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1.
J Matern Fetal Neonatal Med ; 33(5): 718-725, 2020 Mar.
Article in English | MEDLINE | ID: mdl-30189756

ABSTRACT

Aim: Propylthiouracil (PTU) is frequently used as an antithyroid medication. It is also commonly used to induce hypothyroidism in rodents. PTU administration and hypothyroidism have been shown to affect the liver function. Nigella sativa (NS) has been suggested to have antioxidant and hepatoprotective effects. The objective of this study was to investigate the effects of NS extract administration during neonatal and juvenile growth period on liver function of PTU-induced hypothyroid rats.Methods: The pregnant rats were kept in separate cages. After delivery, the mothers and their offspring were randomly divided into five groups and were treated with the following programs: (1) control; (2) PTU, 0.005% in their drinking water (3-5); PTU-plus 100, 200, or 400 mg/kg NS extract. After lactation period, the offspring continued to receive the same experimental treatment for the first 8 weeks of their life. Ten offspring of each group were randomly selected and weighted at days 10, 30, and 60 after delivery. Their blood samples were collected and the liver tissues were removed.Results: Malondialdehyde (MDA) concentration was increased while, thiol concentration and superoxide dismutase (SOD) and catalase (CAT) activity were decreased in the liver tissues of PTU-treated rats. Serum aspartate amino transferase (AST), alkaline phosphatase (ALK-P), and alanine aminotransferase (ALT) levels in the PTU group were higher than the control group. Treatment with 200 and 400 mg/kg decreased MDA while increasing thiol concentration in the liver tissues compared to the PTU group. Treatment with all doses of the extract decreased serum ALK-P concentration compared with the PTU group. Treatment with 400 mg/kg NS increased CAT and SOD concentrations in the liver tissues and decreased serum AST and ALT concentrations compared to the PTU group. PTU decreased body weight gain of offspring and while, the extract increased the body weight gain of offspring rats.Conclusion: The results of this study demonstrated that administration of NS hydroalcoholic extract in the neonatal and juvenile growth period has an improving effect on the liver function of PTU- induced hypothyroid rats.


Subject(s)
Hypothyroidism/drug therapy , Liver/drug effects , Nigella sativa , Phytotherapy , Plant Extracts/therapeutic use , Animals , Animals, Newborn , Drug Evaluation, Preclinical , Female , Hypothyroidism/chemically induced , Plant Extracts/pharmacology , Pregnancy , Propylthiouracil , Rats, Wistar
2.
Drug Chem Toxicol ; 42(2): 167-175, 2019 Mar.
Article in English | MEDLINE | ID: mdl-29745257

ABSTRACT

This study was conducted to investigate protective effects of Urtica dioica extract on acetylcholinesterase (AChE) activity and the oxidative damage of brain tissues in scopolamine-induced memory impairment model. The rats were treated with (1) saline (control), (2) scopolamine, and (3-5) the plant extract (20, 50, or 100 mg/kg) before scopolamine. The traveled distance and the latency to find the platform in Morris water maze (MWM) by scopolamine-treated group were longer while the time spent in target quadrant was shorter than those of the control. Scopolamine decreased the latency to enter the dark in passive avoidance test. Besides, it also increased AChE activity and malondialdehyde (MDA) concentration in the hippocampal and cortical tissues while decreased thiols content and superoxide dismutase (SOD) and catalase (CAT) activities in the brain (p < 0.01-p <0.001). Treatment by the extract reversed all the effects of scopolamine (p < 0.05-p <0.001). According to the results of present study, the beneficial effects of U. dioica on memory can be attributed to its protective effects on oxidative damage of brain tissue and AChE activity.


Subject(s)
Acetylcholinesterase/drug effects , Memory Disorders/drug therapy , Oxidative Stress/drug effects , Plant Extracts/pharmacology , Scopolamine/pharmacology , Urtica dioica/chemistry , Acetylcholinesterase/metabolism , Animals , Brain Chemistry/drug effects , Cerebral Cortex/chemistry , Cerebral Cortex/drug effects , Cerebral Cortex/enzymology , Hippocampus/chemistry , Hippocampus/drug effects , Hippocampus/enzymology , Male , Malondialdehyde/analysis , Maze Learning/drug effects , Memory Disorders/chemically induced , Neuroprotective Agents/pharmacology , Rats , Rats, Wistar , Superoxide Dismutase/metabolism
3.
Metab Brain Dis ; 32(2): 617-628, 2017 04.
Article in English | MEDLINE | ID: mdl-28078553

