Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 8 de 8
Filter
Add more filters










Database
Language
Publication year range
1.
J Ayub Med Coll Abbottabad ; 35(4): 670-674, 2023.
Article in English | MEDLINE | ID: mdl-38406958

ABSTRACT

BACKGROUND: Due to its lack of bony support, the shoulder joint has the broadest range of motion out of all the joints in the body. Instead, one of the joints that dislocate most frequently is the shoulder joint. Multiple pathologic abnormalities, including the traumatic separation of the anterior-inferior capsule-labral complex from the glenoid rim, are caused by repeated anterior glenohumeral dislocation. The objective of the study is to ascertain the Bristow-LATARJET procedure's efficacy in situations of recurrent post-traumatic anterior shoulder instability. METHODS: From 31 January 2020 to 31 July 2020, a descriptive case series was undertaken in the orthopaedic surgery department of the Lahore General Hospital. For this study, 71 patients who met the inclusion and exclusion criteria were recruited, and all interventions were conducted while the patients were lying in a beach chair while under general anaesthesia. The Delto-pectoral incision surgical technique was applied. For 12 weeks, all patients underwent clinical follow-up, and the results were documented. RESULTS: There were 50(70.4%) males and 21(29.6%) females in this study & the mean age of the patients were 34.64±10.73. There were 37(52.1%) patients among them the outcome of treatment (Rowe Scale at 12th week) was excellent, among 21(29.6%) it was good, among 8(11.3%) it was fair and among 5 (7.0%) it was poor. There was a significant association between the outcome of treatment (Rowe scale at 12th week) and age groups (p-value: 0.000). CONCLUSIONS: The Bristow-LATARJET procedure is deemed to be a very productive, safe, and problem-free procedure for curing post-traumatic reoccurring traumatic anterior shoulder instability.


Subject(s)
Joint Instability , Shoulder Dislocation , Shoulder Joint , Male , Female , Humans , Shoulder Joint/surgery , Joint Instability/etiology , Joint Instability/surgery , Shoulder , Shoulder Dislocation/etiology , Shoulder Dislocation/surgery , Range of Motion, Articular , Recurrence , Retrospective Studies
2.
Bioengineered ; 12(1): 2603-2615, 2021 12.
Article in English | MEDLINE | ID: mdl-34115572

ABSTRACT

The hippocampus plays a key role in memory formation and learning. According to the concept of active systems memory consolidation, transiently stored memory traces are transferred from the hippocampus into the neocortex for permanent storage. This phenomenon relies on hippocampal network oscillations, particularly sharp wave ripples [SPW-Rs). In this process prior saved data in the hippocampus may be reactivated. Recent investigations reveal that several neurotransmitters and neuromodulators including norepinephrine, acetylcholine, serotonin, etc., suppress SPW-Rs activity in rodents' hippocampal slices. This suppression of SPW-Rs may depend on various presynaptic and postsynaptic parameters including decrease in calcium influx, hyperpolarization/depolarization and alteration in gap junctions' function in pyramidal cells. In this study, we demonstrate the impact of calcium influx and gap junctions on pyramidal cells for the modulation of SPW-Rs in a computational model of CA1.We used,SPW-Rs model with some modifications. SPW-Rs are simulated with gradual reduction of calcium and with decreasing conductance through gap junctions in PCs. Both, with calcium reduction as well as with conductance reduction through gap junctions, SPW-Rs are suppressed. Both effects add up synergistically in combination.


