scholarly journals On the Digestive Action of Leucocytes, Pus and Body Exudates

1934 ◽  
Vol 34 (1) ◽  
pp. 99-117 ◽  
Author(s):  
Leonard S. Dudgeon ◽  
L. T. Bond

1. Eighty-seven specimens of septic pus obtained from patients suffering from recent and old infections were examined fully bacteriologically and cytologically and were sterilised at 60° C. for 2 or 4 hours. The heated samples of pus were used for our experiments.2. Glycerine extracts were prepared of the pus by two methods referred to in detail in the text.3. The digestive action of the samples of sterile pus and of their glycerine extracts were tested on inspissated blood serum, gelatin, milk, egg and hydrocele saline. Digestion occurred on all these media in varying degrees with the specimens of pus, but glycerine extracts were more active.4. It was found that the addition of pus or glycerine extracts of pus with various strains of Bacillus typhosus, B. paratyphosus A, B and C, B. gaertner and B. shiga to milk, produced clotting of the medium at 37° C. in the majority of our experiments.5. If pus was heated at 60° C. for as long as 6 hours its digestive manifestations were not affected, but 80° C. for 20 min. or 100° C. for 10 min. completely destroyed the digestive activity.6. At 22° C. the digestive action of pus was weakly manifested, while in the ice chest no reaction whatever took place.7. Clotting of the medium occurred when pus was added to killed growths of B. typhosus and B. paratyphosus A in milk, but not with B. paratyphosus B or B. gaertner.8. Human milk did not clot with pus and these organisms.9. A large number of observations were made with serum exudates from pus, either after filtering through a Seitz E.K. filter or after heating at 60° C. It was found that the filtered or heated fluids might have a similar or a weaker action as compared with pus, or they might be inhibitory.10. The white cells from several cases of chronic myeloid leukaemia, chronic lymphatic, the myeloblastic termination of chronic myeloid and acute leukaemia, were examined in the same manner as pus. The cells of chronic myeloid leukaemia acted in every way like pus, those of chronic lymphatic and their glycerine extracts were quite inactive; those of acute leukaemia corresponded to chronic lymphatic, while those of a myeloblastic termination gave a weak digestive reaction.11. Specimens of blood serum from normal human beings and from patients with acute infections, and some specimens of body fluids before and after filtering, were found to inhibit the clotting of milk inoculated with pus and the microbes.12. Twenty-two specimens of tuberculous pus obtained from abscesses and from pyo-pneumothorax, and seven samples of tuberculous sputum, were examined fully, but with special reference to their cytology.In eight cases the pus showed no digestive action and no clotting of milk with the microbes, in nine cases a feeble reaction occurred, and in five cases the reactions were like those of pyogenic pus. Thus seventeen of the specimens could bedistinguished readily from pyogenic pus; in the five positive specimens polymorphs were numerous, but one of these cases was complicated by a secondary infection. In every sample of tuberculous sputum polymorphs and tubercle bacilli were numerous and the reactions corresponded to those of pyogenic pus.

Author(s):  
Lisa Repsold ◽  
Roger Pool ◽  
Mohammed Karodia ◽  
Gregory Tintinger ◽  
Piet Becker ◽  
...  

1989 ◽  
Vol 82 (4) ◽  
pp. 205-209 ◽  
Author(s):  
L.M. Secker-Walker ◽  
H.M. Cooke ◽  
P.J. Browett ◽  
J.D. Norton ◽  
C. Kitchen ◽  
...  

2000 ◽  
Vol 111 (1) ◽  
pp. 292-302 ◽  
Author(s):  
Philippe Guardiola ◽  
Mathieu Kuentz ◽  
Frederic Garban ◽  
Didier Blaise ◽  
Josy Reiffers ◽  
...  

2000 ◽  
Vol 111 (1) ◽  
pp. 292-302 ◽  
Author(s):  
Philippe Guardiola ◽  
Mathieu Kuentz ◽  
Frédéric Garban ◽  
Didier Blaise ◽  
Josy Reiffers ◽  
...  

1994 ◽  
Vol 71 (01) ◽  
pp. 091-094 ◽  
Author(s):  
M Cattaneo ◽  
B Akkawat ◽  
R L Kinlough-Rathbone ◽  
M A Packham ◽  
C Cimminiello ◽  
...  

SummaryNormal human platelets aggregated by thrombin undergo the release reaction and are not readily deaggregated by the combination of inhibitors hirudin, prostaglandin E1 (PGE1) and chymotrypsin. Released adenosine diphosphate (ADP) plays an important role in the stabilization of thrombin-induced human platelet aggregates. Since ticlopidine inhibits the platelet responses to ADP, we studied thrombin-induced aggregation and deaggregation of 14C-serotonin-labeled platelets from 12 patients with cardiovascular disease before and 7 days after the oral administration of ticlopidine, 250 mg b.i.d. Before and after ticlopidine, platelets stimulated with 1 U/ml thrombin aggregated, released about 80–90% 14C-serotinin and did not deaggregate spontaneously within 5 min from stimulation. Before ticlopidine, hirudin (5× the activity of thrombin) and PGE1 (10 μmol/1) plus chymotrypsin (10 U/ml) or plasmin (0.06 U/ml), added at the peak of platelet aggregation, caused slight or no platelet deaggregation. After ticlopidine, the extent of platelet deaggregation caused by the same inhibitors was significantly greater than before ticlopidine. The addition of ADP (10 μmol/1) to platelet suspensions 5 s after thrombin did not prevent the deaggregation of ticlopidine-treated platelets. Thus, ticlopidine facilitates the deaggregation of thrombin-induced human platelet aggregates, most probably because it inhibits the effects of ADP on platelets.


2018 ◽  
Vol 2 (02) ◽  
pp. 39-41
Author(s):  
Md. Rafiquzzaman Khan ◽  
Arifur Rahman ◽  
Khaza Amirul Islam ◽  
AQM Ashraful Haque ◽  
Masuda Begum

The aim of this retrospective observational study was to observe the pattern and frequency of haematological disorders among the patients attending in the specialized Haematology outpatient Department (HOPD) in Bangabandhu Sheikh Mujib Medical University. Consecutive 201 patients over the period of one year were enrolled. Their age ranged from 01 to 72 years with a mean age of 36.76 years. Most of the patients (34.3%) were in between the ages of 31 to 45 years followed by 16 to 30 years (27.9%). Male to female ratio was 0.65. Iron deficiency anaemia is the most common (24.9%) followed by chronic myeloid leukaemia (11.9%), Hb E beta thalassaemia (9.5%), idiopathic thrombocytopenic purpura (9.5%), beta thalassaemia trait (7.0%), Hb E trait (5.5 %), aplastic anaemia (5.0%), multiple myeloma (3.5%), acute lymphoblastic leukaemia (3.0%). Acute myeloid leukaemia, autoimmune haemolytic anaemia, chronic lymphocytic leukaemia, anaemia of chronic disease, non-Hodgkin lymphoma, polycythaemia, beta thalassemia major and alpha thalassemia was 2.5%, 2.5%, 2.0%, 1.5%, 1.5%, 1.5%, 1.0% and 1.0%, respectively. In the present study, we observed that iron deficiency anaemia the most common non-malignant disease and chronic myeloid leukaemia is the common haematological malignancy.


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