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1.
Int J Clin Exp Pathol ; 14(10): 1048-1055, 2021.
Article in English | MEDLINE | ID: mdl-34760041

ABSTRACT

In recent times, there has been an increased risk of human exposure to cadmium especially in developing countries. We studied the role of progesterone as an anti-inflammatory and antioxidant agent in cadmium induced toxicity. Cadmium toxicity was induced with cadmium chloride (30 mg/kg) per oral while the control group was given distilled water. The Cd group was given CdCl2 only, P4 group; progesterone only (10 mg/kg intraperitoneally) and Cd+P4 group; CdCl2 and progesterone. All treatments lasted for 21 days. Following sacrifice, liver function tests and antioxidant status were assessed using standard kits; TNFα was immunolocalized across the study groups and the staining intensity measured using Image J software. Cadmium administration induced oxidative stress by a significant elevation in MDA and GC6P levels and a significant reduction in SOD, CAT, and GSH. These were attenuated by progesterone administration. While cadmium exposure caused an increase in serum ALT, AST, and ALP activities, progesterone significantly alleviated these effects. Inflammation shown by significant immunoreactivity in the TNFα positive cells in the liver in the cadmium group was reversed by progesterone. We conclude that cadmium toxicity induces oxidative stress that was attenuated by progesterone.

2.
Ann Diagn Pathol ; 48: 151604, 2020 Oct.
Article in English | MEDLINE | ID: mdl-32877832

ABSTRACT

The visualization of glycogen deposits in cells and tissues is important for studying glycogen metabolism as well as diagnosis of glycogen storage diseases. Evidence suggests that the demonstration of glycogen can better be enhanced by factors such the choice of fixative and temperature during fixation. Here, we assessed efficacy of neutral buffered formalin (NBF), alcoholic formalin (AF) and paraformaldehyde (PFA) at 4 °C, 37 °C and 40 °C using Periodic Acid Schiff's staining method. Each liver specimen was fixed in NBF and AF while the brain tissues were fixed in NBF, AF and PFA. We found that there was a better PAS staining intensity with the liver tissues fixed in AF compared with NBF. Also, there was no difference in the quality of the staining for tissues fixed in AF at 37 °C, 4 °C and 40 °C, but fixation with NBF at 4 °C gave the best staining quality when compared with 40 °C and 37 °C. Furthermore, hippocampal tissues fixed in AF showed better quality of PAS staining compared with NBF and PFA. A significant increase in staining intensity was observed for PFA when compared with NBF. Superior staining intensity for PAS was observed at 4 °C for hippocampal tissues fixed with NBF, AF and PFA. Taken together our results show that AF at a temperature of 4 °C gave the best result. Hence, glycogen demonstration can better be enhanced by the choice of fixative and temperature during fixation.


Subject(s)
Brain/drug effects , Fixatives/pharmacology , Glycogen/metabolism , Liver/drug effects , Animals , Brain/metabolism , Formaldehyde/pharmacology , Glycogen Storage Disease/diagnosis , Liver/metabolism , Male , Periodic Acid-Schiff Reaction/statistics & numerical data , Photomicrography/methods , Polymers/pharmacology , Rats , Rats, Wistar , Staining and Labeling/statistics & numerical data , Temperature , Tissue Fixation/methods
3.
Afr Health Sci ; 18(2): 253-259, 2018 Jun.
Article in English | MEDLINE | ID: mdl-30602950

ABSTRACT

BACKGROUND: Quinine has been reported to possess anti-spermatogenic activities. OBJECTIVES: This study was carried out to determine the effect of quinine on ovarian function in Sprague-Dawley rats. METHODS: Twenty rats with regular 4-days oestrous cycle divided into 4 groups (N=5) were used. Group I received quinine at 30 mg/kg body weight by gavage for 28 days after which they were sacrificed. The ovaries were excised for biochemical oxidation of glutathione peroxidase (GSH), superoxide dismutase (SOD), catalase and malondialdehyde (MDA). Group II received single dose quinine at 30 mg/kg body weight at 0900 hrs on day of proestrus. Blood was obtained at 1800 hrs for hormonal assay of FSH and LH. The animals were sacrificed the next morning on estrus: oviducts were examined for ova count. Groups III and IV served as controls. RESULTS: Quinine treated rats recorded zero number of ova compared to control. Serum concentration of LH reduced significantly in the quinine treated group compared to the control. Furthermore, quinine significantly decreased the oxidant status of GSH, SOD and catalase and significantly increased MDA levels in the ovary compared to the control group. CONCLUSION: Quinine completely blocks ovulation, suppresses LH surge, and produces oxidative stress in the ovary.


Subject(s)
Estrous Cycle/drug effects , Follicle Stimulating Hormone/blood , Luteinizing Hormone/blood , Ovary/drug effects , Ovulation/drug effects , Oxidative Stress , Quinine/pharmacology , Uterus/drug effects , Animals , Body Weight/drug effects , Catalase/blood , Estrone/blood , Estrous Cycle/blood , Female , Glutathione Peroxidase , Humans , Malondialdehyde/blood , Ovary/pathology , Ovulation/blood , Rats , Rats, Sprague-Dawley , Superoxide Dismutase/blood , Uterus/pathology
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