Effect of phytohemagglutinin on bone marrow protection and recovery in rodents

1969 ◽  
Vol 47 (7) ◽  
pp. 587-590
Author(s):  
I. H. Plenderleith

Attempts were made to prevent the hematologic and general toxic effects of radiation, cyclophosphamide, and 6-mereaptopurine in various animal species by giving erythrocyte-absorbed phytohemagglutinin intravenously prior to or following such treatment. A single dose of total body radiation was used in the radiation studies, with mice receiving 800 and rats 600 rads. Cyclophosphamide was given to mice intraperitoneally in a dose of 0.25 mg/g of body weight on two occasions 6 days apart. 6-Mercaptopurine was given to other groups of mice intraperitoneally in a dose of 0.25 mg/g of body weight daily for 11 days and to rabbits subcutaneously in a dose of 0.01 to 0.015 mg/g of body weight daily for 14 days. No evidence of a protective effect or of enhanced recovery could be demonstrated in any of the animals treated with erythrocyte-absorbed phytohemagglutinin as compared with animals not so treated.

2007 ◽  
Vol 23 (9) ◽  
pp. 453-462 ◽  
Author(s):  
Ming-Yii Huang ◽  
Shi-Long Lian ◽  
Hsin-Lung Wu ◽  
Chee-Yin Chai ◽  
Shun-Jen Chang ◽  
...  

1982 ◽  
Vol 68 (4) ◽  
pp. 277-282 ◽  
Author(s):  
G. Bogliolo ◽  
G. Massa ◽  
A. Sobrero ◽  
I. Pannacciulli

The alleged possibility that testosterone propionate (TP) has a protective effect on hemopoietic cells submitted to the damaging effect of antitumoral drugs was studied. The bone marrow content and the proliferating fraction of CFUs were determined following a single dose of 450 mg/kg of TP. At selected times after TP injection (2 and 4 days), TP-treated mice received a single dose of azathioprine, hydroxyurea, vinblastine, cyclophosphamide, BCNU and doxorubicin. The bone marrow CFUs were determined 24 h after drug administration. The CFUs-surviving fraction in all cases appeared similar to or lower than that found in controls not treated with TP. It seems therefore that in this experimental setting TP does not reduce the toxic effect of anticancer drugs on hemopoietic pluripotent stem cells. However, this finding does not exclude a possible protective effect of TP at different levels of hemopoiesis or when the steroid is administered with a different schedule.


1988 ◽  
Vol 66 (5) ◽  
pp. 663-665 ◽  
Author(s):  
Ethel L. B. Novelli ◽  
Ney L. Rodrigues ◽  
Bartolomé O. Ribas

The potential of nickel chloride to prevent streptozotocin-induced hyperglycemia was tested in rats in vivo. To induce diabetes, streptozotocin (100 mg/kg body weight) was injected as a single dose. Streptozotocin treatment resulted in a significant decrease in plasma insulin and ceruloplasmin, and pancreatic Cu, protein, and Cu–Zn superoxide dismutase activity. In rats treated with nickel chloride (10 mg/kg body weight) and streptozotocin, these values were comparable with those observed in control rats. The results indicate that nickel chloride injected before streptozotocin prevented streptozotocin-induced hyperglycemia, and suggest that the protective effect was related to Cu–Zn superoxide dismutase activity, mediated by copper.


1986 ◽  
Vol 4 (S1) ◽  
pp. 219-224 ◽  
Author(s):  
W.B. Rybka ◽  
S. Caplan ◽  
C.R. Freeman ◽  
P. Koch ◽  
S. Lehnert ◽  
...  

2001 ◽  
Vol 45 (12) ◽  
pp. 3555-3559 ◽  
Author(s):  
K. C. Carter ◽  
A. B. Mullen ◽  
S. Sundar ◽  
R. T. Kenney

ABSTRACT In this study, the in vitro and in vivo efficacies of free sodium stibogluconate (SSG) and a nonionic surfactant vesicular formulation of SSG (SSG-NIV) against a laboratory strain ofLeishmania donovani (MHOM/ET/67:LV82) and different clinical isolates of L. donovani were determined. Treatment with SSG-NIV was more effective against intramacrophage amastigotes than treatment with SSG. In vivo murine studies showed that there was interstrain variability in the infectivity of the different L. donovani strains, with two of the strains (20001 and 20003) giving low parasite burdens. In addition, interstrain variability in the antileishmanial efficacy of SSG in a single dose containing 300 mg of Sb(V)/kg of body weight was observed. This dose of free drug either caused a >97% reduction in liver parasite burdens or had no significant effect on parasite burdens compared with the result with the respective control. In some instances, treatment with this free SSG dose also caused a significant reduction in spleen (strain 20006) or bone marrow (strains 20001 and 20009) parasite burdens. Treatment with SSG-NIV was more effective than that with SSG against all of the strains tested. In SSG-responsive strains, the reduction in liver parasite burdens by SSG-NIV treatment was similar to that caused by free SSG. In SSG-nonresponsive strains, SSG-NIV treatment caused at least a 95% reduction in liver parasite burdens. Overall, these results indicate that the use of a vesicular formulation of SSG is likely to increase its clinical efficacy against visceral leishmaniasis.


