Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: UMLS:C0032285 (pneumonia)
 54,520 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

1. In work along this line it is most important to have a simple method of determining the catalytic activity of tissues. The method must be such that several observations can be made during a single experiment, so that a better idea can be obtained of the velocity of the reaction at various intervals. 2. The catalytic activity of human tissues varies greatly in diseases. A. Nephritis.-The kidney always shows the most marked reduction although the other tissues examined, blood, lung, liver, spleen, likewise show decrease in their power of decomposing hydrogen peroxide. This reduction varies directly with the severity of the pathological lesion in the kidney and the clinical symptoms. The urine also in cases of nephritis shows a much greater inhibiting power than normal urine. This may be accounted for by the reaction of the urine, and subsequent work must prove whether or not the kidney takes any more active part in nephritis and secretes into the blood and urine a substance which manifests itself by a reduction in the catalytic activity. B. The catalytic activity of the blood in the two cases of eclampsia which we have studied was not reduced. This is the most important fact we have so far obtained, if it can be substantiated, since it can furnish us with a ready ante-mortem means of differentiating eclampsia and nephritis. C.Pneumonia.-The lung in the stage of red hepatization has an increased catalytic activity. This increase varies directly with the number of intact red blood cells in the exudate, and in the engorged capillaries. Strength is given to this conclusion by the fact, that on the one hand, there is no increased activity in gray hepatization, while on the other hand, there is an enormously increased activity in the fresh hemorrhagic infarct. D. Tuberculosis.-The decreased activity of the lung in tuberculosis is probably due, for the most part, to the lack of blood in the diseased area, while the lowered activity which is present in the other organs is to be explained by the anaemia and emaciation which accompanies the process. Whether there is a specific catalytic inhibiting substance generated by the process, has not been determined. E. There was no reduction of the catalytic activity in the cases of diabetes mellitus and jaundice studied. F. In the one case of asphyxiation by illuminating gas, there was decided decrease in the catalytic activity of the blood. G. The tissues in the one case of congenital syphilis showed a marked lowering of the catalytic activity. 3. There is a slight decrease in the catalytic activity of the tissues due to post-mortem change, but this is so slight that it is hardly to be taken into consideration in the interpretation of the results obtained. 4. There is no marked change in the catalytic activity due to age. In concluding, we wish to thank Dr. A. S. Loevenhart, at whose suggestion this enzyme was studied, for the unfailing interest with which he has followed the progress of this work, and for the many valuable suggestions he has given us.
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PMID:ON THE OCCURRENCE OF CATALASE IN HUMAN TISSUES AND ITS VARIATIONS IN DISEASES. 1986 62

Evidence is given of the presence in the cellular material obtained from the pneumonic lung of a proteolytic enzyme digesting coagulated blood serum at hydrogen ion concentrations of 7.3 to 6.7 and inactive at higher; i.e., more acid concentrations. In addition, evidence is brought forward of the presence in the cellular material from the pneumonic lung of a proteolytic enzyme splitting peptone to amino-acid nitrogen. This enzyme is operative at hydrogen ion concentrations from 8.0 to 4.8, but most active at 6.3 or 5.2. These findings may be regarded as having a bearing on resolution in pneumonia. During the course of the disease a gradual increase in the hydrogen ion concentration of the exudate probably takes place. With the breaking down of cellular material an enzyme digesting protein (fibrin) in weakly alkaline and weakly acid media may be liberated. With a gradual increase in the hydrogen ion concentration of the pneumonic lung the action of this enzyme probably ceases. An enzyme capable of splitting peptone to amino-acid nitrogen is probably active during the proteolysis of the fibrin and further activated when the hydrogen ion concentration of the pneumonic lung is increased to within its range of optimum activity at a pH of 6.3 and 5.2. By this means it may be conceived that the exudate is dissolved and resolution takes place.
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PMID:THE RELATION OF PROTEOLYTIC ENZYMES IN THE PNEUMONIC LUNG TO HYDROGEN ION CONCENTRATION. AN EXPLANATION OF RESOLUTION. 1986 65

It has been possible to study the cultural characters and certain of the immunological relationships of sixteen strains of Bacillus bovisepticus. The organisms have fallen into three distinct cultural groups. The largest group comprises eight strains, four of them obtained in pure cultures from cases of pneumonia in cows, two others were pure infections in calves, the others were associated with other organisms. This group may be characterized as short, non-motile, Gram-negative, encapsulated rods which fail to produce indole but produce clear zones about the deep colonies in horse blood agar plate cultures. Members of this group produce acid in media containing dextrose, lactose, saccharose, maltose, and mannitol. The final hydrogen ion concentration in dextrose broth lies between pH 6.3 and 6.1. The next largest aggregation comprises six strains. These organisms ferment dextrose and saccharose, but do not attack lactose, maltose, or mannitol. All produce indole. All are soluble in ox and guinea pig bile but none are hemolytic. The other two strains resemble the preceding but attack mannitol in addition to dextrose and saccharose. They produce indole but are not bile-soluble. In the main the immunological relationship has been found to follow cultural grouping. All of Group I are agglutinated by a serum prepared by immunizing a rabbit with a single Group I strain. This serum fails to agglutinate members of other groups. The same holds true with Group II and III sera. In no instance has cross-agglutination between groups taken place.
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PMID:A STUDY OF BACILLUS BOVISEPTICUS. 1986 78

