickman, Matthew J / Warner, Timothy D / Mitchell, Jane A / Hopkinson, Nicholas S

    The European respiratory journal

    2024  Volume 63, Issue 2

    Abstract: Background: Short-term studies suggest that dietary nitrate (NO: Methods: The ON-BC trial was a randomised, double-blind, placebo-controlled parallel group study in stable COPD patients with home systolic BP (SBP) measurement ≥130 mmHg. Participants ... ...

    Abstract Background: Short-term studies suggest that dietary nitrate (NO
    Methods: The ON-BC trial was a randomised, double-blind, placebo-controlled parallel group study in stable COPD patients with home systolic BP (SBP) measurement ≥130 mmHg. Participants were randomly allocated (1:1) using computer-generated, block randomisation to either 70 mL NR-BRJ (400 mg NO
    Results: Compared with placebo, active treatment lowered SBP (Hodges-Lehmann treatment effect -4.5 (95% CI -5.9- -3.0) mmHg), and improved 6MWD (30.0 (95% CI 15.7-44.2) m; p<0.001), RHI (0.34 (95% CI 0.03-0.63); p=0.03) and AIx75 (-7.61% (95% CI -14.3- -0.95%); p=0.026).
    Conclusions: In people with COPD, prolonged dietary nitrate supplementation in the form of beetroot juice produces a sustained reduction in BP, associated with an improvement in endothelial function and exercise capacity.
    MeSH term(s) Humans ; Nitrates/therapeutic use ; Cardiovascular Diseases/prevention & control ; Cardiovascular Diseases/drug therapy ; Dietary Supplements ; Risk Factors ; Blood Pressure ; Antioxidants ; Pulmonary Disease, Chronic Obstructive/complications ; Pulmonary Disease, Chronic Obstructive/drug therapy ; Double-Blind Method ; Cross-Over Studies
    Chemical Substances Nitrates ; Antioxidants
    Language English
    Publishing date 2024-02-01
    Publishing country England
    Document type Randomized Controlled Trial ; Journal Article
    ZDB-ID 639359-7
    ISSN 1399-3003 ; 0903-1936
    ISSN (online) 1399-3003
    ISSN 0903-1936
    DOI 10.1183/13993003.02353-2022
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  7. Article: PPARβ/δ a potential target in pulmonary hypertension blighted by cancer risk.

    Mitchell, Jane A / Bishop-Bailey, David

    Pulmonary circulation

    2018  Volume 9, Issue 1, Page(s) 2045894018812053

    Language English
    Publishing date 2018-10-23
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2638089-4
    ISSN 2045-8940 ; 2045-8932
    ISSN (online) 2045-8940
    ISSN 2045-8932
    DOI 10.1177/2045894018812053
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  8. Article ; Online: Imaging of Tissue-Specific and Temporal Activation of GPCR Signaling Using DREADD Knock-In Mice.

    Akhmedov, Dmitry / Kirkby, Nicholas S / Mitchell, Jane A / Berdeaux, Rebecca

    Methods in molecular biology (Clifton, N.J.)

    2019  Volume 1947, Page(s) 361–376

    Abstract: Engineered G protein-coupled receptors (DREADDs, designer receptors exclusively activated by designer drugs) are convenient tools for specific activation of GPCR signaling in many cell types. DREADDs have been utilized as research tools to study numerous ...

    Abstract Engineered G protein-coupled receptors (DREADDs, designer receptors exclusively activated by designer drugs) are convenient tools for specific activation of GPCR signaling in many cell types. DREADDs have been utilized as research tools to study numerous cellular and physiologic processes, including regulation of neuronal activity, behavior, and metabolism. Mice with random insertion transgenes and adeno-associated viruses have been widely used to express DREADDs in individual cell types. We recently created and characterized ROSA26-GsDREADD knock-in mice to allow Cre recombinase-dependent expression of a Gαs-coupled DREADD (GsD) fused to GFP in distinct cell populations in vivo. These animals also harbor a CREB-activated luciferase reporter gene for analysis of CREB activity by in vivo imaging, ex vivo imaging, or biochemical reporter assays. In this chapter, we provide detailed methods for breeding GsD animals, inducing GsD expression, stimulating GsD activity, and measuring basal and stimulated CREB reporter bioluminescence in tissues in vivo, ex vivo, and in vitro. These animals are available from our laboratory for non-profit research.
    MeSH term(s) Animals ; Clozapine/analogs & derivatives ; Clozapine/pharmacology ; Cyclic AMP/metabolism ; Cyclic AMP Response Element-Binding Protein/metabolism ; Genes, Reporter ; Image Processing, Computer-Assisted/methods ; Integrases/metabolism ; Luminescent Measurements/methods ; Membrane Transport Modulators/pharmacology ; Mice ; Organ Specificity ; Receptors, G-Protein-Coupled/drug effects ; Receptors, G-Protein-Coupled/genetics ; Receptors, G-Protein-Coupled/metabolism ; Signal Transduction
    Chemical Substances Creb1 protein, mouse ; Cyclic AMP Response Element-Binding Protein ; Membrane Transport Modulators ; Receptors, G-Protein-Coupled ; Cyclic AMP (E0399OZS9N) ; Integrases (EC 2.7.7.-) ; Clozapine (J60AR2IKIC) ; clozapine N-oxide (MZA8BK588J)
    Language English
    Publishing date 2019-04-09
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ISSN 1940-6029
    ISSN (online) 1940-6029
    DOI 10.1007/978-1-4939-9121-1_21
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Evidence that pulmonary vascular pathology explains the decline in lung function associated with interferon α based therapies for chronic hepatitis C virus.

    George, Peter M / Mitchell, Jane A

    Journal of viral hepatitis

    2013  Volume 20, Issue 8, Page(s) 592

    MeSH term(s) Albumins/adverse effects ; Antiviral Agents/adverse effects ; Female ; Hepatitis C, Chronic/drug therapy ; Humans ; Interferon-alpha/adverse effects ; Lung/drug effects ; Lung Diseases, Interstitial/chemically induced ; Male ; Polyethylene Glycols/adverse effects ; Ribavirin/adverse effects
    Chemical Substances Albumins ; Antiviral Agents ; Interferon-alpha ; Polyethylene Glycols (3WJQ0SDW1A) ; Ribavirin (49717AWG6K)
    Language English
    Publishing date 2013-07-15
    Publishing country England
    Document type Letter ; Comment
    ZDB-ID 1212497-7
    ISSN 1365-2893 ; 1352-0504
    ISSN (online) 1365-2893
    ISSN 1352-0504
    DOI 10.1111/jvh.12105
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  10. Article ; Online: Reply to Ricciotti et al.: Evidence for vascular COX isoforms.

    Mitchell, Jane A / Warner, Timothy D

    Proceedings of the National Academy of Sciences of the United States of America

    2013  Volume 110, Issue 3, Page(s) E184

    MeSH term(s) Animals ; Cardiovascular System/metabolism ; Cyclooxygenase 1/metabolism ; Cyclooxygenase 2/metabolism ; Epoprostenol/biosynthesis ; Humans
    Chemical Substances Epoprostenol (DCR9Z582X0) ; Cyclooxygenase 1 (EC 1.14.99.1) ; Cyclooxygenase 2 (EC 1.14.99.1)
    Language English
    Publishing date 2013-02-05
    Publishing country United States
    Document type Letter ; Comment
    ZDB-ID 209104-5
    ISSN 1091-6490 ; 0027-8424
    ISSN (online) 1091-6490
    ISSN 0027-8424
    DOI 10.1073/pnas.1219532110
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