Subject(s)
Action Potentials/physiology , Calcium/metabolism , Computer Simulation , Gap Junctions/metabolism , Pyramidal Cells/physiology , Axons/physiology , Dendrites/physiology , Interneurons/physiology , Models, Neurological , Synapses/physiology
3.
Pak J Pharm Sci ; 32(6): 2659-2665, 2019 Nov.
Article in English | MEDLINE | ID: mdl-31969299

ABSTRACT

Stress is a state that seriously disturbs psychological or physiological homeostasis of the body and subsequently affects the morphology and function of the hippocampus. Currently available anti-stress medications provide limited benefits with cost of severe adverse effects. In the present study, effect of Rosa moschata extract was evaluated using acute restraint model in mice. The stress suppressant activity of Rosa moschata was evaluated by using elevated plus maze test (EPM), dark light box test and open field test (OFT) following restraint stress protocol. Results showed that the Rosa moschata extract significantly enhanced the number of transitions and the time spent in the open arm in the EPM, increased the number of transitions and time spent in the light compartment of the dark light box, and also enhanced the locomotor activity in OFT, as compared to the stress group. In addition, LD50 of the plant extract is greater than 5000mg/Kg. Thus the findings of our studies show that Rosa moschata significantly alleviates stress following the acute restraint stress in mice. Further studies dealing with underlying mechanism and characterization of active fraction/compound may provide an alternative therapy for stress and related neurological conditions.


Subject(s)
Anti-Anxiety Agents/pharmacology , Plant Extracts/pharmacology , Rosa/chemistry , Stress, Psychological/prevention & control , Animals , Anti-Anxiety Agents/adverse effects , Anti-Anxiety Agents/isolation & purification , Fruit/chemistry , Locomotion/drug effects , Male , Maze Learning/drug effects , Mice , Mice, Inbred BALB C , Phytotherapy , Plant Extracts/adverse effects , Plant Extracts/isolation & purification , Restraint, Physical
4.
Arch Toxicol ; 92(10): 3191-3205, 2018 10.
Article in English | MEDLINE | ID: mdl-30143847

ABSTRACT

Propofol is the most frequently used intravenous anesthetic for induction and maintenance of anesthesia. Propofol acts first and formost as a GABAA-agonist, but effects on other neuronal receptors and voltage-gated ion channels have been described. Besides its direct effect on neurotransmission, propofol-dependent impairment of mitochondrial function in neurons has been suggested to be responsible for neurotoxicity and postoperative brain dysfunction. To clarify the potential neurotoxic effect in more detail, we investigated the effects of propofol on neuronal energy metabolism of hippocampal slices of the stratum pyramidale of area CA3 at different activity states. We combined oxygen-measurements, electrophysiology and flavin adenine dinucleotide (FAD)-imaging with computational modeling to uncover molecular targets in mitochondrial energy metabolism that are directly inhibited by propofol. We found that high concentrations of propofol (100 µM) significantly decrease population spikes, paired pulse ratio, the cerebral metabolic rate of oxygen consumption (CMRO2), frequency and power of gamma oscillations and increase FAD-oxidation. Model-based simulation of mitochondrial FAD redox state at inhibition of different respiratory chain (RC) complexes and the pyruvate-dehydrogenase show that the alterations in FAD-autofluorescence during propofol administration can be explained with a strong direct inhibition of the complex II (cxII) of the RC. While this inhibition may not affect ATP availability under normal conditions, it may have an impact at high energy demand. Our data support the notion that propofol may lead to neurotoxicity and neuronal dysfunction by directly affecting the energy metabolism in neurons.


Subject(s)
CA3 Region, Hippocampal/drug effects , Electron Transport Complex II/antagonists & inhibitors , Neurotoxicity Syndromes/etiology , Propofol/adverse effects , Adenosine Triphosphate/metabolism , Anesthetics, Intravenous/adverse effects , Animals , CA3 Region, Hippocampal/metabolism , Electron Transport Complex II/metabolism , Flavin-Adenine Dinucleotide/metabolism , Hippocampus/drug effects , Hippocampus/metabolism , Male , Mitochondria/drug effects , Mitochondria/metabolism , Organ Culture Techniques , Oxygen Consumption/drug effects , Rats, Wistar , Synaptic Transmission/drug effects
5.
Neurosci Lett ; 574: 15-20, 2014 Jun 27.
Article in English | MEDLINE | ID: mdl-24796812

