scholarly journals TOXIN AND ANTITOXIN OF AND PROTECTIVE INOCULATION AGAINST BACILLUS WELCHII

1917 ◽  
Vol 26 (1) ◽  
pp. 119-138 ◽  
Author(s):  
Carroll G. Bull ◽  
Ida W. Pritchett
Keyword(s):  
Sodium Hydroxide ◽  
Blood Stream ◽  
Immune Serum ◽  
Rabbit Muscle ◽  
Active Immunity ◽  
Curative Action ◽  
Toxic Constituent ◽  
Bacterial Emboli

Five cultures of Bacillus welchii have been studied and compared Four came from infected wounds in the western theatre of war, and one was obtained from a personal article of clothing. Each culture possesses the essential characteristics ascribed to that group of bacteria. The infectious processes caused by the five cultures in rabbits, guinea pigs, and pigeons, are local in character; and very few or no bacilli enter or are found in the general blood stream during life or immediately after death. Glucose broth cultures, injected intravenously, are fatal to rabbits. Death occurs, almost immediately or after a few hours. Agglutinative bacterial emboli have been ruled out as the cause of death, as has been an acid intoxication. The fluid part of the culture acts in the same manner as the full culture and irrespective of neutralization with sodium hydroxide. The full cultures and supernatant fluid are hemolytic when injected directly into the circulation of rabbits and pigeons, and the acute death produced may be ascribed to a massive destruction of red corpuscles. The passage of the fluid portion of glucose broth cultures through Berkefeld filters reduces materially the hemolytic and poisonous effects. Cultures of the Welch bacilli in plain broth to which sterile pigeon or rabbit muscle is added are highly toxic, and the toxicity is not noticeably diminished by Berkefeld filtration. The filtrates are hemolytic when injected intravenously and inflaming and necrotizing when injected subcutaneously and intramuscularly. The local lesions produced in the breast muscles of the pigeon closely resemble those caused by infection with the bacilli. The toxicity of these filtrates is not affected by neutralization with sodium hydroxide, but is materially reduced by heating to 62°C. and entirely removed by heating to 70°C. for 30 minutes. Successive injections of carefully graded doses of this toxic filtrate in pigeons and rabbits give rise to active immunity. The blood taken from the immunized rabbits is capable of neutralizing the toxic filtrate in vivo and in vitro. The filtrate has therefore been designated as toxin and the immune serum as antitoxin. The antitoxin neutralizes the toxin in multiple proportions. Hence the latter would seem to possess the properties of an exotoxin. Moreover, it neutralizes the hemolytic as well as the locally .injurious toxic constituent. Antitoxic serum prepared from a given culture of Bacillus welchii is neutralizing for the toxins yielded by the other four cultures of that microorganism. The antitoxin is protective and curative against infection with the spore and the vegetative stages of Bacillus welchii in pigeons. The limits of the protective and curative action are now under investigation.

scholarly journals Effect of cannulation site on emboli travel during cardiac surgery

2021 ◽  
Vol 16 (1) ◽  
Author(s):  
Mira Puthettu ◽  
Stijn Vandenberghe ◽  
Stefanos Demertzis
Keyword(s):  
Cardiac Surgery ◽  
In Vitro Study ◽  
Blood Stream ◽  
Air Bubbles ◽  
Arterial Tree ◽  
Air Bubble ◽  
Cannulation Site ◽  
The Brain

Abstract Background During cardiac surgery, micro-air emboli regularly enter the blood stream and can cause cognitive impairment or stroke. It is not clearly understood whether the most threatening air emboli are generated by the heart-lung machine (HLM) or by the blood-air contact when opening the heart. We performed an in vitro study to assess, for the two sources, air emboli distribution in the arterial tree, especially in the brain region, during cardiac surgery with different cannulation sites. Methods A model of the arterial tree was 3D printed and included in a hydraulic circuit, divided such that flow going to the brain was separated from the rest of the circuit. Air micro-emboli were injected either in the HLM (“ECC Bubbles”) or in the mock left ventricle (“Heart Bubbles”) to simulate the two sources. Emboli distribution was measured with an ultrasonic bubble counter. Five repetitions were performed for each combination of injection site and cannulation site, where air bubble counts and volumes were recorded. Air bubbles were separated in three categories based on size. Results For both injection sites, it was possible to identify statistically significant differences between cannulation sites. For ECC Bubbles, axillary cannulation led to a higher amount of air bubbles in the brain with medium-sized bubbles. For Heart Bubbles, aortic cannulation showed a significantly bigger embolic load in the brain with large bubbles. Conclusions These preliminary in vitro findings showed that air embolic load in the brain may be dependent on the cannulation site, which deserves further in vivo exploration.