The hydrogen ion concentration in the lesions of experimental pneumococcus infection has been estimated directly by pH determinations on exudates from living animals. For indirect evidence of an increase in hydrogen ion concentration within the lesions, the difference in sugar content between exudate and blood from animals with pneumococcus infection has been measured. With sanguinous exudate from the consolidated lungs of dogs with experimental pneumococcus pneumonia, the findings were not always consistent, but usually there was either direct or indirect evidence of increased hydrogen ion concentration. The physicochemical changes in exudate from animals treated with artificial pneumothorax showed no important differences from those in other specimens. In concurrence with Lord's (1, 2) observation of increased acidity in pneumonia exudate obtained at autopsy, sugar concentrations, which are low in the blood, were markedly reduced in exudates from animals which had died of the infection. Serous exudates from dermal pneumococcus infection in rabbits uniformly showed definite acidity by both direct and indirect methods of estimation. The hydrogen ion concentrations in exudate from dermal pneumococcus infection in rabbits varied between pH 6.87 and 6.66 but were not always proportional to the difference in sugar concentrations between the exudate and blood. While these hydrogen ion concentrations are similar to those attained in the pneumonic exudate from dogs, they are of lesser magnitude than those which Takahashi (3) has described in the pus of secondary empyema due to the pneumococcus.
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PMID:HYDROGEN ION CONCENTRATION IN EXUDATES OF PNEUMOCOCCUS INFECTION. 1987 Jul 46

Biofilm formation has been suggested to play an important role during Streptococcus pneumoniae nasopharyngeal colonization and may facilitate progression to pneumonia. To test whether the ability of S. pneumoniae to form biofilms was important for virulence we screened the ability of 30 invasive and 22 non-invasive clinical isolates of serotype 6A and 6B to form early biofilms on polystyrene microtiter plates and infect mice following intranasal and intratracheal challenge. We first determined that no correlation existed between the ability to form early biofilms and whether isolates were collected from healthy carriers or individuals with invasive disease. A disconnect between biofilm forming ability and the capacity to colonize the nasopharynx, cause pneumonia, and enter the bloodstream was also observed in mice. Importantly, S. pneumoniae mutants deficient in the established virulence determinants pneumolysin, CbpA, and hydrogen peroxide formed biofilms normally. Incidentally, we determined that robust biofilm production was dependent on the formation and coalescing of bacterial aggregates on a thin layer of bacteria attached to the plate surface. In summary, these studies suggest that the ability to form early biofilms in vitro does not reflect virulence potential. More complex studies are required to determine if biofilm formation is important for virulence.
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PMID:Early biofilm formation on microtiter plates is not correlated with the invasive disease potential of Streptococcus pneumoniae. 2009 71

A study of 10 infants in severe metabolic acidemia (pH below 7) led to the conclusion that the clinical signs-hyperventilation, coma or lethargy, peripheral vascular collapse, a significantly palpable liver, and abdominal distension-may all be directly related to the metabolic acidemia. In five of 10 infants, an initial erroneous diagnosis of congestive heart failure or pneumonia was made. Dramatic clinical improvement followed correction of the acidemia with rapid intravenous administration of sodium bicarbonate. This rapid administration of sodium bicarbonate was safe, provided hypocalcemia was recognized and treated in its early stages. In severe metabolic acidemia the measurement of blood bicarbonate alone does not reflect adequately the magnitude of the acid-base derangement and repeated measurements of hydrogen ion concentration, Pco(2) and bicarbonates are needed to evaluate and treat such infants correctly.
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PMID:Severe metabolic acidemia in infants: clinical and therapeutic aspects. 2032 90

