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  1. Article: The immunomodulatory role of IDO1-Kynurenine-NAD

    Anu, R I / Shiu, Kai-Keen / Khan, Khurum Hayat

    Frontiers in oncology

    2023  Volume 13, Page(s) 1142838

    Abstract: ... concentration of NAD and is upregulated in the tumor. In light of the potential role of IDO1 as a driver ... of hostile TME in PDAC and NAD ...

    Abstract Pancreatic ductal adenocarcinoma (PDAC) is the most common exocrine tumor of the pancreas characterized by late diagnosis, adverse overall 5-year survival, a higher propensity for metastatic disease, and lack of efficacy of systemic therapy options. These adverse outcomes can be partly attributed to complex tumor microenvironment (TME). Over the past decade, immunotherapy has revolutionized the management of certain cancers; thus far, the immunologically 'non-inflamed' tumor microenvironment in PDACs has proven to be challenging. Indolamine 2,3-dioxygenase 1 (IDO1) is the rate-limiting enzyme in the catabolic pathway of L-Tryptophan, an essential amino acid, that gives rise to the immunosuppressive metabolite Kynurenine. IDO1, Indolamine 2,3-dioxygenase 2 (IDO2), and Tryptophan 2,3-dioxygenase (TDO) are the key enzymes in the tryptophan catabolic pathway but we focus on the role of the predominant enzyme form IDO1 in this review. Nicotinamide phosphoribosyl transferase (iNAMPT) regulates the intracellular concentration of NAD and is upregulated in the tumor. In light of the potential role of IDO1 as a driver of hostile TME in PDAC and NAD
    Language English
    Publishing date 2023-06-30
    Publishing country Switzerland
    Document type Journal Article ; Review
    ZDB-ID 2649216-7
    ISSN 2234-943X
    ISSN 2234-943X
    DOI 10.3389/fonc.2023.1142838
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Dihydronicotinamide Riboside Is a Potent NAD

    Chini, Claudia C S / Peclat, Thais R / Gomez, Lilian S / Zeidler, Julianna D / Warner, Gina M / Kashyap, Sonu / Mazdeh, Delaram Z / Hayat, Faisal / Migaud, Marie E / Paulus, Aneel / Chanan-Khan, Asher A / Chini, Eduardo N

    Frontiers in immunology

    2022  Volume 13, Page(s) 840246

    Abstract: Nicotinamide adenine dinucleotide (NAD) metabolism plays an important role in the regulation ... of immune function. However, a complete picture of how NAD, its metabolites, precursors, and metabolizing ... functions. Therefore, we investigated the role of NAD boosting in the regulation of macrophage activation ...

    Abstract Nicotinamide adenine dinucleotide (NAD) metabolism plays an important role in the regulation of immune function. However, a complete picture of how NAD, its metabolites, precursors, and metabolizing enzymes work together in regulating immune function and inflammatory diseases is still not fully understood. Surprisingly, few studies have compared the effect of different forms of vitamin B3 on cellular functions. Therefore, we investigated the role of NAD boosting in the regulation of macrophage activation and function using different NAD precursors supplementation. We compared nicotinamide mononucleotide (NMN), nicotinamide riboside (NR), and nicotinamide (NAM) supplementation, with the recently described potent NAD precursor NRH. Our results show that only NRH supplementation strongly increased NAD
    MeSH term(s) Cytokines ; Glycosides ; Macrophages/metabolism ; NAD/metabolism ; Niacinamide/analogs & derivatives ; Niacinamide/pharmacology ; Phenotype
    Chemical Substances Cytokines ; Glycosides ; dihydronicotinamide ; NAD (0U46U6E8UK) ; Niacinamide (25X51I8RD4)
    Language English
    Publishing date 2022-02-25
    Publishing country Switzerland
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 2606827-8
    ISSN 1664-3224 ; 1664-3224
    ISSN (online) 1664-3224
    ISSN 1664-3224
    DOI 10.3389/fimmu.2022.840246
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Boosting NAD

    Gardell, Stephen J / Hopf, Meghan / Khan, Asima / Dispagna, Mauro / Hampton Sessions, E / Falter, Rebecca / Kapoor, Nidhi / Brooks, Jeanne / Culver, Jeffrey / Petucci, Chris / Ma, Chen-Ting / Cohen, Steven E / Tanaka, Jun / Burgos, Emmanuel S / Hirschi, Jennifer S / Smith, Steven R / Sergienko, Eduard / Pinkerton, Anthony B

    Nature communications

    2019  Volume 10, Issue 1, Page(s) 3241

    Abstract: Pharmacological strategies that boost intracellular NAD ...