scholarly journals A SPECIFIC POISON IN THE LIVER EXTRACTS OF RABBITS INOCULATED WITH TYPHOID AND PRODIGIOSUS BACILLI INTRAVENOUSLY

1918 ◽  
Vol 28 (5) ◽  
pp. 571-583
Author(s):  
Julia T. Parker
Keyword(s):  
Anaphylactic Shock ◽  
Liver Extract ◽  
Lethal Dose ◽  
Toxic Substance ◽  
Normal Liver ◽  
Immune Serum ◽  
Minimum Lethal Dose ◽  
Lethal Doses

1. The livers of rabbits inoculated with cultures of Bacillus typhosus or Bacillus prodigiosus under certain conditions contain a toxic substance extractable with salt solution. When the toxic extracts are injected intravenously into normal rabbits the latter animals develop symptoms resembling those of anaphylactic shock and succumb. The lethal doses of the toxic extracts are far smaller than those of normal liver extract. 2. The livers of rabbits injected with typhoid antigen also yield a toxic extract. 3. Boiling as well as filtration through a Berkefeld filter only partially detoxicates the extract. 4. Tolerance to one to two lethal doses of the poisonous extracts can be induced by cautious immunization. 5. Rabbits actively immunized to Bacillus typhosus or Bacillus prodigiosus usually resist one lethal dose of the homologous liver poison; and animals tolerant to the typhoid liver poison resist one minimum lethal dose at least of Bacillus typhosus. 6. Typhoid immune serum is not detoxicating either in vivo or in vitro for the typhoid liver poison. 7. The liver poisons are specific, since rabbits actively immunized to either Bacillus typhosus or Bacillus prodigiosus withstand at least one minimum lethal dose of the homologous but not of the heterologous-liver poisons.

scholarly journals THE EFFECT OF RHEUMATOID FACTORS AND OF ANTIGLOBULINS ON IMMUNE HEMOLYSIS IN VIVO

1963 ◽  
Vol 117 (1) ◽  
pp. 105-125 ◽  
Author(s):  
Manuel E. Kaplan ◽  
James H. Jandl
Keyword(s):  
Protein Content ◽  
Blood Stream ◽  
Body Fluids ◽  
Red Cells ◽  
Rheumatoid Factors ◽  
Low Protein ◽  
Immune Hemolysis

Studies were undertaken in man and in the rat comparing the effects of rheumatoid factors and immune antiglobulins on red cells sensitized with incomplete antibodies. The interaction of immune antiglobulins with sensitized red cells produced (a) agglutination in vitro and (b) an accelerated sequestration of the sensitized cells in vivo. In contrast, rheumatoid macroglobulins, although capable of agglutinating Rh-sensitized red cells in vitro, did not modify their destruction in vivo. The failure of rheumatoid factors to function as antiglobulins in vivo appears to reflect their non-reactivity with sensitized cells in whole serum. It is suggested: (a) that the native (7S) gamma globulins of plasma competitively inhibit rheumatoid factors from reacting with fixed antibody in the blood stream; (b) that if these macroglobulins do indeed have pathogenetic activity, this may be limited to body fluids of low protein content.

scholarly journals The MEMIC: An ex vivo system to model the complexity of the tumor microenvironment

