scholarly journals BONE MARROW OF NORMAL GUINEA PIGS

Blood ◽  
1948 ◽  
Vol 3 (9) ◽  
pp. 1050-1054 ◽  
Author(s):  
ARTHUR SAWITSKY ◽  
LEO M. MEYER

Abstract 1. A method is presented describing the technic for obtaining bone marrow from the iliac crest of the guinea pig by aspiration. 2. The cellular constituents in the peripheral blood and bone marrow of normal guinea pigs are presented. 3. Peripheral blood and bone marrow findings in guinea pigs are compared with those of other observers and with other animal species where the aspiration technic was used.

Author(s):  
Corazon D. Bucana

In the circulating blood of man and guinea pigs, glycogen occurs primarily in polymorphonuclear neutrophils and platelets. The amount of glycogen in neutrophils increases with time after the cells leave the bone marrow, and the distribution of glycogen in neutrophils changes from an apparently random distribution to large clumps when these cells move out of the circulation to the site of inflammation in the peritoneal cavity. The objective of this study was to further investigate changes in glycogen content and distribution in neutrophils. I chose an intradermal site because it allows study of neutrophils at various stages of extravasation.Initially, osmium ferrocyanide and osmium ferricyanide were used to fix glycogen in the neutrophils for ultrastructural studies. My findings confirmed previous reports that showed that glycogen is well preserved by both these fixatives and that osmium ferricyanide protects glycogen from solubilization by uranyl acetate.I found that osmium ferrocyanide similarly protected glycogen. My studies showed, however, that the electron density of mitochondria and other cytoplasmic organelles was lower in samples fixed with osmium ferrocyanide than in samples fixed with osmium ferricyanide.


1976 ◽  
Vol 36 (02) ◽  
pp. 401-410 ◽  
Author(s):  
Buichi Fujttani ◽  
Toshimichi Tsuboi ◽  
Kazuko Takeno ◽  
Kouichi Yoshida ◽  
Masanao Shimizu

SummaryThe differences among human, rabbit and guinea-pig platelet adhesiveness as for inhibitions by adenosine, dipyridamole, chlorpromazine and acetylsalicylic acid are described, and the influence of measurement conditions on platelet adhesiveness is also reported. Platelet adhesiveness of human and animal species decreased with an increase of heparin concentrations and an increase of flow rate of blood passing through a glass bead column. Human and rabbit platelet adhesiveness was inhibited in vitro by adenosine, dipyridamole and chlorpromazine, but not by acetylsalicylic acid. On the other hand, guinea-pig platelet adhesiveness was inhibited by the four drugs including acetylsalicylic acid. In in vivo study, adenosine, dipyridamole and chlorpromazine inhibited platelet adhesiveness in rabbits and guinea-pigs. Acetylsalicylic acid showed the inhibitory effect in guinea-pigs, but not in rabbits.


Blood ◽  
1949 ◽  
Vol 4 (3) ◽  
pp. 217-246 ◽  
Author(s):  
MAX SAMTER

Abstract 1. The eosinophilic response of the guinea pig sensitized and reinjected with the specific antigen varies with the nature of the antigen used, but also with the individual guinea pig in any groupsensitized and reinjected with the same antigen. 2. Certain antihistamine drugs which abolish anaphylactic symptoms, do not abolish the eosinophilic response. 3. The severity of anaphylactic "shock" symptoms has no influence on the eosinophilic response. 4. Histamine phosphate has no effect on the eosinophil count of nonsensitized guinea pigs protected by benadryl; it causes a distinct eosinophilic response in sensitized animals. 5. Heparin—in the dose injected—produced only an insignificant rise in the peripheral eosinophil count of sensitized guinea pigs; adenosine had no effect. 6. Attempts were made to correlate the eosinophilic response in bone marrow, blood and shock tissue of guinea pigs sensitized and reinjected with a specific antigen. The variation within a wide range of the number of eosinophils in the bone marrow of nonsensitized and of sensitized, reinjected guinea pigs is emphasized. A definite correlation seems to exist between the presence of a large number of eosinophils in blood and lungs; it is shown, however, that this observation permits only limited conclusions. 7. The factors which account for discrepancies in the interpretation of the eosinophilic response, e.g., nature of antigen, route of administration and characteristics of species, are analyzed. 8. The significance of the findings is reviewed in the light of previous work.