    Abstract Pharmacological strategies that boost intracellular NAD
    MeSH term(s) A549 Cells ; Animals ; Biocatalysis/drug effects ; Enzyme Activators/administration & dosage ; Enzyme Activators/chemistry ; Enzyme Activators/pharmacology ; Humans ; Intracellular Space/drug effects ; Intracellular Space/metabolism ; Liver/drug effects ; Liver/metabolism ; Mice ; Molecular Structure ; NAD/metabolism ; Nicotinamide Mononucleotide/metabolism ; Nicotinamide Phosphoribosyltransferase/metabolism ; Phosphorylation/drug effects ; Small Molecule Libraries/administration & dosage ; Small Molecule Libraries/chemistry ; Small Molecule Libraries/pharmacology
    Chemical Substances Enzyme Activators ; Small Molecule Libraries ; NAD (0U46U6E8UK) ; Nicotinamide Mononucleotide (1094-61-7) ; Nicotinamide Phosphoribosyltransferase (EC 2.4.2.12)
    Language English
    Publishing date 2019-07-19
    Publishing country England
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't ; Research Support, U.S. Gov't, Non-P.H.S.
    ZDB-ID 2553671-0
    ISSN 2041-1723 ; 2041-1723
    ISSN (online) 2041-1723
    ISSN 2041-1723
    DOI 10.1038/s41467-019-11078-z
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Niacin Cures Systemic NAD

    Pirinen, Eija / Auranen, Mari / Khan, Nahid A / Brilhante, Virginia / Urho, Niina / Pessia, Alberto / Hakkarainen, Antti / Kuula, Juho / Heinonen, Ulla / Schmidt, Mark S / Haimilahti, Kimmo / Piirilä, Päivi / Lundbom, Nina / Taskinen, Marja-Riitta / Brenner, Charles / Velagapudi, Vidya / Pietiläinen, Kirsi H / Suomalainen, Anu

    Cell metabolism

    2020  Volume 31, Issue 6, Page(s) 1078–1090.e5

    Abstract: NAD ...

    Abstract NAD
    MeSH term(s) Adolescent ; Adult ; Aged ; Female ; Humans ; Male ; Middle Aged ; Mitochondrial Myopathies/metabolism ; Mitochondrial Myopathies/pathology ; Muscles/metabolism ; Muscles/pathology ; NAD/deficiency ; NAD/metabolism ; Niacin/metabolism ; Young Adult
    Chemical Substances NAD (0U46U6E8UK) ; Niacin (2679MF687A)
    Language English
    Publishing date 2020-05-07
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2176834-1
    ISSN 1932-7420 ; 1550-4131
    ISSN (online) 1932-7420
    ISSN 1550-4131
    DOI 10.1016/j.cmet.2020.04.008
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Niacin Cures Systemic NAD

    Pirinen, Eija / Auranen, Mari / Khan, Nahid A / Brilhante, Virginia / Urho, Niina / Pessia, Alberto / Hakkarainen, Antti / Ulla Heinonen, Juho Kuula / Schmidt, Mark S / Haimilahti, Kimmo / Piirilä, Päivi / Lundbom, Nina / Taskinen, Marja-Riitta / Brenner, Charles / Velagapudi, Vidya / Pietiläinen, Kirsi H / Suomalainen, Anu

    Cell metabolism

    2020  Volume 32, Issue 1, Page(s) 144

    Language English
    Publishing date 2020-07-07
    Publishing country United States
    Document type Published Erratum
    ZDB-ID 2176834-1
    ISSN 1932-7420 ; 1550-4131
    ISSN (online) 1932-7420
    ISSN 1550-4131
    DOI 10.1016/j.cmet.2020.05.020
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: BMAL1 drives muscle repair through control of hypoxic NAD

    Zhu, Pei / Hamlish, Noah X / Thakkar, Abhishek Vijay / Steffeck, Adam W T / Rendleman, Emily J / Khan, Nabiha H / Waldeck, Nathan J / DeVilbiss, Andrew W / Martin-Sandoval, Misty S / Mathews, Thomas P / Chandel, Navdeep S / Peek, Clara B

    Genes & development

    2022  Volume 36, Issue 3-4, Page(s) 149–166

    Abstract: The process of tissue regeneration occurs in a developmentally timed manner, yet the role of circadian timing is not understood. Here, we identify a role for the adult muscle stem cell (MuSC)-autonomous clock in the control of muscle regeneration ... ...