2021 ◽  
Author(s):  
Libuše Janská ◽  
Libi Anandi ◽  
Nell C. Kirchberger ◽  
Zoran S. Marinkovic ◽  
Logan T. Schachtner ◽  
...  
Keyword(s):  
Tumor Microenvironment ◽  
Tumor Cells ◽  
Ex Vivo ◽  
Tumor Stroma ◽  
Stem Cell Differentiation ◽  
Blood Stream ◽  
Direct Access ◽  
Ex Vivo Model

There is an urgent need for accurate, scalable, and cost-efficient experimental systems to model the complexity of the tumor microenvironment. Here, we detail how to fabricate and use the Metabolic Microenvironment Chamber (MEMIC) – a 3D-printed ex vivo model of intratumoral heterogeneity. A major driver of the cellular and molecular diversity in tumors is the accessibility to the blood stream that provides key resources such as oxygen and nutrients. While some tumor cells have direct access to these resources, many others must survive under progressively more ischemic environments as they reside further from the vasculature. The MEMIC is designed to simulate the differential access to nutrients and allows co-culturing different cell types, such as tumor and immune cells. This system is optimized for live imaging and other microscopy-based approaches, and it is a powerful tool to study tumor features such as the effect of nutrient scarcity on tumor-stroma interactions. Due to its adaptable design and full experimental control, the MEMIC provide insights into the tumor microenvironment that would be difficult to obtain via other methods. As a proof of principle, we show that cells sense gradual changes in metabolite concentration resulting in multicellular spatial patterns of signal activation and cell proliferation. To illustrate the ease of studying cell-cell interactions in the MEMIC, we show that ischemic macrophages reduce epithelial features in neighboring tumor cells. We propose the MEMIC as a complement to standard in vitro and in vivo experiments, diversifying the tools available to accurately model, perturb, and monitor the tumor microenvironment, as well as to understand how extracellular metabolites affect other processes such as wound healing and stem cell differentiation.

A Comparative Study of Bioceramics In Vitro and In Vivo

2005 ◽  
Vol 284-286 ◽  
pp. 11-14 ◽  
Author(s):  
Yang Leng ◽  
Ren Long Xin ◽  
Ji Yong Chen
Keyword(s):  
Calcium Phosphates ◽  
Glass Ceramics ◽  
Octacalcium Phosphate ◽  
Rabbit Muscle ◽  
In Vivo Experiments ◽  
Transmission Electron ◽  
Diffraction Patterns ◽  
Dental Applications

Bioactive calcium phosphate (Ca-P) formation in bioceramics surfaces in simulated body fluid (SBF) and in rabbit muscle sites was investigated. The examined bioceamics included most commonly used bioglass®, A-W glass-ceramics and calcium phosphates in orthopedic and dental applications. The Ca-P cyrstal structures were examined with single crystal diffraction patterns in transmission electron microscopy, which reduced possibility of misidentifying Ca-P phases. The experimental results show that capability of Ca-P formation considerably varied among bioceramics, particularly in vivo. Octacalcium phosphate (OCP) was revealed on the all types of bioceramics in vitro and in vivo experiments. This work leads us to rethink how to evaluate bioactivity of bioceramics and other orthopedic materials which exhibit capability of osteoconduction by forming direct bonding with bone.

scholarly journals A novel in vitro model of metastasis supporting passive shedding hypothesis from murine pancreatic cancer Panc-02

2019 ◽  
Vol 71 (5) ◽  
pp. 989-1002
Author(s):  
M. P. Krzykawski ◽  
R. Krzykawska ◽  
M. Paw ◽  
J. Czyz ◽  
J. Marcinkiewicz
Keyword(s):  
Pancreatic Cancer ◽  
Cell Line ◽  
Cancer Metastasis ◽  
Metastatic Potential ◽  
Blood Stream ◽  
Culture Surface ◽  
Vitro Model ◽  
In Vitro Cell Cultures