Blood ◽  
1965 ◽  
Vol 25 (5) ◽  
pp. 693-702 ◽  
Author(s):  
THEODORE I. MALININ ◽  
VERNON P. PERRY ◽  
CAREY C. KERBY ◽  
MICHAEL F. DOLAN

Abstract Homologous peripheral blood leukocytes were injected into lethally irradiated guinea pigs. Histologic examination of these showed a rapid recovery of the bone marrow and the lymphatic tissue following an injection of a sufficient number of leukocytes. All control animals died with a hypoplastic bone marrow. Protected animals did not develop "secondary" disease during 9 months of observation.


Blood ◽  
1971 ◽  
Vol 38 (3) ◽  
pp. 372-377 ◽  
Author(s):  
CORNELIUS ROSSE

Abstract Guinea pigs were given 14 daily injections of 3H-thymidine to label a proportion of cells with a slow rate of turnover in addition to rapidly proliferating cells. In the bone marrow the only unlabeled cells were some reticular, endothelial, and plasma cells, damaged cells, and 14.1% of small lymphocytes. Six weeks after discontinuation of 3H-thymidine 7% of the marrow lymphocytes remained labeled. In guinea pigs injected every 4 hr with 3H-thymidine for 4 days to label all cells entering DNA synthesis, 14.4% of small lymphocytes remained unlabeled along with some reticular, endothelial, phagocytic, monocytoid, damaged, and plasma cells. The pattern of appearance of labeled lymphocytes was consistent with the kinetics of transitional cells that function as their precursors. Thus, in the bone marrow of the guinea pig the majority of lymphocytes have a short lifespan and a rapid turnover, whereas about 14% turn over more slowly and 7% have a life-span exceeding 4 wk. In this respect the kinetics of marrow lymphocyte production differs from that of the rat.


1993 ◽  
Vol 4 (1) ◽  
pp. 19-25 ◽  
Author(s):  
J. S. Feng ◽  
J. Y. Crouch ◽  
P. Y. Tian ◽  
H. L. Lucia ◽  
G. D. Hsiung

The antiviral effects of ganciclovir (DHPG) combined with zidovudine (AZT) at several dosages against cytomegalovirus infection were evaluated in cultured cells and in Hartley guinea pigs. Combinations of DHPG and AZT at fixed ratios ranging from 1:0.1 to 1:1 showed reduced antiviral effects of DHPG in cultured human lung fibroblast (HEL) cells and guinea pig embryo (GPE) cells infected with human cytomegalovirus and guinea pig cytomegalovirus, respectively. Synergistic cytotoxicity (CI values < 1) was noted in HEL and GPE cell cultures at all DHPG/AZT combinations tested. In vivo experiments using a fixed ratio at three dosage levels for treatment of GPCMV infected guinea pigs for 5 days did not show significant antagonistic antiviral nor synergistic toxic effects at lower dosages. When GPCMV infected guinea pigs were treated with DHPG and AZT in combinations at 40/20, 40/40 and 40/80 mg kg−1 day 1 for 7 days, a significant increase of GPCMV infectivity titres in the salivary gland, lung and spleen were noted when compared with those animals treated with DHPG 40mg kg−1 day−1 alone. In addition, histopathological findings showed more cytotoxicity in the bone marrow of infected and non-infected animals treated wth DHPG/AZT combinations than animals treated with each drug alone. These results suggest that AZT antagonizes the antiviral effects of DHPG against HCMV and GPCMV replication in cultured cells and GPCMV infection in guinea pigs with increased cytotoxicity in cultured cells and in bone marrow of animals receiving the drug combinations.


1967 ◽  
Vol 18 (03/04) ◽  
pp. 686-690
Author(s):  
Y Modai ◽  
R Oren ◽  
A de Vries ◽  
A Kohn

SummaryIntraperitoneal infection of guinea pigs with Encephalomyocarditis (EMC) virus led to viremia 2-10 days after infection and to paralysis and death of some of the infected animals. During the course of infection there was marked leucocytosis and thrombocytopenia. No abnormalities were detected in megakaryocytes in bone marrow cultures from infected guinea pigs. Exposure of guinea pig bone marrow culture to EMC virus in vitro impaired granulation and disintegration of megakaryocytes to platelets.