    Abstract The process of tissue regeneration occurs in a developmentally timed manner, yet the role of circadian timing is not understood. Here, we identify a role for the adult muscle stem cell (MuSC)-autonomous clock in the control of muscle regeneration following acute ischemic injury. We observed greater muscle repair capacity following injury during the active/wake period as compared with the inactive/rest period in mice, and loss of
    MeSH term(s) ARNTL Transcription Factors/genetics ; Animals ; Cell Differentiation/genetics ; Hypoxia ; Mice ; Muscle Development/genetics ; Muscle, Skeletal ; Myoblasts ; NAD ; Satellite Cells, Skeletal Muscle
    Chemical Substances ARNTL Transcription Factors ; Bmal1 protein, mouse ; NAD (0U46U6E8UK)
    Language English
    Publishing date 2022-02-03
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural
    ZDB-ID 806684-x
    ISSN 1549-5477 ; 0890-9369
    ISSN (online) 1549-5477
    ISSN 0890-9369
    DOI 10.1101/gad.349066.121
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Meta-analysis of NAD(P)(H) quantification results exhibits variability across mammalian tissues.

    Azouaoui, Dassine / Choinière, Michael René / Khan, Momtafin / Sayfi, Shahab / Jaffer, Simran / Yousef, Selvia / Patten, David A / Green, Alexander E / Menzies, Keir J

    Scientific reports

    2023  Volume 13, Issue 1, Page(s) 2464

    Abstract: Nicotinamide Adenine Dinucleotide (NAD ...

    Abstract Nicotinamide Adenine Dinucleotide (NAD
    MeSH term(s) Humans ; Rats ; Mice ; Animals ; NAD/metabolism ; Energy Metabolism ; Mammals/metabolism
    Chemical Substances NAD (0U46U6E8UK)
    Language English
    Publishing date 2023-02-11
    Publishing country England
    Document type Meta-Analysis ; Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2615211-3
    ISSN 2045-2322 ; 2045-2322
    ISSN (online) 2045-2322
    ISSN 2045-2322
    DOI 10.1038/s41598-023-29607-8
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Current And Emerging Trends In The Management Of Pyoderma Gangrenosum: A Literature Review.

    Muhammad, Sobia Wali / Hassan, Nadia / Khan, Samra / Gohar, Atia

    Journal of Ayub Medical College, Abbottabad : JAMC

    2024  Volume 35Suppl 1, Issue 4, Page(s) S774–S784

    Abstract: The first description of Pyoderma gangrenosum (PG) was made about a century ago. It is difficult to understand the aetiology, pathophysiology, and therapy of PG. This disease is believed to be caused by a systemic inflammatory response to neutrophil ... ...

    Abstract The first description of Pyoderma gangrenosum (PG) was made about a century ago. It is difficult to understand the aetiology, pathophysiology, and therapy of PG. This disease is believed to be caused by a systemic inflammatory response to neutrophil chemotaxis and faulty innate immune system control. Nearly fifty percent of the cases have underlying systemic symptoms. Significant improvements in PG management have been made over the years. The main goals of treatment are to reduce inflammation and speed up the healing of the PG wound. Even though the most recent medicines show promise, they are found on isolated case reports. The majority of patients are typically managed with topical treatment and local wound care, while resistant cases necessitate immunosuppressive medications. More progress can be made with improvements in technology in deciphering this complex disease and getting a greater understanding of the condition. The present standard therapies for refractory PG are not well supported by studies. In refractory PG, corticosteroids and cyclosporine have historically been administered. Tumour necrosis factor inhibitors are becoming a viable option; nonetheless, this requires careful research and upkeep. This review intended to describe the current trends in managing the PG. Several next-generation treatment options including the conventional therapies introduced to treat PG. We encompass the advantages and disadvantages of new treatments for PG.
    MeSH term(s) Humans ; Pyoderma Gangrenosum/drug therapy ; Pyoderma Gangrenosum/diagnosis ; Inflammation/complications ; Inflammation/drug therapy ; Administration, Topical
    Language English
    Publishing date 2024-02-26
    Publishing country Pakistan
    Document type Review ; Journal Article
    ZDB-ID 2192473-9
    ISSN 1819-2718 ; 1025-9589
    ISSN (online) 1819-2718
    ISSN 1025-9589
    DOI 10.55519/JAMC-S4-12085
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Meta-analysis of NAD(P)(H) quantification results exhibits variability across mammalian tissues