ABSTRACT

Sharp wave-ripple complexes (SPW-R) are observed in vivo during resting immobility, consummatory behavior and during slow wave sleep, and they have been proposed to support memory consolidation. It has been suggested that GABAergic cells play important roles in controlling incidence of sharp waves and of ripple frequency. We report here that the GABAB agonist baclofen reversibly suppresses SPW-R activity in rat hippocampal slices, presumably affecting the strength of neuronal coupling in the associative network of area CA3. The effect is specific as the GABAB receptor antagonist CGP55846 prevents this effect; however, CGP55846 application had no major effect on incidence of SPW-R. Interestingly, repetitive stimulation in the presence of baclofen is able to induce SPW-R activity, which only appears after washout of baclofen. Our findings suggest that GABA levels through activation of GABAB receptors may be involved in the transition from theta-gamma to SPW-R working mode in the hippocampus.


Subject(s)
Hippocampus/physiology , Receptors, GABA-B/metabolism , Animals , Electric Stimulation , Excitatory Postsynaptic Potentials , GABA-B Receptor Agonists/pharmacology , GABA-B Receptor Antagonists/pharmacology , Hippocampus/drug effects , In Vitro Techniques , Male , Pyramidal Cells/drug effects , Pyramidal Cells/physiology , Rats, Wistar
6.
Nat Prod Res ; 26(5): 484-8, 2012.
Article in English | MEDLINE | ID: mdl-21809956

ABSTRACT

Vitex negundo Linn. (Verbenaceae) is used in traditional medical system for respiratory disorders. This study was carried out to investigate its cough-relieving potential. The antitussive effect of the butanolic extract of V. negundo (Vn) on sulphur dioxide (SO(2))-induced cough was examined in mice. Safety profile of Vn was carried out by observing acute neurotoxicity, median lethal dose (LD(50)) and behavioural signs. Vn dose-dependently (250-1000 mg kg(-1)) inhibited the cough provoked by SO(2) gas in mice and exhibited maximum protection after 60 min of administration. At 1000 mg kg(-1), Vn caused maximum cough-suppressive effects i.e. cough inhibition at 60 min was 67.4%, as compared to codeine (10 mg kg(-1)), dextromethorphan (10 mg kg(-1)) and saline having cough-inhibitory potential 75.7%, 74.7% and 0%, respectively. LD(50) value of V. negundo was found to be greater than 5000 mg kg(-1). In toxicity tests, no signs of neural impairment and acute behavioural toxicity were observed at antitussive doses and extract has been well tolerated at higher doses. These results indicate that V. negundo exhibits antitussive effect and it was found devoid of toxicity.


Subject(s)
Antitussive Agents/therapeutic use , Cough/drug therapy , Plant Extracts/therapeutic use , Vitex/chemistry , Animals , Antitussive Agents/adverse effects , Antitussive Agents/chemistry , Mice , Plant Extracts/adverse effects , Plant Extracts/chemistry
7.
Pharm Biol ; 49(6): 627-32, 2011 Jun.
Article in English | MEDLINE | ID: mdl-21554006

ABSTRACT

CONTEXT: Ballota limbata Benth. (Lamiaceae) (syn, Otostegia limbata Hook.f.) is a species grown in the North West Frontier Province and the lower hills of West Punjab, Pakistan. Ballota species are renowned for their antispasmodic, antiulcer, diuretic, vermifuge, and especially sedative effects. However, little is known about the biological activity of B. limbata. OBJECTIVE: Evaluation of antitussive activity and safety profile of dried B. limbata extract. MATERIALS AND METHODS: Whole air-dried plants were partitioned with various solvents and the butanol fraction was subjected to antitussive evaluation using a sulfur dioxide (SO(2))-induced cough model in mice. Codeine and dextromethorphan were used as positive control. Safety profile of the testing material was established using standard toxicity tests. RESULTS: B. limbata extract inhibited cough provoked by SO(2) gas in mice in a dose-dependent manner. The extract exhibited maximum protection against SO(2)-induced cough after 60 min of administration. B. limbata offered maximum cough suppressive effects, that is, number of coughs during 60 min was 11.66 ± 1.2 (mean ± SEM), after s.c. administration of 800 mg/kg, as compared with codeine 10 mg/kg, s.c., dextromethorphan 10 mg/kg, s.c., and saline showing a frequency of cough of 11.75 ± 1.18, 12.25 ± 0.83, and 46.25 ± 1.52, respectively. LD(50) value of B. limbata was greater than 5000 mg/kg. No sign of neural impairment was observed at antitussive doses and the extract has been well-tolerated at higher doses. DISCUSSION AND CONCLUSION: This study demonstrates that the extract of B. limbata has shown strong cough suppressive effect in mice without yielding any notable toxicity.