Author(s):  
Asha P. Dass ◽  
Prashanth Chary Ramoji

Background: This study was aimed at investigating the effects of aluminium chloride (AlCl3) in altering the serum lipid profiles and ways to reduce its effect using two different doses of ginger extract 500mg/kg and 1000mg/kg body weight in male wister rats.Methods: The rats were randomly divided into 4 groups consisting of 5 animals in each group. Groups II, III and IV received AlCl3 100mg/kg bodyweight single dose, Groups III and IV receiving an additional daily oral single dose of ginger plant extract through a stomach tube. All animals were fasted before the treatment. All rats were weighed before the start of the experiment and at the end of the experiment. The blood was collected firstly at the beginning of the experiment, then on the 45th day. The collected blood was left to clot then centrifuged at 3500 rpm for 5 min. The serum was separated and stored at - 80°C for later analyses.Results: This study shows that a single dose of 100mg/kg aluminium chloride causes a rise in total body weight, TC (total cholesterol), LDL (low density lipoproteins) and TG (triglycerides) levels in the rat, and aqueous Zingiber officinal (ginger) extract reduces this rise in TC, LDL and TG levels in the rats.Conclusions: Ginger was effective in lowering serum cholesterol levels levels in the ginger treated rats to almost normal value. These results indicate that treatment with aqueous extract of ginger may be effective in lowering lipid levels in AlCl3 induced hyperlipidemia in rats.


1999 ◽  
Vol 36 (1-3) ◽  
pp. 1-36 ◽  
Author(s):  
Jeffrey M. Levengood ◽  
Glen C. Sanderson ◽  
William L. Anderson ◽  
George L. Foley ◽  
Loretta M. Skowron ◽  
...  

We conducted a 30-day acute toxicity test of zinc (Zn) shot using 6- to 8-month-old wild-type game-farm Mallards (Anas platyrhynchos), 40 of which (20 males and 20 females) were dosed with 6 No. 4 candidate shot pellets containing 98% Zn and 2% tin (Sn); the remaining 40 ducks were dosed with 6 No. 4 steel (Fe) shot and served as controls. The Zn shot resulted in high mortality, with a greater proportion of females dying than males. For the 30-day study, survival averaged 18 and 23 days for female and male Zn-dosed ducks, respectively; all Fe-dosed ducks survived to Day 30. Ataxia/paresis and other signs of intoxication were noted in a large portion of Zn-dosed ducks. For all ducks retaining 6 shot pellets, including those that survived < 30 days, shot retention, percent of the original shot weight dissolved, and dissolution rates were similar for Zn- and Fe-dosed ducks. For those ducks that retained 6 pellets and survived to Day 30, percent loss of the original shot weight and the dissolution rate were higher in Zn-dosed ducks. Mean body weight in Zn-dosed ducks decreased between Days and 15, and between Days 15 and 30 in Zn-dosed females. Zn-intoxicated ducks lost a considerable proportion of their body weight between dosing and death. The kidneys of Zn-dosed ducks as a group were heavier, and the pancreases, livers, and gizzards lighter, as compared with Fe-dosed ducks. The liver (males) and kidneys of Zn-dosed ducks that died as a result of Zn intoxication were heavier, whereas thegonads (females) and gizzards were lighter, as compared with those that survived. The liver, pancreas, and kidneys increased, whereas the gonads (males) and gizzards decreased, as a proportion of total body weight in Zn-dosed ducks that died prior to Day 30. Mean packed cell volume (PCV) decreased between Days and 15 and increased between Days 15 and 30 in male and female Zn-dosed ducks. PCV values changed little in Fe-dosed ducks over the course of the study; however, PCV decreased dramatically in Zn-intoxicated ducks. A variety of gross lesions was observed, most often associated with the gastrointestinal tract. Grossly, cecal lesions were the most consistent and dramatic changes observed. No macroscopic lesions were observed in the Fe-dosed ducks, and histologic lesions in this group were considered within normal limits for game-farm ducks. Histologic lesions observed in Zn-dosed Mallards most often included pancreatic apoptosis, splenic lymphoid depletion and/or lympholysis, necrohemorrhagic typhlitis, and necrosis of the epithelial cells of the renal tubules. We detected high concentrations of Zn, and alterations in levels of other elements, in the tissues of Zn-dosed ducks relative to Fe-dosed controls. Mean Zn concentrations were greater in Zn-dosed ducks for all tissues examined, and levels in the kidneys, livers, and pancreases of Zn-intoxicated Mallards were similar to levels associated with toxic effects reported in other studies. Mean tissue tin (Sn) concentrations were below the Method Detection Limit (MDL) in all cases; few individual Sn values were above MDLs. Changes in tissue element concentrations tended to be more dramatic in ducks that died as a result of Zn intoxication than in Zn-dosed ducks that survived the experiment. Gender differences in analyte concentrations were detected for some tissues. These results indicated that dosing of 6- to 8-month-old game-farm Mallards with 6 No. 4 shot comprised of 98% Zn and 2% Sn produced toxic effects under the test conditions.


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