    Dassine Azouaoui / Michael René Choinière / Momtafin Khan / Shahab Sayfi / Simran Jaffer / Selvia Yousef / David A. Patten / Alexander E. Green / Keir J. Menzies

    Scientific Reports, Vol 13, Iss 1, Pp 1-

    2023  Volume 13

    Abstract: Abstract Nicotinamide Adenine Dinucleotide (NAD+) plays an important role in energy metabolism and ... signaling pathways controlling crucial cellular functions. The increased interest in NAD+ metabolism and NAD+ ... boosting therapies has reinforced the necessity for accurate NAD+ quantification. To examine the published ...

    Abstract Abstract Nicotinamide Adenine Dinucleotide (NAD+) plays an important role in energy metabolism and signaling pathways controlling crucial cellular functions. The increased interest in NAD+ metabolism and NAD+-boosting therapies has reinforced the necessity for accurate NAD+ quantification. To examine the published NAD(P)(H) measures across mammalian tissues, we performed a meta-analysis of the existing data. An Ovid MEDLINE database search identified articles with NAD(P)(H) quantification results obtained from mammalian tissues published between 1961 and 2021. We screened 4890 records and extracted quantitative data, as well as the quantification methods, pre-analytical conditions, and subject characteristics. The extracted physiological NAD(P)(H) concentrations in various tissues from mice, rats, and humans, revealed an important inter- and intra-method variability that extended to recent publications. This highlights the relatively poor potential for cross-experimental analyses for NAD(P)(H) quantitative data and the importance of standardization for NAD(P)(H) quantification methods and pre-analytical procedures for future preclinical and clinical studies.
    Keywords Medicine ; R ; Science ; Q
    Subject code 001
    Language English
    Publishing date 2023-02-01T00:00:00Z
    Publisher Nature Portfolio
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  10. Article ; Online: Potential Modulation of Human NAD[P]H-Quinone Oxidoreductase 1 (NQO1) by EGCG and Its Metabolites-A Systematic Computational Study.

    Pandey, Pankaj / Avula, Bharathi / Khan, Ikhlas A / Khan, Shabana I / Navarro, Victor J / Doerksen, Robert J / Chittiboyina, Amar G

    Chemical research in toxicology

    2020  Volume 33, Issue 11, Page(s) 2749–2764

    Abstract: At high doses, green tea extracts and green tea's major active constituent, (-)-epigallocatechin gallate (EGCG), despite their generally perceived health benefits, have been suspected to cause hepatotoxicity in certain human populations. It has been ... ...

    Abstract At high doses, green tea extracts and green tea's major active constituent, (-)-epigallocatechin gallate (EGCG), despite their generally perceived health benefits, have been suspected to cause hepatotoxicity in certain human populations. It has been reported that
    MeSH term(s) Catechin/analogs & derivatives ; Catechin/chemistry ; Catechin/metabolism ; Catechin/pharmacology ; Humans ; Models, Molecular ; Molecular Structure ; NAD(P)H Dehydrogenase (Quinone)/antagonists & inhibitors ; NAD(P)H Dehydrogenase (Quinone)/chemistry ; NAD(P)H Dehydrogenase (Quinone)/metabolism ; Thermodynamics
    Chemical Substances Catechin (8R1V1STN48) ; epigallocatechin gallate (BQM438CTEL) ; NAD(P)H Dehydrogenase (Quinone) (EC 1.6.5.2) ; NQO1 protein, human (EC 1.6.5.2)
    Language English
    Publishing date 2020-11-02
    Publishing country United States
    Document type Journal Article ; Research Support, U.S. Gov't, Non-P.H.S.
    ZDB-ID 639353-6
    ISSN 1520-5010 ; 0893-228X
    ISSN (online) 1520-5010
    ISSN 0893-228X
    DOI 10.1021/acs.chemrestox.9b00450
    Database MEDical Literature Analysis and Retrieval System OnLINE

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