The possible histo-toxicological impacts of long-term dietary supplementation of Soybean and Canola oil on liver in Swiss albino mice

Author(s):  
Md Sharif ◽  
Ziaul Haque ◽  
Md Islam
2002 ◽  
Vol 22 (6) ◽  
pp. 393-402 ◽  
Author(s):  
B. Tunca ◽  
U. Egeli ◽  
N. Aydemir ◽  
G. Cecener ◽  
R. Bilaloglu

2012 ◽  
Vol 3 (1) ◽  
pp. 87-91 ◽  
Author(s):  
MAQ Miah ◽  
MA Awal ◽  
MM Rahman ◽  
MS Islam

The effects of long-term intramuscular injection of gentamicin (Gentin® inj., Opsonin, Bangladesh Ltd.) were studied clinicopathologically on twenty 60 day-old Swiss Albino mice of either sex for 42 days during January to March 2002. All the mice were grouped into four, each consisting of one male and four female mice, of which one group (group A) served as control without giving any treatment while groups B, C and D received recommended (50 mg / kg), medium (75 mg / kg) and double the recommended (100 mg / kg) doses of gentamicin intramuscularly daily for 42 days. All the treated mice produced mild to severe clinical signs, i.e., roughness of the body coat, dullness, depression, anorexia and weakness. At recommended and medium doses the offspring were apparently normal but at double the recommended dose, 10% offspring were died and others were weak and emaciated. No significant gross change was found in lungs, spleen and heart of all the treated groups but the kidney was found soft, flabby and enlarged and the heart was found darker, congested with necrotic foci on the surface. Histopathological changes showed chronic interstitial nephritis in groups B and C following recommended (50 mg / kg) and medium (75 mg / kg) doses while severe glomerulonephritis was observed following double the recommended dose (100 mg / kg) of gentamicin. In liver, histopathological study showed coagulation necrosis following recommended dose, whereas, karyorrhoexis and tissue regeneration were found following medium and double the recommended doses. In lungs, haemorrhage and thickening of interstitial tissues were observed following double the recommended dose of gentamicin in mice. Thus long term administration of higher dose of gentamicin is detrimental to the vital organs.


2011 ◽  
Vol 3 (8) ◽  
pp. 680-684 ◽  
Author(s):  
Faiza Rifat ◽  
◽  
Archana Sharma ◽  
Preeti Srivastava ◽  
Shikha Patni ◽  
...  

2016 ◽  
Vol 72 (9) ◽  
Author(s):  
Dr. Ayman Salah El-Seedy ◽  
Hany George Shalaby ◽  
Mohamed Ahmed El-Sehrigy ◽  
Madiha Mohiy El-Dein Ghoneim

Author(s):  
D.T. Fefar ◽  
Ankita N. Brahmbhatt ◽  
B.P. Joshi ◽  
D.J. Ghodasara

A study was conducted on 5 weeks old 64 (32 male and 32 female) Swiss albino mice to assess the haemato-biochemical and immunological effects of acetamiprid. All the male and female mice were randomly divided into eight different groups. The groups I (male) and II (female) served as controls whereas remaining groups served as treatment groups and were administered acetamiprid at the daily dose rate of 20, 10, 5 mg/kg body weight in males(Group III, V, VII) and females (Group IV, VI,VIII),respectively for 28 days. After 28 days treatment, blood samples were collected for hematological, biochemical as well as immunological analysis. There was significant decrease in haematological parameters like Hb, TEC, TLC, neutrophils and lymphocytes count in high dose groups and revealed potential adversity of acetamiprid at rates of 20 mg/kg/day on haematopoetic system of mice. A dose dependent significant rise in mean values of AST and ALT was observed in treatment groups, whereas there was significant decrease in total protein and albumin and increase in BUN in high and mid dose treated groups, irrespective of sex of mice. Dinitroflurobenzene (DNFB) test conducted to assess the cell mediated immunity revealed the toxic effect of acetamiprid on cell mediated immunity of mice at dose level of 10 mg/kg/day. The mice of high dose group revealed a significant decrease in HA titer and indicated the immunotoxic potential of acetamiprid at dose level of 20 mg/kg/day.


Biologia ◽  
2019 ◽  
Vol 75 (1) ◽  
pp. 139-149
Author(s):  
Venkatesh Bommalapura Kulkarni ◽  
Raghu Ram Achar ◽  
Maheshwari Mahadevappa ◽  
Dinesh Sosalagere Manjegowda ◽  
Priya Babu Shubha ◽  
...  

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