Abstract Cancer metastasis is believed to happen through active intravasation but there might be also another way to metastasize. According to passive shedding hypothesis, proposed by Munn et al., tumor cells detach from the tumor mass and passively shed to blood stream through leaky blood vessels. We propose a novel In Vitro Migrational Selection (IVMS) assay that enables the pre-selection of invasive pancreatic cancer Panc-02 cells and create a model of passive shedding. We established invasive sub-cell line of murine pancreatic cancer Panc-02 cells (refered to as Panc02-RS), which exhibited higher metastatic potential in vivo and at the same time decrease in vitro migratory skills, comparing to the initial Panc-02 cell line. In in vitro cell cultures Panc-02 spontaneously detached from the cell culture surface and later reattached and colonized new areas. We believe it can mimic the new way of metastasis, namely passive shedding. We concentrated on Panc-02 model but believe that IVMS might be used to create sub cell lines of many solid tumors to model passive shedding. Our results support the passive shedding hypothesis.

scholarly journals Anoikis Resistance as a Further Trait of Acidic-Adapted Melanoma Cells

2019 ◽  
Vol 2019 ◽  
pp. 1-13 ◽  
Author(s):  
Silvia Peppicelli ◽  
Jessica Ruzzolini ◽  
Francesca Bianchini ◽  
Elena Andreucci ◽  
Chiara Nediani ◽  
...  
Keyword(s):  
Blood Stream ◽  
Melanoma Cells ◽  
Extracellular Ph ◽  
Cloning Efficiency ◽  
Anoikis Resistance ◽  
Additional Mechanism ◽  
Medium Ph ◽  
Aggressive Cancer

Melanoma is characterized by a low extracellular pH, which contributes to the development of an aggressive phenotype characterized by several properties as the switch to an epithelial-to-mesenchymal program, the increase of apoptotic resistance, and the migratory ability together with the development of drug resistance. Here, we demonstrate that melanoma cells grown in low pH medium (pH 6.7) for a short (24 hours) or long (at least 3 months) period equally express an anoikis resistance profile. Anoikis is a form of apoptosis prompted by loss of adhesion, particularly requested by aggressive cancer cells to metastasize. Anoikis resistance was ascertained in acidic melanoma cells either grown in agarose-coated plates or incubated in rocking conditions. Both analyses indicate that acidic cells were more able to survive in a nonadherent condition than cells grown in standard pH, an effect resulting in a more cloning efficiency and migratory ability. Ability to survive during rocking was inhibited using mTOR/NF-kB inhibitors. Finally, we checked whether characteristics related to thein vitroanoikis resistance acquired by acidic melanoma cells might be also suitable forin vivochallenge. We injected acidic melanoma cells into blood stream, and then we verify how many cells survived in blood after 15 min from the injection. Only acidic cells, transient and chronic, survived, whereas melanoma cells grown in standard pH medium did not. Overall, we have had the opportunity to demonstrate that low extracellular pH represents an additional mechanism able to promote an anoikis resistance in solid tumors.

scholarly journals Immunologic Aspects of the Biogenesis of Erythropoietin

Blood ◽  
1970 ◽  
Vol 35 (3) ◽  
pp. 276-281 ◽  
Author(s):  
JOHN C. SCHOOLEY ◽  
ESMAIL D. ZANJANI ◽  
ALBERT S. GORDON
Keyword(s):  
Immune Serum ◽  
Serum Substrate

Abstract Immunologic evidence is presented that the interaction of Renal Erythropoietic Factor (REF) and a serum substrate results in the production in vitro of erythropoietin. Antibody capable of neutralizing erythropoietin (ESF) does not combine with either the REF or the serum substrate. Immune serum against the crude REF extract has been produced. This immune serum does not prevent the in vitro action or in vivo production of REF. This failure, however, may result from the diversity of antibodies produced.

scholarly journals The fate of a designed protein corona on nanoparticles in vitro and in vivo

2015 ◽  
Vol 6 ◽  
pp. 36-46 ◽  
Author(s):  
Denise Bargheer ◽  
Julius Nielsen ◽  
Gabriella Gébel ◽  
Markus Heine ◽  
Sunhild C Salmen ◽  
...  
Keyword(s):  
Superparamagnetic Iron Oxide ◽  
Protein Corona ◽  
Blood Stream ◽  
Minor Importance ◽  
Iron Oxide Particles ◽  
Corona Formation ◽  
The Stability ◽  
Covalently Bound

