2007
DOI: 10.1001/jama.297.15.joc70035
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Effect of Tilarginine Acetate in Patients With Acute Myocardial Infarction and Cardiogenic Shock

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Cited by 335 publications
(97 citation statements)
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References 22 publications
(44 reference statements)
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“…I had proposed a slightly extended Warburg effect which I would 38 like to call it as 'Warburg common pathogenesis model or Warburg differentiation dedifferentiation 39 effect', which has the potential to explain septic shock and sepsis associated multi-organ dysfunction 40 and many other major pathologies like SHT, PAH, CHF, DM, Asthma, ARDS, AKI implying most 41 of the diseases may have a common pathogenesis as the underlying mechanism. 42 Increased Nitric oxide (NO) in sepsis via iNOS or any respiratory poison in general irreversibly 43 inhibits the mitochondrial respiration and shifts the metabolic phenotype of the cell from oxidative 44 phosphorylation (OXPHOS) to glycolytic phenotype and the change in metabolic phenotype is 45 followed by the change in cell phenotype from the normal adult dynamic differentiation state to 46 irreversible dedifferentiation states -embryonic phenotype, synthetic / proliferative phenotype, and 47 cancer phenotype. This dedifferentiated state switching can be seen as the cells local survival 48 strategy in response to injuries, but returning to their primitive forms leads to disorder and ends in 49 global collapse of the organ systems and organism which requires order in terms of differentiation.…”
Section: Abstract: 36mentioning
confidence: 99%
See 1 more Smart Citation
“…I had proposed a slightly extended Warburg effect which I would 38 like to call it as 'Warburg common pathogenesis model or Warburg differentiation dedifferentiation 39 effect', which has the potential to explain septic shock and sepsis associated multi-organ dysfunction 40 and many other major pathologies like SHT, PAH, CHF, DM, Asthma, ARDS, AKI implying most 41 of the diseases may have a common pathogenesis as the underlying mechanism. 42 Increased Nitric oxide (NO) in sepsis via iNOS or any respiratory poison in general irreversibly 43 inhibits the mitochondrial respiration and shifts the metabolic phenotype of the cell from oxidative 44 phosphorylation (OXPHOS) to glycolytic phenotype and the change in metabolic phenotype is 45 followed by the change in cell phenotype from the normal adult dynamic differentiation state to 46 irreversible dedifferentiation states -embryonic phenotype, synthetic / proliferative phenotype, and 47 cancer phenotype. This dedifferentiated state switching can be seen as the cells local survival 48 strategy in response to injuries, but returning to their primitive forms leads to disorder and ends in 49 global collapse of the organ systems and organism which requires order in terms of differentiation.…”
Section: Abstract: 36mentioning
confidence: 99%
“…198 Nitric oxide role in septic shock is an extensively researched area, reviewed in (43,44). An early 199 hypotension and late hypotension has been already shown in sepsis, initial phase is considered to be 200 due to increased eNOS activity and late hypotension is considered to be due to iNOS action (41, 201 42).Inhibition of iNOS has been tried as a treatment option for shock ,eventhough NOS inhibitors 202 were successful in animal studies, TRIUMPH trial conducted using nonspecific NOS inhibitor 203 tilarginine in cardiogenic shock in humans didn't showed beneficial effect, also it showed it may be 204 harmful (45). Many thought the reason for failure may be due to the nonspecific inhibition of NOS 205 and selective iNOS inhibition with eNOS restoration may be beneficial (46,47).…”
Section: Warburg Common Pathogenesis Model In Sepsis (Figure 2): 173mentioning
confidence: 99%
“…However, with advances in coronary reperfusion techniques over the past few decades, especially with the introduction of primary percutaneous percutaneous coronary intervention, the mortality rate has improved to below 50% 4,[6][7][8][9][10][11][12] . The trend toward better outcomes may also be due to greatly awareness of the need for timely treatment, improvements in the medical care of haemodynamically unstable patients as well as the use of mechanical support devices, though this has not yet been clearly demonstrated.…”
Section: Incidence and Prognosis Of Cardiogenic Shockmentioning
confidence: 99%
“…5 However, with advances in coronary reperfusion techniques over the past few decades, especially with the introduction of primary percutaneous coronary intervention (PCI), the mortality rate has improved to below 50 %. 4,[6][7][8][9][10][11][12] The trend towards better outcomes may also be due to greater awareness of the need for timely treatment, improvements in the medical care of haemodynamically unstable patients as well as the use of mechanical support devices, although this has not yet been clearly demonstrated.Despite this high mortality rate, it is important to note that patients with cardiogenic shock who survive to discharge have a long-term outcome similar to that of patients without cardiogenic shock, with a good functional outcome at 1 year. 13,14 This highlights the importance of improving the chance of early survival among patients in cardiogenic shock.…”
mentioning
confidence: 99%