ABSTRACT

Diabetes during pregnancy impairs the development of the central nervous system (CNS) and causes cognitive and behavioral abnormalities in offspring. However, the exact mechanism by which the maternal diabetes affects the development of the brain remains to be elucidated. The aim of the present study was to investigate the effects of maternal diabetes in pregnancy on the expression of Bcl-2 and Bax genes and the numerical density of degenerating dark neurons (DNs) in the hippocampus of offspring at the first postnatal two weeks. Wistar female rats were maintained diabetic from a week before pregnancy through parturition and male offspring was sacrificed at P0, P7, and P14. Our findings demonstrated a significant down-regulation in the hippocampal expression of Bcl-2 in the diabetic group newborns (P < 0.05). In contrast, the mRNA expression of Bax was markedly up-regulated in the offspring born to diabetic dams at all of studied time-points (P < 0.05). Moreover, we found a striking increase in the numerical density of DNs in the various subfields of hippocampus of diabetic group pups (P < 0.05). The results of the present study revealed that maternal hyperglycemia during gestational period may result in disturbances in the expression of Bcl-2 and Bax genes as two important genes in neuronal apoptosis regulation and induces the production of DNs in the developing hippocampus of neonatal rats. These disturbances may be a reason for the cognitive, structural, and behavioral anomalies observed in offspring born to diabetic mothers. Furthermore, the control of maternal glycaemia by insulin administration in most cases normalized these negative impacts.


Subject(s)
Animals, Newborn/metabolism , Apoptosis Regulatory Proteins/biosynthesis , Apoptosis Regulatory Proteins/genetics , Diabetes Mellitus, Experimental/genetics , Diabetes Mellitus, Experimental/pathology , Diabetes, Gestational/genetics , Diabetes, Gestational/pathology , Hippocampus/metabolism , Hippocampus/pathology , Animals , Blood Glucose/metabolism , Female , Gene Expression Regulation , Genes, bcl-2 , Neurons/metabolism , Neurons/pathology , Pregnancy , Prenatal Exposure Delayed Effects , Rats , Rats, Wistar , bcl-2-Associated X Protein/biosynthesis , bcl-2-Associated X Protein/genetics
4.
Drug Chem Toxicol ; 40(2): 206-214, 2017 Apr.
Article in English | MEDLINE | ID: mdl-27387089

ABSTRACT

OBJECTIVE: The neuroprotective effects of both garlic and ascorbic acid (AA) have been documented. In this study the effects of garlic and ascorbic acid on memory deficits and brain tissue oxidative damages induced by lead exposure was investigated. METHODS: The juvenile rats were divided and treated: (1) Control, (2) Lead (lead acetate in drinking water, 8 weeks), (3) Lead - Ascorbic Acid (Lead-AA), (4) Lead - Garlic (100 mg/kg, daily, gavage) (Lead-Gar). RESULTS: In Morris water maze (MWM), the escape latency and traveled path in the Lead group were significantly higher while, the time spent in the target quadrant (Q1) was lower than Control. Both Lead-Gar and Lead-AA groups spent more times in Q1than to lead group. There were no significant differences in swimming speed between the groups. In passive avoidance (PA) test, the time latency for entering the dark compartment by Lead group was lower than Control. Treatment of the animals by AA and garlic significantly increased the time latency. In Lead group, the total thiol concentration in brain tissues was significantly lower while, MDA was higher than Control. Treatment by both garlic and AA increased total thiol concentrations and decreased MDA. Both garlic and AA decreased the lead content of brain tissues. CONCLUSION: It is suggested that treatment with garlic attenuates the learning and memory impairments due to lead exposure during juvenile rat growth which is comparable to AA. The possible mechanism may be due to its protective effects against brain tissues oxidative damage as well the lowering effects of brain lead content.