1963 ◽  
Vol 118 (5) ◽  
pp. 727-742 ◽  
Author(s):  
Jacob Fong ◽  
Dennis Chin ◽  
Herta M. Vickrey

Immunization of mice or guinea pigs with BCG rendered all or most of the histiocytes of these animals resistant to necrotization by virulent H37Rv; this cellular resistance was mediated by immune serum. Immune mouse histiocytes (from BCG-immunized animals) were able to induce cellular resistance in normal homologous and heterologous (rabbit) animal species; mouse histiocytic ribosomes were also tested in the homologous species and found to be active. Immune guinea pig histiocytes (from BCG-immunized guinea pigs) were ineffective in transferring cellular resistance to either homologous or heterologous (mouse and rabbit) animal species. Immune rabbit histiocytes were capable of inducing cellular resistance in mice and guinea pigs; rabbit histiocytic ribosomes were also tested in normal mice and found to be active in induction of cellular resistance. Recipient guinea pig histiocytes (from guinea pigs inoculated with immune rabbit histiocytes) were capable of inducing cellular resistance in normal guinea pigs and rabbits. Cultivation of lysed immune histiocytes of all three animal species on glycerol-blood agar medium failed to reveal any viable BCG; this provided one additional bit of evidence against the idea that induction of cellular resistance is due to viable bacilli.


1917 ◽  
Vol 25 (1) ◽  
pp. 45-64 ◽  
Author(s):  
Kikutaro Ishiwara ◽  
Toyoitsiro Ohtawara ◽  
Kotaro Tamura

1. We have confirmed Ogata's results in experimental rat-bite fever caused by the bite of rats. 2. In our experiments with guinea pigs, swelling and congestion of the bitten parts, swelling of the subcutaneous lymph nodes, fever, and loss of weight were the typical symptoms. The progress of the fever was not so regular as in human cases, but we find records in the literature of patients who showed irregular fever types or were afebrile. The chief points that we noted in the anatomical view of the guinea pigs were swelling and congestion of the lymph gland system and acute changes in the adrenals and kidneys. 3. If an emulsion made from the lymph glands, cerebral substance, or the adrenals, or the heart's blood of a guinea pig of the original generation is inoculated subcutaneously or intraperitoneally into a fresh guinea pig, the animal invariably dies with the usual symptoms of fever and swelling of the lymph glands. The anatomical changes in this case were the same as those of the original guinea pig, except that the course was shorter and more regular. The same result was observed in further generations. No change was observed in pathogenicity, and in the guinea pigs of the original and further generations a species of spirochete as the causative agent was always observed. The incubation period in the original generation was from 1 to 2 weeks, and in further generations about 1 week. 4. When a mouse or white rat was inoculated, spirochetes always appeared in the peripheral blood, but no other symptoms developed. When peripheral blood drawn from a mouse thus treated was inoculated into a fresh mouse or a fresh white rat and peripheral blood drawn from the mouse and rat was inoculated into a fresh guinea pig, they all became infected and the guinea pigs always died. Thus we found that rats and mice are media but not victims of the disease, while guinea pigs are both media and victims of it. 5. In the rhesus monkey on which we made our experiment we witnessed a process similar to that of human rat-bite fever, and our spirochotes were observed in other animals into which blood drawn from the monkey was inoculated. 6. In the original animals spirochetes were seen chiefly toward the end of the process and the conditions as to the period previous to it are not yet clearly known. In further generations of all the animals we used, spirochetes were found in the peripheral blood 4 or 5 days after inoculation, and gradually multiplied until the greates number was reached about the 10th day after inoculation. They then began to decrease; yet spirochetes could be observed over 2 months later. 7. We have found spirochetes chiefly in the adrenals of the animals by Levaditi's method, but have not yet ascertained their distribution in other organs. 8. Our spirochete is short, round, and highly motile; it stains readily, and has few spirals. We have not yet observed an undulating membrane, but have seen what we believe to be flagellum at each end. 9. The identification of our spirochete with other species must be left for further study. The spirochete which Futaki, Takaki, Taniguchi, and Osumi found in two patients with rat-bite fever, seems to differ from ours in form. 10. Spirochetes disappear from the blood of the animals as a result of the injection of salvarsan, thus indicating that the spirochete is arsentropic.


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