PROTECTIVE ROLE OF CLOMIPHENE CITRATE FROM THE BIOCHEMICAL EFFECTS OF ATRAZINE EXPOSURE IN ADULT MALE RATS .

2012 ◽  
Vol 11 (2) ◽  
pp. 82-92 ◽  
Author(s):  
M.A. AL-Diwan ◽  
Mohammad R. S. AL-Attabi
2021 ◽  
Author(s):  
Amany Mohamed Shalaby ◽  
Adel Mohamed Aboregela ◽  
Mohamed Ali Alabiad ◽  
Mona Tayssir Sadek

Abstract Diabetes mellitus (DM) represents a widespread metabolic disease with a well-known neurotoxicity in both central and peripheral nervous systems. Oxymatrine is a traditional Chinese herbal medicine that has various pharmacological activities including; anti-oxidant, anti-apoptotic and anti-inflammatory potentials. The present work aimed to study the impact of diabetes mellitus on the cerebellar cortex of adult male albino rat and to evaluate the potential protective role of oxymatrine using different histological methods. Fifty-five adult male rats were randomly divided into three groups: group I served as control, group II was given oxymatrine (80 mg/kg/day) orally for 8 weeks and group III was given a single dose of streptozotocin (50mg/kg) intaperitoneally to induce diabetes. Then diabetic rats were subdivided into two subgroups: subgroup IIIa that received no additional treatment and subgroup IIIb that received oxymatrine similar to group II. The diabetic group revealed numerous changes in the Purkinje cell layer in the form of multilayer arrangement of Purkinje cells, shrunken cells with deeply stained nuclei as well as focal loss of the Purkinje cells. A significant increment in GFAP and synaptophysin expression was reported. Transmission electron microscopy showed irregularity and splitting of myelin sheaths in the molecular layer, dark shrunken Purkinje cells with ill-defined nuclei, dilated Golgi saccules and dense granule cells with irregular nuclear outlines in the granular layer. In contrast, these changes were less evident in diabetic rats that received oxymatrine. In conclusion, Oxymatrine could protect the cerebellar cortex against changes induced by DM.


2012 ◽  
Vol 26 (12) ◽  
pp. 522-532 ◽  
Author(s):  
Suganya Sekaran ◽  
Selvakumar Kandaswamy ◽  
Krishnamoorthy Gunasekaran ◽  
Elumalai Perumal ◽  
Fariya Yasmine Afsar Basha ◽  
...  

2012 ◽  
Vol 36 (0E) ◽  
pp. 172-181
Author(s):  
Baraa N. AL-Okaily

This study was designed to investigate the effect of sodium nitrate as oxidant agent on hepatic function of adult male rats, as well as the possible protective role of vitamin E and flavonoid extracted from Nigella Sativa seeds against the deleterious effects of sodium nitrate. Forty adult male rats were randomly divided in to 4 equal groups and treated daily for 84 days as follows: Animals in the first group were received normal saline, serving as control (group C), rats of the second group (T1) were intubated orally sodium nitrate 30mg/kg. B.W.; animals in T2 group were intubated orally vit. E 40mg/Kg B.W. in addition to sodium nitrate, while rats in the fourth group (T3) were intubated orally 50mg/kg B.W of flavonoids was extracted from Nigella Sativa seeds with sodium nitrate. Blood samples were collected at 0, 21, 42, 63 and 84 days of experiment to study the following parameters: Serum alanine aminotransferase (ALT) and alkaline phosphtase activity (ALP), serum billirubin, as well as hemoglobin concentration. The result revealed that oral intubation of 30mg/kg. B.W of sodium nitrate (T1 group) for 84 days caused hepatic damage manifested by significant increase (p<0.05) in serum ALT and ALP activities, bilirubin concentration and depression in hemoglobin concentration. On other hand, the protective role of vitamin E and flavonoids extracted from Nigella Sativa was clarified in groupsT2 and T3, including correction of hepatic damage manifested by significant (p<0.05) depression in ALT and ALP activities and bilirubin concentration as well as significant (p<0.05) elevation in hemoglobin concentration. In conclusion, the results of this study confirm the protective role of vitamin E and flavonoids of Nigella sativa seed against hepatic dysfunction caused by sodium nitrate manifested by structural and functional changes.


2019 ◽  
Vol 26 (28) ◽  
pp. 28940-28950 ◽  
Author(s):  
Samuel Gbadebo Olukole ◽  
Damilare Olaniyi Lanipekun ◽  
Eunice Olufunke Ola-Davies ◽  
Bankole Olusiji Oke

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