Subject(s)
Antitussive Agents/toxicity , Antitussive Agents/therapeutic use , Cough/drug therapy , Phytotherapy/methods , Plant Extracts/toxicity , Plant Extracts/therapeutic use , Animals , Ballota/chemistry , Codeine/therapeutic use , Cough/chemically induced , Dextromethorphan/therapeutic use , Disease Models, Animal , Dose-Response Relationship, Drug , Drug Evaluation, Preclinical , Female , Lethal Dose 50 , Male , Medicine, Traditional , Mice , Mice, Inbred Strains , Pakistan
8.
Hippocampus ; 19(3): 273-88, 2009 Mar.
Article in English | MEDLINE | ID: mdl-19173289

ABSTRACT

Monoamines are implicated in a cognitive processes in a variety of brain regions, including the hippocampal formation, where storage and retrieval of information are facilitated by synchronous network activities. We have investigated the effects of norepinephrine, serotonin, and dopamine on carbachol-, kainate-, and stimulus-induced hippocampal gamma-oscillations employing combined extra- and intracellular recordings. Monoamines dose-dependently and reversibly suppressed kainate- and carbachol-induced gamma-oscillations while increasing the frequency. The effect of serotonin was mimicked by fenfluramine, which releases serotonin from presynaptic terminals. Forskolin also suppressed kainate- and carbachol-induced gamma-oscillations. This effect was mimicked by 8-Br-cAMP and isoproterenol, an agonist of noradrenergic beta-receptor suggesting that the monoamines-mediated suppression of these oscillations could involve intracellular cyclic adenosine 3',5'-cyclic monophosphate (AMP). By contrast, stimulus-induced gamma-oscillations were dose-dependently augmented in power and duration after monoamines application. Intracellular recordings from pyramidal cells revealed that monoamines prolonged the stimulus-induced depolarization and membrane potential oscillations. Stimulus-induced gamma-oscillations were also suppressed by isoproterenol, the D1 agonist SKF-38393 forskolin, and 8-Br-cAMP. This suggests that the augmentation of stimulus-induced gamma-oscillations by monoamines involves--at least in part-different classes of cells than in case of carbachol- and kainate-induced gamma-oscillations.


Subject(s)
Biogenic Monoamines/pharmacology , Hippocampus/drug effects , Hippocampus/physiology , 2,3,4,5-Tetrahydro-7,8-dihydroxy-1-phenyl-1H-3-benzazepine/pharmacology , 8-Bromo Cyclic Adenosine Monophosphate/pharmacology , Animals , Carbachol/pharmacology , Central Nervous System Agents/pharmacology , Colforsin/pharmacology , Dopamine/pharmacology , Electric Stimulation , Fenfluramine/pharmacology , In Vitro Techniques , Isoproterenol/pharmacology , Kainic Acid/pharmacology , Membrane Potentials/drug effects , Norepinephrine/pharmacology , Pyramidal Cells/drug effects , Pyramidal Cells/physiology , Rats , Rats, Wistar , Serotonin/pharmacology , Serotonin Agents/pharmacology
SELECTION OF CITATIONS
SEARCH DETAIL