A variety of monodisperse superparamagnetic iron oxide particles (SPIOs) was designed in which the surface was modified by PEGylation with mono- or bifunctional poly(ethylene oxide)amines (PEG). Using 125I-labeled test proteins (transferrin, albumin), the binding and exchange of corona proteins was studied first in vitro. Incubation with 125I-transferrin showed that with increasing grade of PEGylation the binding was substantially diminished without a difference between simply adsorbed and covalently bound protein. However, after incubation with excess albumin and subsequently whole plasma, transferrin from the preformed transferrin corona was more and more lost from SPIOs in the case of adsorbed proteins. If non-labeled transferrin was used as preformed corona and excess 125I-labeled albumin was added to the reaction mixtures with different SPIOs, a substantial amount of label was bound to the particles with initially adsorbed transferrin but little or even zero with covalently bound transferrin. These in vitro experiments show a clear difference in the stability of a preformed hard corona with adsorbed or covalently bound protein. This difference seems, however, to be of minor importance in vivo when polymer-coated 59Fe-SPIOs with adsorbed or covalently bound 125I-labeled mouse transferrin were injected intravenously in mice. With both protein coronae the 59Fe/125I-labelled particles were cleared from the blood stream within 30 min and appeared in the liver and spleen to a large extent (>90%). In addition, after 2 h already half of the 125I-labeled transferrin from both nanodevices was recycled back into the plasma and into tissue. This study confirms that adsorbed transferrin from a preformed protein corona is efficiently taken up by cells. It is also highlighted that a radiolabelling technique described in this study may be of value to investigate the role of protein corona formation in vivo for the respective nanoparticle uptake.

Sodium hydroxide treatment of barley straw; effect of volume and concentration of solution on digestibility and intake by sheep

1975 ◽  
Vol 21 (3) ◽  
pp. 313-322 ◽  
Author(s):  
M. C. N. Jayasuriya ◽  
Emyr Owen
Keyword(s):  
Sodium Hydroxide ◽  
Barley Straw ◽  
Naoh Solution ◽  
Effect Of Treatment ◽  
Ad Libitum ◽  
Subsequent Neutralization ◽  
Male Sheep ◽  
Sodium Hydroxide Treatment

SUMMARY1. Four experiments have been carried out to determine the effect of treatment of spring-sown barley straw (var. Deba Abed) with sodium hydroxide (NaOH) solution and subsequent neutralization with hydrochloric acid (HCl) on its digestibility and intake by sheep.2. In Experiment 1, chopped straw was mixed with 4·5 or 9·0 g NaOH in 200 or 800 ml water/100 g, straw, and after 24 hr neutralized with HCl and left for a further 24 hr before being offered to castrated male sheep (wethers) in a maintenance diet containing 35% concentrates. Organic-matter digestibility of straw significantly increased, by 8 and 11 percentage units respectively, after treatment with 200 ml solution containing 4·5 and 9·0 g NaOH. Volume of solution did not affect digestibility.3. In Experiment 2, straw treated as in Experiment 1 was given ad libitum. The highest intake was for straw treated with 200 ml solution containing 4·5 g NaOH/100 g straw, treatment with 9·0 g NaOH giving a significantly lower intake but higher than that of untreated straw.4. In Experiment 3, the in vitro digestibility of milled straw, treated as in Experiments 1 and 4, increased with increasing volumes of solution up to 120 ml/100 g straw, but the response to successive increments of NaOH declined progressively.5. In Experiment 4 chopped straw was mixed with 4·5, 6·75 or 9·0 g NaOH in 30, 60 or 120 ml water/100 g straw and offered as in Experiment 1. Treatments significantly increased straw digestibility, by 8 to 16 percentage units. Increasing the volume of water from 30 to 60 ml significantly improved digestibility, by 5 percentage units at the two lower levels of NaOH. The response to an increase in the level of NaOH was less, and inconsistent. In vitro and in vivo digestibilities were significantly correlated, but it is concluded that the in vitro technique used overestimates the digestibility of treated straw.

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