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U radu daje se detaljan pregled najvažnijih osoba i događaja koji su obilježili razdoblje vladavine dinastije Karolinga u razdoblju ranoga europskoga srednjovjekovlja, naslijedivši dinastiju Merovinga u Franačkoj, učvrstivši svoju vlast u Franačkoj krajem 7. stoljeća. Dva najvažnija vladara, Pipin Mali i Karlo Veliki, predstavljaju važne povijesne osobe koje su svojim djelovanjem obilježili europsku povijest. Svojim djelovanjem spojili su svjetovnu i crkvenu vlast sklapajući sporazume s mnogim tadašnjim papama. Vrhunac franačke države i karolinške dinastije ipak predstavlja razdoblje vladavine monarha Karla Velikog, koja uglavnom obuhvaća razdoblje od 771. do 814. godine, od samostalnog preuzimanja prijestolja pa sve do smrti. Svojom je vladavinom omogućio razvoj u vanjskopolitičkom i unutarnjopolitičkom planu. Vodeći većinom uspješne i mnogobrojne ratove, proširio je znatno opseg države, a dodatnu čvrstoću stekao je savezništvom sa Svetom Stolicom. S druge strane, kulturnim i društvenim reformama postigao je određenu stabilnost unutar same države. U njegovo doba dolazi i do kulturnog procvata poznatog pod nazivom karolinška renesansa koji ujedno i označava prvi značajni razvoj kulture tijekom srednjeg vijeka u Europi nakon razdoblja duge kulturne stagnacije. Karlovom smrću dolazi do raspada državnog jedinstva podjelom države na tri dijela 843. godine Verdunskim sporazumom

Innate Cytokine Induced Early Release of IFNγ and CC Chemokines from Hypoxic Human NK Cells Is Independent of Glucose

Natural killer (NK) cells are among the first innate immune cells to arrive at sites of tissue inflammation and regulate the immune response to infection and tumors by the release of cytokines including interferon (IFN)γ. In vitro exposure to the innate cytokines interleukin 15 (IL-15) and IL-12/IL-18 enhances NK cell IFNγ production which, beyond 16 h of culture, was shown to depend on metabolic switching to glycolysis. NK effector responses are, however, rapid by comparison. Therefore, we sought to evaluate the importance of glycolysis for shorter-term IFNγ production, considering glucose deprivation and hypoxia as adverse tissue inflammation associated conditions. Treatments with IL-15 for 6 and 16 h were equally effective in priming early IFNγ production in human NK cells in response to secondary IL-12/IL-18 stimulation. Short-term priming was not associated with glycolytic switching but induced the release of IFNγ and, additionally, CCL3, CCL4 and CCL5 from both normoxic and hypoxic NK cells in an equally efficient and, unexpectedly, glucose independent manner. We conclude that release of IFNγ and CC chemokines in the early innate immune response is a metabolically autonomous NK effector program

S-Adenosylhomocysteine Is a Useful Metabolic Factor in the Early Prediction of Septic Disease Progression and Death in Critically Ill Patients: A Prospective Cohort Study

A common final pathway of pathogenetic mechanisms in septic organ dysfunction and death is a lack or non-utilization of oxygen. Plasma concentrations of lactate serve as surrogates for the oxygen-deficiency-induced imbalance between energy supply and demand. As S-adenosylhomocysteine (SAH) was shown to reflect tissue hypoxia, we compared the ability of SAH versus lactate to predict the progression of inflammatory and septic disease to septic organ dysfunction and death. Using univariate and multiple logistic regression, we found that SAH but not lactate, taken upon patients’ inclusion in the study close to ICU admission, significantly and independently contributed to the prediction of disease progression and death. Due to the stronger increase in SAH in relation to S-adenosylmethionine (SAM), the ratio of SAM to SAH, representing methylation potential, was significantly decreased in patients with septic organ dysfunction and non-survivors compared with SIRS/sepsis patients (2.8 (IQR 2.3–3.9) vs. 8.8 (4.9–13.8); p = 0.003) or survivors (4.9 (2.8–9.5) vs. 8.9 (5.1–14.3); p = 0.026), respectively. Thus, SAH appears to be a better contributor to the prediction of septic organ dysfunction and death than lactate in critically ill patients. As SAH is a potent inhibitor of SAM-dependent methyltransferases involved in numerous vital biochemical processes, the impairment of the SAM-to-SAH ratio in severely critically ill septic patients and non-survivors warrants further studies on the pathogenetic role of SAH in septic multiple organ failure