Subject(s)
Antioxidants/pharmacology , Ascorbic Acid/pharmacology , Behavior, Animal/drug effects , Brain/drug effects , Garlic , Lead Poisoning, Nervous System, Childhood/drug therapy , Memory Disorders/drug therapy , Memory/drug effects , Neuroprotective Agents/pharmacology , Nootropic Agents/pharmacology , Plant Extracts/pharmacology , Age Factors , Animals , Brain/metabolism , Brain/pathology , Brain/physiopathology , Disease Models, Animal , Escape Reaction/drug effects , Garlic/chemistry , Lead Poisoning, Nervous System, Childhood/pathology , Lead Poisoning, Nervous System, Childhood/physiopathology , Lead Poisoning, Nervous System, Childhood/psychology , Male , Malondialdehyde/metabolism , Maze Learning/drug effects , Memory Disorders/pathology , Memory Disorders/physiopathology , Memory Disorders/psychology , Neuroprotective Agents/isolation & purification , Nootropic Agents/isolation & purification , Organometallic Compounds , Oxidative Stress/drug effects , Phytotherapy , Plant Extracts/isolation & purification , Plant Roots , Plants, Medicinal , Rats, Wistar , Reaction Time , Sulfhydryl Compounds/metabolism , Time Factors
5.
Nutr Neurosci ; 20(1): 49-59, 2017 Jan.
Article in English | MEDLINE | ID: mdl-25087773

ABSTRACT

OBJECTIVES: It has been shown that hypothyroidism-induced oxidative damage in brain tissue is involved in its adverse effects on learning and memory. Nigella sativa (N. sativa) has been suggested to have antioxidant and neuroprotective effects. The objective of this study was to investigate the effects of hydroalcoholic extract of N. sativa on hypothyroidism-associated learning and memory impairment during neonatal and juvenile growth in rats. METHODS: Thirty pregnant rats were kept in separate cages. After delivery, the mothers and their offspring were randomly divided into six groups including: (1) control, (2) PTU (propylthiouracil), (3) PTU-NS 100, (4) PTU-NS 200, (5) PTU-NS 400, and (6) PTU-Vit C (vitamin C). All dams except the control group received 0.005% PTU in their drinking water during lactation. Besides PTU, dams in groups 3, 4, 5, and 6 received 100, 200, and 400 mg/kg N. sativa extract, or 100 mg/kg Vit C, respectively. After lactation period, pups continued to receive same experimental treatment for the first 8 weeks of their life. Then, 10 male offspring of each group were randomly selected and assessed for the learning and memory abilities by using Morris water maze (MWM) and passive avoidance (PA) tests. Blood samples were collected for thyroxine assessment, animals were euthanized, and the brain tissues were removed and analyzed for total thiol groups and malondialdehyde (MDA) concentrations. RESULTS: PTU exposure significantly increased the time latency in MWM test, while reduced the time spent in target quadrant, and decreased the latency for entering the dark compartment in PA test. These effects were associated with significant reduction in serum thyroxine levels and brain levels of thiol groups, and significant elevation in hippocampal MDA. Administration of 400 mg/kg N. sativa extract and 100 mg/kg Vit C reduced the time latency, while increased the time spent in target quadrant compared to the PTU group in MWM test. Treatment by 100-400 mg/kg of N. sativa extract and also Vit C significantly increased the time latency for entering the dark compartment in PA test. The serum thyroxine concentrations of the animals treated by all doses of the N. sativa extract as well as by Vit C were higher than that of the PTU group. Two hundred and four hundred milligrams/kilogram of NS extract and 100 mg/kg Vit C decreased the MDA concentration in hippocampal tissues, while increased thiol contents compared to the PTU group. DISCUSSION: The results of this study demonstrate that the hydroalcoholic extract of N. sativa have protective effects on hypothyroidism-associated learning and memory impairment during neonatal and juvenile growth in rats. The effects were comparable to Vit C and might be due to the protective effects of N. sativa extract against brain tissues' oxidative damage.


Subject(s)
Dietary Supplements , Disease Models, Animal , Learning Disabilities/prevention & control , Memory Disorders/prevention & control , Nigella sativa/chemistry , Nootropic Agents/therapeutic use , Plant Extracts/therapeutic use , Animals , Animals, Newborn , Antioxidants/administration & dosage , Antioxidants/therapeutic use , Behavior, Animal , Cerebral Cortex/metabolism , Cerebral Cortex/pathology , Ethnopharmacology , Hippocampus/metabolism , Hippocampus/pathology , Hypothyroidism/metabolism , Hypothyroidism/pathology , Hypothyroidism/physiopathology , Learning Disabilities/etiology , Lipid Peroxidation , Male , Medicine, Traditional , Memory Disorders/etiology , Neurons/metabolism , Neurons/pathology , Nootropic Agents/administration & dosage , Oxidative Stress , Plant Extracts/administration & dosage , Random Allocation , Rats, Wistar
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