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1h-(1,2,4)oxadiazolo(4,3-a)quinoxalin-1-one and Sepsis

1h-(1,2,4)oxadiazolo(4,3-a)quinoxalin-1-one has been researched along with Sepsis in 8 studies

1H-(1,2,4)oxadiazolo(4,3-a)quinoxalin-1-one: structure given in first source; inhibits guanylyl cyclase
1H-[1,2,4]oxadiazolo[4,3-a]quinoxalin-1-one : A member of the class of oxadiazoloquinoxalines that is 1H-[1,2,4]oxadiazolo[4,3-a]quinoxaline substituted at position 1 by an oxo group.

Sepsis: Systemic inflammatory response syndrome with a proven or suspected infectious etiology. When sepsis is associated with organ dysfunction distant from the site of infection, it is called severe sepsis. When sepsis is accompanied by HYPOTENSION despite adequate fluid infusion, it is called SEPTIC SHOCK.

Research Excerpts

ExcerptRelevanceReference
"Atorvastatin pretreatment, however, prevented the decrease in α(1D)-adrenoceptor mRNA expression in septic animals."5.37Atorvastatin prevents vascular hyporeactivity to norepinephrine in sepsis: role of nitric oxide and α₁-adrenoceptor mRNA expression. ( Ahanger, AA; Choudhury, S; Kandasamy, K; Mishra, SK; More, AS; Parida, S; Prawez, S; Singh, TU, 2011)
" In a phenylephrine-contracted canine carotid artery ring preparation, we found that both canine and human Lzm-S, at concentrations similar to those found in sepsis, produced vasorelaxation."3.74Lysozyme, a mediator of sepsis that produces vasodilation by hydrogen peroxide signaling in an arterial preparation. ( Bose, R; Cheng, ZQ; Jacobs, H; Kasian, K; Light, RB; Mink, SN; Santos Martinez, LE, 2008)
"Sepsis was induced by cecal ligation and puncture (CLP)."1.56Perivascular adipose tissue phenotype and sepsis vascular dysfunction: Differential contribution of NO, ROS and beta 3-adrenergic receptor. ( Assreuy, J; Barp, CG; Benedet, PO, 2020)
"Atorvastatin pretreatment, however, prevented the decrease in α(1D)-adrenoceptor mRNA expression in septic animals."1.37Atorvastatin prevents vascular hyporeactivity to norepinephrine in sepsis: role of nitric oxide and α₁-adrenoceptor mRNA expression. ( Ahanger, AA; Choudhury, S; Kandasamy, K; Mishra, SK; More, AS; Parida, S; Prawez, S; Singh, TU, 2011)

Research

Studies (8)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's5 (62.50)29.6817
2010's2 (25.00)24.3611
2020's1 (12.50)2.80

Authors

AuthorsStudies
Barp, CG1
Benedet, PO1
Assreuy, J2
Fernandes, D1
Sordi, R1
Pacheco, LK1
Nardi, GM1
Heckert, BT1
Villela, CG1
Lobo, AR1
Barja-Fidalgo, C1
Oliveira-Pelegrin, GR1
Aguila, FA1
Basso, PJ1
Rocha, MJ1
Kandasamy, K1
Prawez, S1
Choudhury, S1
More, AS1
Ahanger, AA1
Singh, TU1
Parida, S1
Mishra, SK1
Williams, M1
Kerkar, S1
Tyburski, JG1
Steffes, CP1
Carlin, AM1
Wilson, RF1
Wang, C1
Mansard, A1
Giummelly, P1
Atkinson, J1
Mink, SN2
Bose, R2
Roberts, DE1
Jacobs, H2
Duke, K1
Bose, D1
Cheng, ZQ2
Light, RB2
Kasian, K1
Santos Martinez, LE1

Other Studies

8 other studies available for 1h-(1,2,4)oxadiazolo(4,3-a)quinoxalin-1-one and Sepsis

ArticleYear
Perivascular adipose tissue phenotype and sepsis vascular dysfunction: Differential contribution of NO, ROS and beta 3-adrenergic receptor.
    Life sciences, 2020, Aug-01, Volume: 254

    Topics: Acetophenones; Adipose Tissue; Adrenergic beta-3 Receptor Agonists; Animals; Aorta; Cyclic N-Oxides;

2020
Late, but not early, inhibition of soluble guanylate cyclase decreases mortality in a rat sepsis model.
    The Journal of pharmacology and experimental therapeutics, 2009, Volume: 328, Issue:3

    Topics: Animals; Aorta, Thoracic; Blood Pressure; Cecum; Cyclic GMP; Disease Models, Animal; Drug Administra

2009
Role of central NO-cGMP pathway in vasopressin and oxytocin gene expression during sepsis.
    Peptides, 2010, Volume: 31, Issue:10

    Topics: Animals; Arginine Vasopressin; Cyclic GMP; Enzyme Inhibitors; Gene Expression Regulation; Male; Nitr

2010
Atorvastatin prevents vascular hyporeactivity to norepinephrine in sepsis: role of nitric oxide and α₁-adrenoceptor mRNA expression.
    Shock (Augusta, Ga.), 2011, Volume: 36, Issue:1

    Topics: Animals; Atorvastatin; Enzyme Inhibitors; Guanylate Cyclase; Heptanoic Acids; Mice; Nitric Oxide; No

2011
The roles of cyclic adenosine monophosphate- and cyclic guanosine monophosphate-dependent protein kinase pathways in hydrogen peroxide-induced contractility of microvascular lung pericytes.
    The Journal of trauma, 2003, Volume: 55, Issue:4

    Topics: Adenine; Adenylyl Cyclase Inhibitors; Analysis of Variance; Animals; Cell Survival; Cells, Cultured;

2003
Decreased aortic smooth muscle contraction in a rat model of multibacterial sepsis.
    Fundamental & clinical pharmacology, 2004, Volume: 18, Issue:6

    Topics: Animals; Aorta; Disease Models, Animal; Endothelial Cells; Enzyme Inhibitors; Guanylate Cyclase; In

2004
Lysozyme binding to endocardial endothelium mediates myocardial depression by the nitric oxide guanosine 3',5' monophosphate pathway in sepsis.
    Journal of molecular and cellular cardiology, 2005, Volume: 39, Issue:4

    Topics: Animals; Cell Membrane; Cyclic GMP; Dogs; Endocardium; Endothelium; In Vitro Techniques; Muramidase;

2005
Lysozyme, a mediator of sepsis that produces vasodilation by hydrogen peroxide signaling in an arterial preparation.
    American journal of physiology. Heart and circulatory physiology, 2008, Volume: 294, Issue:4

    Topics: Aminoquinolines; Animals; Carotid Artery, Internal; Catalase; Cyclic GMP; Cyclic GMP-Dependent Prote

2008