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1.
Eur Neuropsychopharmacol ; 16(4): 260-7, 2006 May.
Article in English | MEDLINE | ID: mdl-16168627

ABSTRACT

Stress has been shown to be associated with altered homeostasis that may lead to oxidant-antioxidant imbalance. Non-enzymatic antioxidants are important regulators of reactive oxygen species produced in extra-cellular milieu and represent the first line of defense against them. Extra-cellular non-enzymatic antioxidants may be disturbed by the production of superoxide and nitric oxide and this has not been studied in stressful situation previously. In the present study, effects of immobilization stress (IS), both acute (IS x 1) and repeated (IS x 7) were assessed on extra-cellular total antioxidant capacity measured as plasma ferric reducing antioxidant power (FRAP) and protein sulfhydryls, and oxidative stress measured as leukocyte superoxide generation, plasma nitric oxide production (total nitrates and nitrites, NOx) and lipid peroxides in rats. Effects of pretreatment with nitric oxide synthase (NOS) inhibitors and vitamin E were also studied on these biochemical parameters. The results showed that both IS x 1 and IS x 7 resulted in extra-cellular oxidant-antioxidant imbalance as oxidant generation was increased and non-enzymatic antioxidants were depleted. Pretreatment either with NOS inhibitors or vitamin E restored stress-induced extracellular oxidant-antioxidant imbalance implying their potential role as antioxidants. Our data suggest that there is extra-cellular oxidant-antioxidant imbalance in the stressed rats, with greater magnitude of severity in repeated stress paradigm. Augmentation of antioxidant defenses might be beneficial in long-term stress.


Subject(s)
Antioxidants/therapeutic use , Enzyme Inhibitors/therapeutic use , NG-Nitroarginine Methyl Ester/therapeutic use , Oxidative Stress/drug effects , Stress, Physiological/drug therapy , Vitamin E/therapeutic use , Analysis of Variance , Animals , Antioxidants/metabolism , Behavior, Animal/drug effects , Guanidines/administration & dosage , Leukocytes/metabolism , Lipid Peroxides/metabolism , Male , Nitrates/blood , Nitrites/blood , Oxidation-Reduction , Rats , Rats, Wistar , Restraint, Physical , Stress, Physiological/physiopathology , Superoxides/metabolism , Time Factors
2.
J Ethnopharmacol ; 101(1-3): 299-307, 2005 Oct 03.
Article in English | MEDLINE | ID: mdl-15970412

ABSTRACT

Korean ginseng tea (KGT), prepared from the roots of Panax ginseng, is widely used by Korean people for antistress, antifatigue, and endurance promoting effects. In the present study we evaluated neuroprotective/cerebroprotective actions of KGT in stroke, using rat global and focal models of ischemia. Varied biochemical/enzymatic alterations, produced subsequent to the application of middle cerebral artery (MCAO) and bilateral carotid artery occlusion (BCAO) followed by reperfusion viz. increase in lipid peroxidation (LPO) and decrease in glutathione (GSH), glutathione reductase (GR), catalase (CAT), glutathione-S-transferase (GST), glutathione peroxidase (GPx) and superoxide dismutase (SOD), were markedly reversed and restored to near normal levels in the groups pre-treated with KGT (350 mg/kg given orally for 10 days). It is concluded that the protective action, exhibited by KGT against hypoperfusion/reperfusion induced brain injury, suggests its therapeutic potential in cerebrovascular diseases (CVD) including stroke. These findings are important because: (a) the present treatment strategies for CVD are far from adequate and (b) KGT with wide usage is known to be a safe natural product.


Subject(s)
Brain Ischemia/drug therapy , Neuroprotective Agents/therapeutic use , Panax , Phytotherapy , Plant Extracts/therapeutic use , Animals , Antioxidants/therapeutic use , Brain Ischemia/pathology , Disease Models, Animal , Korea , Male , Rats
3.
Basic Clin Pharmacol Toxicol ; 96(6): 469-74, 2005 Jun.
Article in English | MEDLINE | ID: mdl-15910411

ABSTRACT

Problems associated with mental health have increased tremendously in modern times. The search for effective and safe alternatives should, therefore, be pursued vigorously. Forced immobilization is one of the best explored models of stress in rats and the role of corticosterone, serotonin (5-HT) and catecholamines, i.e. norepinephrine, epinephrine, dopamine is well documented. We investigated the therapeutic potential of two gold preparations (Ayurvedic Swarna Bhasma and Unani Kushta Tila Kalan) in restraint induced stress at different time points of 1 hr, 2 hr and 4 hr. We pretreated rats with two gold preparations, Ayurvedic Swarna Bhasma and Unani Kushta Tila Kalan (25 mg/kg, orally for 10 days) prior to restraint stress. Brain catecholamine, serotonin and plasma corticosterone levels were determined following 1, 2 and 4 hr restraint stress, using HPLC and also plasma corticosterone using luminescence spectrophotometry. Gold preparations restored restraint stress-induced elevation in levels of brain catecholamines (norepinephrine, epinephrine and dopmine), 5-HT and plasma corticosterone to near normal levels. Gold, widely used in modern medicine for the treatment of rheumatoid arthritis, is highly valued for various medicinal uses in Indian systems of medicine. Traditional gold preparations are attributed with tonic/rejuvenating and antioxidant properties. Our earlier studies revealed interesting analgesic, immunostimulant, adaptogenic and glycogen sparing properties in these preparations, but their effects in stress and depression have not been investigated yet. Significant restoration of altered values to near normal levels suggest potentials for gold preparations in stress and depression.


Subject(s)
Brain/drug effects , Gold/therapeutic use , Latex/therapeutic use , Stress, Physiological/metabolism , Animals , Arsenic , Brain/metabolism , Calotropis , Corticosterone/blood , Corticosterone/metabolism , Dopamine/metabolism , Drug Combinations , Epinephrine/metabolism , India , Lead , Male , Medicine, Ayurvedic , Norepinephrine/metabolism , Rats , Rats, Wistar , Serotonin/metabolism , Stress, Physiological/drug therapy
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