Lung innate immune response plays an important role in the clearance of pathogens from lungs, however, profound activation of innate immune cells (alveolar macrophages or neutrophils) can lead to development of acute lung inflammation or injury by producing various pro-inflammatory molecules (IL-1, TNF-alpha and H2O2 etc.). Present study is designed to investigate the immunomodulatory action of thalidomide in Klebsiella pneumoniae B5055 induced acute lung infection in BALB/c mice. Acute lung inflammation was induced by intranasal instillation of K. pneumoniae B5055 into mice without any anaesthesia and treated with thalidomide (30 mg/kg/day/po) or normal saline orally using a treatment schedule shown to modulate pro-inflammatory innate immune response. Thalidomide treatment modulated pro-inflammatory function of alveolar macrophages by significantly (p<0.05) decreasing their phagocytic potential in terms of phagocytic uptake and intracellular killing, spreading and hydrogen peroxide (H2O2) release. Besides that thalidomide treatment also significantly (p<0.05) decreased neutrophil infiltration into the lung alveoli. Remarkably, the levels of pro-inflammatory cytokines (IL-1alpha and TNF-alpha) were found to be decreased significantly (p<0.05) in thalidomide treated group but the levels of IL-10 were found to be significantly (p<0.05) elevated. Thus thalidomide proved a promising immunomodulatory agent in acute lung inflammation associated with pneumonia caused by gram negative bacterial infection.
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PMID:Thalidomide treatment modulates macrophage pro-inflammatory function and cytokine levels in Klebsiella pneumoniae B5055 induced pneumonia in BALB/c mice. 2039 10

The functional sites were predicted for Nudix enzymes from pathogenic microorganisms such as Streprococcus pneumonia (2B06) and Enterococcus faecalis (2AZW). Their structures are already determined, however, no data is reported about their functional sites, substrates and inhibitors. Therefore, we report prediction of functional sites in these Nudix enzymes via Geometric Invariant (GI) technique (Construct different geometries of peptides which remain unchanged). The GI method enumerated 2B06: RA57, EA58, EA61, EA62 and 2AZW: RA62, EA63, EA66, EA67 as putative functional sites in these Nudix enzymes. In addition, the substrate was predicted via Molecular docking (Docking of substrates against whole structure of Nudix enzymes). The substrate ADP-Ribose was docked with the Nudix enzymes, 2B06 (Docking energy -15.68 Kcal/mol) and 2AZW (Docking energy -10.86 Kcal/mol) with the higher affinity and the lower docking energy as compared to other substrates. The residues EA62 in 2B06 and RA62 in 2AZW make hydrogen bonds with the ADP-ribose. Furthermore, we screened 51 inhibitor compounds against structures of 2B06 and 2AZW. The inhibitor compounds AMPCPR and CID14258187 were docked well as compared to other compounds. The compound CID14258187 was also in agreement with Lipinski rule of 5 for drug likeness properties. Therefore, our findings of functional sites, substrates and inhibitors for these Nudix enzymes may help in structure based drug designing against Streprococcus pneumonia and Enterococcus faecalis.
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PMID:Structure based prediction of functional sites with potential inhibitors to Nudix enzymes from disease causing microbes. 2138 22

This study examined the relationship between volatile sulfur compounds (VSCs), including hydrogen sulphide (H(2)S), methyl mercaptan (CH(3)SH) and dimethyl sulphide [(CH(3))(2)S], in mouth air of patients and a history of systemic disease. The subjects were 387 residents (174 males and 213 females) of Fukuoka Prefecture, Japan, who participated in an oral and systemic health survey for elderly persons (mean age: 61.8, s.d. 2.8 years). The VSCs were measured using a portable gas chromatograph (OralChroma). The H(2)S concentrations were significantly greater in the 132 subjects with a history of hypertension and the 41 subjects with a history of respiratory disease, including pneumonia, pulmonary emphysema and bronchitis, than in those without such a history. The CH(3)SH concentrations were significantly greater in those with a history of hypertension. The 16 subjects with a history of cerebrovascular disease, including intracerebral haemorrhage, cerebral infarction, and subarachnoid haemorrhage, and the 58 subjects with a history of liver disease, including hepatitis, alcoholic liver disease, drug-induced liver injury, fatty liver and liver cirrhosis, showed significantly greater (CH(3))(2)S concentrations (p < 0.05). These results suggest an association between the production of VSCs in mouth air and systemic diseases such as hypertension as well as respiratory, cerebrovascular and liver diseases.
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PMID:Relationship between volatile sulfur compounds in mouth air and systemic disease. 2138 56

Radiotherapy is an important modality of cancer treatment. Radiation pneumonitis is a major obstacle to increasing the radiation dose in radiotherapy, and it is important to prevent this radiation-induced complication. Recent studies show that hydrogen has a potential as an effective and safe radioprotective agent by selectively reducing hydroxyl and peroxynitrite radicals. Since most of the ionizing radiation-induced cellular damage is caused by hydroxyl radicals, we hypothesize that a treatment combining radiotherapy with aerosol inhalation of a hydrogen-rich solution may be an effective and novel prevention strategy for radiation pneumonitis (hydrogen is explosive, while a hydrogen-rich solution such as physiological saline saturated with molecular hydrogen is safer).<br />
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PMID:A possible prevention strategy of radiation pneumonitis: combine radiotherapy with aerosol inhalation of hydrogen-rich solution. 2145 14


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