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1.
Pak J Pharm Sci ; 33(6(Supplementary)): 2831-2836, 2020 Nov.
Article in English | MEDLINE | ID: mdl-33879444

ABSTRACT

For centuries, herbs and herbal oils are used for pharmacological purpose. Aloe vera is well-known as silent healer and flax seed oil is known to contain rich amount of omega-3 fatty acids, both are having effects on central nervous system. Valproic acid is anticonvulsant drug with some side effects and has shown effects on behaviors. This study was designed to monitor the effects of valproic acid, aloe vera and flax seed oil on cognitive and anxiolytic behaviors in rats. Animals were categorized into four groups: Control, valproic acid, aloe vera and flax seed oil which were respectively treated with water, valproic acid (300mg/kg), aloe vera (0.4ml/kg) and flax seed oil (1.8ml/kg). The treatment was continued 2 weeks for drug and 3 weeks for aloe vera and flax seed oil. Anxiolytic effect as well as increased GABA levels were observed following drug and oil treatments. Improvement in cognitive function with decrease in acetylcholine esterase activity in aloe vera and flax seed oil while impairment in learning memory with increase acetylcholine esterase activity was observed in rats treated with valproic acid. Results showed substantial decrease in acetylcholinesterase level in aloe vera and flax seed oil supporting the cognitive impact of oils in contrary to drug.


Subject(s)
Aloe , Anti-Anxiety Agents/pharmacology , Linseed Oil/pharmacology , Memory/drug effects , Valproic Acid/pharmacology , Animals , Rats , Rats, Wistar , gamma-Aminobutyric Acid/analysis
2.
Pak J Pharm Sci ; 31(6 (Supplementary): 2639-2644, 2018 Nov.
Article in English | MEDLINE | ID: mdl-30587473

ABSTRACT

Essential oils are natural products having several important chemical constituents. Traditionally used worldwide as natural alternatives for treating various pathological conditions due to their antibacterial, anti-inflammatory, antifungal and antioxidants properties. Citral is one of the mono terpene present in lemon peel oil. The present study aimed to evaluate the effects of citral at low (0.1 mg/kg) and high (1 mg/kg) doses. In this study rats were subjected to different behavioral parameters such as tail suspension test (TST) to monitor depressive behavior, open field test (OFT) for locomotor activity, light/dark transition test (LDT) for the assessment of level of anxiety and the strength of muscles were monitored by Kondziela's inverted screen test. Plasma corticosterone and antioxidant enzymes activities were also estimated. The results from the present study showed that citral at 0.1mg/kg dose significantly increased the mobility time in TST, increased number of square crossed in OFT, increased time spent in LDT and showed muscles strengthen activity in Kondziela's inverted screen test. Lipid per oxidation (LPO) was decreased and antioxidant profile was improved along with the decrease in plasma corticosterone following the administration of 0.1mg/kg dose of citral in rats. However, at a high dose of 1 mg/kg of citral, behavioral alterations were observed along with the increased plasma corticosterone and decreased activities of antioxidant enzymes in rats. Therefore present findings suggested that citral at low dose has therapeutic potential as compared to high dose. It can be used as an alternative therapy for the treatment of various ailments in humans and animals.


Subject(s)
Antioxidants/pharmacology , Locomotion/drug effects , Monoterpenes/pharmacology , Oxidative Stress/drug effects , Plant Oils/pharmacology , Acyclic Monoterpenes , Animals , Dose-Response Relationship, Drug , Drug Administration Schedule , Locomotion/physiology , Oils, Volatile/pharmacology , Oxidation-Reduction , Oxidative Stress/physiology , Rats , Rats, Sprague-Dawley
3.
Pak J Pharm Sci ; 31(4(Supplementary)): 1603-1608, 2018 Jul.
Article in English | MEDLINE | ID: mdl-30058555

