82 research outputs found
Microsecond Time-Resolved Absorption Spectroscopy Used to Study CO Compounds of Cytochrome bd from Escherichia coli
Cytochrome bd is a tri-heme (b558, b595, d) respiratory oxygen reductase that is found in many bacteria including pathogenic
species. It couples the electron transfer from quinol to O2 with generation of an electrochemical proton gradient. We
examined photolysis and subsequent recombination of CO with isolated cytochrome bd from Escherichia coli in oneelectron
reduced (MV) and fully reduced (R) states by microsecond time-resolved absorption spectroscopy at 532-nm
excitation. Both Soret and visible band regions were examined. CO photodissociation from MV enzyme possibly causes fast
(t,1.5 ms) electron transfer from heme d to heme b595 in a small fraction of the protein, not reported earlier. Then the
electron migrates to heme b558 (t,16 ms). It returns from the b-hemes to heme d with t,180 ms. Unlike cytochrome bd in
the R state, in MV enzyme the apparent contribution of absorbance changes associated with CO dissociation from heme d is
small, if any. Photodissociation of CO from heme d in MV enzyme is suggested to be accompanied by the binding of an
internal ligand (L) at the opposite side of the heme. CO recombines with heme d (t,16 ms) yielding a transient
hexacoordinate state (CO-Fe2+
-L). Then the ligand slowly (t,30 ms) dissociates from heme d. Recombination of CO with a
reduced heme b in a fraction of the MV sample may also contribute to the 30-ms phase. In R enzyme, CO recombines to
heme d (t,20 ms), some heme b558 (t,0.2–3 ms), and finally migrates from heme d to heme b595 (t,24 ms) in ,5% of the
enzyme population. Data are consistent with the recent nanosecond study of Rappaport et al. conducted on the
membranes at 640-nm excitation but limited to the Soret band. The additional phases were revealed due to differences in
excitation and other experimental conditions
ASFISSIA PERINATALE:VALUTAZIONE CLINICO-EPIDEMIOLOGICA IN UN CAMPIONE DI NEONATI DI ≥ 34 SEG
Asfissia, late preterm, a termin
Oxidative stress biomarkers and their relationship with cytokine concentrations in overweight/obese pregnant women and their neonates
Tratamento cirurgico do hidrocefalo em crianças: I - evolução clinica e mortalidade
Mechanisms involved in lung cancer development in COPD
Lung cancer and chronic obstructive pulmonary disease (COPD) are leading causes of morbidity and mortality worldwide. They share a common environmental risk factor in cigarette smoke exposure and a genetic predisposition represented by the incidence of these diseases in only a fraction of smokers. COPD is also a major independent risk factor for lung carcinoma, among long-term smokers. Smokers with COPD also have a higher risk of developing a specific histological subtype of non-small cell lung cancer termed squamous cell carcinoma. For these reasons the focus of this review is on the potential pathogenic molecular links between tobacco smoking-related COPD and squamous cell carcinoma. We believe that we need to promote more studies on the molecular and cellular pathobiology of smokers with premalignant bronchial lesions of the squamous cell lung carcinoma compared with a control group of smokers with and without COPD to unravel the complex molecular interactions between COPD and early squamous cell lung carcinoma. These studies should also look at younger healthy smokers in combination with risk models of lung cancer and COPD. Overall these studies may allow the discovery of new molecular targets of the early carcinogenesis process that in the foreseeable future may render the early diagnosis and treatment, and may be even the prevention, of invasive squamous cell lung carcinoma a reality
COPD pathology in the small airways
In the last quarter of century, the analysis of small airways specimens obtained from chronic obstructive pulmonary disease (COPD) patients compared with those from a control group of age-matched smokers with normal lung function has provided novel insights on the potential role of the different inflammatory and structural cells, pro/anti-inflammatory mediators and intracellular signalling pathways, contributing to a better knowledge of the pathogenesis of stable COPD. This also has provided a scientific rationale for new drugs discovery and targeting to the small airways. This review summarizes and discusses the pathology of small airways of stable COPD patients, of different severity, compared with control smokers with normal lung function
Phacoemulsification and intraocular lens in eyes with prymary angle-closure glaucoma:our experience.
Combined phacoemulsification and deep sclerectomy vs phacoemulsification and trabeculectomy.
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