Arsenic-induced histopathology and synthesis of stress proteins in liver and kidney of Channa punctatus

2006 ◽  
Vol 65 (2) ◽  
pp. 218-229 ◽  
Author(s):  
Sonali Roy ◽  
Shelley Bhattacharya
1993 ◽  
Vol 134 ◽  
pp. 641-645
Author(s):  
Probodh Ghosh ◽  
Shampa Ghosh ◽  
Shambhunath Bose ◽  
Shelley Bhattacharya

2016 ◽  
Vol 2 (3) ◽  
pp. 464-470
Author(s):  
Gias Uddin Ahmed ◽  
Sahara Khatun ◽  
Md Mamunur Rahman

Investigation on the health condition of small indigenous fish, Channa punctatus was carried out through clinical and histological observation from Jailka beel of Sherpur sadar, Sherpur district and Kailla beel of Ishargonj upazila, Mymensingh district for a period of six months from October 2014 to March 2015. Water quality parameters like water temperature, pH, dissolved oxygen, ammonia, total hardness, alkalinity and nitrate were recorded. Water temperature and total hardness were found at unfavorable level for fish in December and January. Clinical examinations of the fish were also carried out for any kind of abnormalities at monthly intervals. Clinically, it was observed that fish was affected with numerous red spots and patches in lateral and ventral regions, large deep whitish ulcers reached up to deep ulcers especially in December and January in both the beels. Samples of skin, muscle, gill, liver and kidney were collected and processed for histological observations. Major pathology in the skin and muscle were epidermis separated from dermis, presence of fungal granuloma, vacuums, hemorrhage and necrosis. Loss of primary and secondary gill lamellae, hypertrophy and primary gill lamellae separated, necrosis and hemorrhage were found in the gill. Large vacuums, necrosis and hemorrhage were observed in liver and kidney. Among the affected fish organs, skin and muscle, gills were found to be more affected than those of the internal organs like liver and kidney. Overall, under the clinical and histopathological observations the fish were found to be more affected in December and January. Whereas, in the months of February and March, the pathological condition of fish gradually healed up to normal except few vacuums and hemorrhage. Under histopathological observations, fish of Jailka beel were more affected than the fish of Kailla beel. In clinical and histopathological observation C. punctatus was more affected due to EUS.Asian J. Med. Biol. Res. September 2016, 2(3): 464-470


1995 ◽  
Vol 73 (1) ◽  
pp. 153-158 ◽  
Author(s):  
Arnulfo Albores ◽  
Christopher J. Sinal ◽  
John R. Bend ◽  
M. George Cherian

Arsenic is a known pulmonary, hepatic, and skin carcinogen in humans and a known inducer of stress proteins. Consequently, the ability of arsenite (As3+) to modulate isozyme-selective cytochrome P450 (P450) dependent monooxygenase activities was investigated in microsomes prepared from lung, liver, and kidney of male, adult Sprague–Dawley rats treated subcutaneously (s.c.) with sodium arsenite (75 μmol/kg body weight) 24 h before death. In the lung, the activity of P450 1A1 catalyzed 7-ethoxyresorufin O-deethylation (ERFD) was markedly (approximately 5-fold) increased in treated versus control rats, whereas the activity of P450 2B catalyzed 7-pentoxyresorufin O-depentylation (PRFD) was unchanged. Pulmonary ERF activity remained elevated for at least 48 h after As3+ treatment. In contrast, As3+ inhibited hepatic microsomal ERFD and PRFD activity by approximately 20 and 35%, respectively, 24 h after treatment. ERFD activity was also decreased in kidney microsomes of As3+-treated rats, but the inhibition was greater than in liver (50 vs. 35%) 24 h after injection. These effects are almost certainly not due to a direct action of As3+ on P450-dependent catalysis, as in vitro addition of sodium As3+ at concentrations up to 1 mM had no effect on ERFD activity of control rat lung microsomes. In addition, pretreatment of rats with Zn (153 μmol∙kg−1∙day−1 for 2 days, s.c.) had no effect on control or As3+-mediated changes in P450-dependent ERFD activity of rat lung or kidney microsomes. These results demonstrate that As3+ is an isozyme-selective modulator of P450 monooxygenase activity (i.e., significant increase of P450 1A1 catalyzed activity but not P450 2B catalyzed activity) in rat lung. In contrast, ERFD activity was significantly inhibited in both liver and kidney of the same As3+-treated rats.Key words: microsomal cytochrome P450, arsenite, oxidative stress, induction, liver, lung, kidney, monooxygenase activity.


2021 ◽  
Author(s):  
Sunil P. Trivedi ◽  
Shefalee Singh ◽  
Abha Trivedi ◽  
Manoj Kumar

Abstract The current study was strived to investigate the adverse effects of Mercuric chloride (HgCl2) overload in the fish Channa punctatus. Two sub-lethal test concentrations of HgCl2 viz., 1/20th and 1/10th of 96 h LC50 i.e., 0.03 mg/L and 0.07 mg/L, respectively, were used for exposure. Blood, liver and kidney tissues of the control and exposed specimens were sampled at intervals of 15, 30 and 45 days to assess alterations in oxidative stress, genotoxicity haematological parameters and histopathology. Significant changes in Hb%, RBC count, WBC count, antioxidant enzyme activity viz., super oxide dismutase (SOD), catalase (CAT), glutathione (GSH) and glutathione reductase (GR) were recorded. Micronuclei (MN) induction, nuclear abnormalities (NA) and histopathological alterations were also observed in the exposed fish. Significant (p < 0.05) increase in activities of SOD, CAT, GSH, GR and after 45 d decrease in the level of GSH and GR suggest an undermined anti-oxidative defence system in the fish exposed to HgCl2. Histological examination of liver and kidney showed serious tissue injury and histological alterations. Significant increase in MN and NA frequencies reveal the DNA damage in erythrocytes of fish and haematological changes show the toxicological potential of HgCl2. The observed genotoxicity, biochemical, haematological and histological changes in the present study provide the most extensive insight of HgCl2 stress in Channa punctatus.


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