ABSTRACT

Stress has become an integral feature of everyday living. Each individual that lives encounters some manifestation of stress in life. Stress causes certain alterations in the structure and functions of the body and is considered to be a major factor in many health problems. Many synthetic and natural compounds are used for the attenuation of stress induced changes in the body. Medicinal plants are used since ancient times to prevent from neurological disorders. Lavender (Lavandula angustifolia) is very efficacious and possesses the ability to improve several neurological disorders. Nonsteroidal anti-inflammatory drugs (NSAIDs) are commonly used against pain and inflammation. However, effectiveness of NSAIDs in the treatment of various psychiatric ailments is also reported. The present study investigated the effects of ibuprofen and lavender oil on stress induced behavioral and biochemical alterations in rats. The rats were subjected to restraint stress and behavioral parameters like open field test (OFT), light/dark transition box activity (LDT) and forced swim test (FST) were used to assess exploratory, anxiolytic and anti-depressant activity, respectively. Corticosterone, lipid peroxidation (LPO) and endogenous antioxidant enzymes activities were also estimated. Results of OFT, LDT and FST showed substantial effects of lavender oil and standard drug ibuprofen. A significant decrease in plasma corticosterone and LPO levels with increase in antioxidant enzyme activities was observed in the study. However, the effects of lavender oil were more as compared to standard drug ibuprofen in diminution of stress induced behavioral and biochemical changes in rats. This study demonstrates that lavender oil is more remedial than ibuprofen in stress related disorders.


Subject(s)
Anti-Inflammatory Agents, Non-Steroidal/therapeutic use , Antioxidants/therapeutic use , Ibuprofen/therapeutic use , Lipid Peroxidation/drug effects , Oils, Volatile/therapeutic use , Plant Oils/therapeutic use , Stress, Psychological/drug therapy , Animals , Anti-Anxiety Agents/pharmacology , Anti-Anxiety Agents/therapeutic use , Anti-Inflammatory Agents, Non-Steroidal/pharmacology , Antioxidants/pharmacology , Corticosterone/antagonists & inhibitors , Corticosterone/blood , Ibuprofen/pharmacology , Lavandula , Lipid Peroxidation/physiology , Oils, Volatile/pharmacology , Plant Oils/pharmacology , Rats , Stress, Psychological/blood , Stress, Psychological/psychology
4.
Neuroscience ; 370: 121-129, 2018 02 01.
Article in English | MEDLINE | ID: mdl-29141189

ABSTRACT

Memory functions can be considerably affected by various life events and stress has shown to be a chief regulator. Different stress patterns have distinct effects on the overall functioning of the brain. Stress provokes inflammation not only in the periphery but also in the brain. Neuroinflammation causes alterations in neuronal structure and function, which eventually progress to the development of neurodegenerative diseases. Inflammatory reactions are modulated through communication between the nervous, endocrine and immune systems. An excessive release of stress hormones and changes in the neurotransmission system may cause cognitive impairments. The present study investigated dissimilar stress-related memory deficits and their diminution by non-steroidal anti-inflammatory drugs (NSAIDs). Treatment with cyclooxygenase inhibitors, which inhibit prostaglandin synthesis, has enhanced memory functions in a number of neuroinflammatory states. In this study, rats were exposed to a series of dissimilar stressors and behavioral parameters for depression and memory functions were examined. Corticosterone, serotonin (5-HT) and dopamine (DA) levels were also estimated. Results from the forced swim test, elevated plus maze test and Morris water maze test showed significant effects of NSAIDs. A significant decrease in plasma corticosterone and increased DA and 5-HT levels were observed in NSAID-treated dissimilar-stressed rats. This study demonstrates the therapeutic potential of NSAIDs for dissimilar stress-induced depressive behaviors and impaired memory functions and related hormonal and neurochemical changes in the rat brain.


Subject(s)
Anti-Inflammatory Agents, Non-Steroidal/pharmacology , Cyclooxygenase Inhibitors/pharmacology , Depression/drug therapy , Memory Disorders/drug therapy , Psychotropic Drugs/pharmacology , Stress, Psychological/drug therapy , Animals , Biogenic Monoamines/metabolism , Brain/drug effects , Brain/metabolism , Corticosterone/blood , Depression/etiology , Depression/metabolism , Male , Maze Learning/drug effects , Maze Learning/physiology , Memory Disorders/etiology , Memory Disorders/metabolism , Memory, Long-Term/drug effects , Memory, Long-Term/physiology , Memory, Short-Term/drug effects , Memory, Short-Term/physiology , Random Allocation , Rats, Sprague-Dawley , Stress, Psychological/metabolism
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