16 results on '"Toshal R. Patel"'
Search Results
2. Amphiphysin I phosphorylation on residue threonine 260 in a pentylenetetrazole-induced seizure model
- Author
-
Toshal R. Patel, Mowdood Choudhury, James M. Staddon, Oliver Kleiner, Raymond T. Chung, Louise Morgan, and Laura Barden
- Subjects
Threonine ,MAP Kinase Kinase 4 ,Kinase ,General Neuroscience ,Cyclin-dependent kinase 5 ,Nerve Tissue Proteins ,GABA receptor antagonist ,Biology ,Hippocampus ,Synaptic vesicle ,Cell biology ,GABA Antagonists ,Mice ,chemistry.chemical_compound ,chemistry ,Biochemistry ,Seizures ,Amphiphysin ,Animals ,Pentylenetetrazole ,Phosphorylation ,Neurotransmitter - Abstract
A method to evaluate kinase inhibitor action was reported [L. Morgan, S.J. Neame, H. Child, R. Chung, B. Shah, L. Barden, J.M. Staddon, T.R. Patel, Development of a pentylenetetrazole-induced seizure model to evaluate kinase inhibitor efficacy in the central nervous system, Neurosci. Lett. 395 (2006) 143-148]. In this, acute administration of the GABA antagonist pentylenetetrazole triggers seizures through glutamate-dependent pathways. Under such conditions, activation of the c-Jun N-terminal kinase (JNK) pathway was detected in hippocampal extracts. Phosphorylation of the upstream JNK kinase MKK4 was also revealed through use of a phospho-MKK4-specific antibody. Here, this antibody is shown to also react with a protein of approximately 125 kDa which underwent increased phosphorylation in response to pentylenetetrazole treatment. The present study aimed to identify the approximately 125 kDa protein as it may provide novel insight into signalling, neuronal activity and seizures. Using chromatographic methods and mass spectrometry, the protein was identified as amphiphysin I. This was confirmed by 2D gel analysis and immunoblot with amphiphysin I-specific antibodies. Although the phospho-MKK4 antibody was raised against an MKK4-specific peptide, partial sequence homology between this sequence and a region of amphiphysin was discerned. New antibodies raised against the phospho-threonine 260-amphiphysin-specific sequence detected increased phosphorylation in response to pentylenetetrazole treatment. This particular phosphorylation site does not seem to have been described before, possibly reflecting a novel regulatory aspect of amphiphysin biology. As amphiphysin is involved in the regulation of endocytosis, phosphorylation at this site may play a role in the regulated re-uptake of synaptic vesicles after neurotransmitter release.
- Published
- 2008
3. Development of a pentylenetetrazole-induced seizure model to evaluate kinase inhibitor efficacy in the central nervous system
- Author
-
Bina Shah, Laura Barden, Louise Morgan, Toshal R. Patel, Stephen J. Neame, James M. Staddon, Raymond T. Chung, and Hannah Child
- Subjects
Male ,inorganic chemicals ,Cell signaling ,MAP Kinase Kinase 4 ,Proto-Oncogene Proteins c-jun ,Immunoblotting ,Phosphatase ,Convulsants ,macromolecular substances ,Biology ,Mitogen-activated protein kinase kinase ,Hippocampus ,environment and public health ,Neuroprotection ,Mice ,Seizures ,Animals ,Protein phosphorylation ,Phosphorylation ,Protein Kinase Inhibitors ,Kinase ,Activator (genetics) ,General Neuroscience ,Immunohistochemistry ,Cell biology ,Enzyme Activation ,Mice, Inbred C57BL ,Disease Models, Animal ,enzymes and coenzymes (carbohydrates) ,Biochemistry ,Pentylenetetrazole ,bacteria ,Electrophoresis, Polyacrylamide Gel - Abstract
c-Jun N-terminal kinases (JNKs) are implicated in cell death in neurodegenerative disorders. Therefore, JNK inhibitors could act as neuroprotective agents. To evaluate potential candidates, reproducible and quantitative CNS in vivo models are required. To that end, a pentylenetetrazole-induced seizure model was explored. c-Jun phosphorylation was detected in hippocampal extracts by blotting c-Jun immunoprecipitates with phosphorylation-specific antibodies. Pentylenetetrazole administration induced rapid and reproducible increases in c-Jun phosphorylation. However, special attention had to be paid to the composition of the extraction buffer to ensure stabilization of protein phosphorylation, as demonstrated using internal standards of phosphorylated recombinant c-Jun. As JNK and its upstream activator MKK4 are activated by phosphorylation, these events were also evaluated. In principle, kinase inhibitors could act at the level of JNK or upstream kinases to inhibit c-Jun phosphorylation. MKK4 phosphorylation was dramatically increased in response to pentylenetetrazole but, again, only when appropriate phosphatase inhibitors were in the extraction buffer. In contrast, JNK was found to be constitutively phosphorylated and unaltered upon pentylenetetrazole treatment. The JNK inhibitor SP600125 was shown to inhibit c-Jun phosphorylation without affecting MKK4 phosphorylation. Our procedures enable analysis of JNK pathway signalling in a CNS model and, also, should be applicable to that of other protein phosphorylation events in vivo.
- Published
- 2006
4. γ-Secretase modulators: current status and future directions
- Author
-
Adrian, Hall and Toshal R, Patel
- Subjects
Alzheimer Disease ,Imidazoles ,Animals ,Humans ,Amyloid Precursor Protein Secretases - Abstract
This chapter reviews the current status of γ-secretase modulators, highlighting key compounds by each company involved in the area. The review focuses on the three main chemotypes: acids, imidazoles and related derivatives and natural products. A section on chemical biology and ligand-binding site elucidation studies is also included. The primary source of information is drawn from peer reviewed literature as this permits analysis of PK-PD relationships and subsequent comment. Discussion of the patent literature is included for completeness. From this analysis, the key issues and challenges in the area are highlighted. The review concludes with a summary of the clinical development status and comment on future prospects of the field.
- Published
- 2014
5. Endothelin Receptor Antagonist Increases Cerebral Perfusion and Reduces Ischaemic Damage in Feline Focal Cerebral Ischaemia
- Author
-
Hussein Hallak, James McCulloch, Samuel Galbraith, David I. Graham, Annette Marian Doherty, and Toshal R. Patel
- Subjects
Endothelin Receptor Antagonists ,Ischemia ,Dioxoles ,030218 nuclear medicine & medical imaging ,03 medical and health sciences ,0302 clinical medicine ,Bolus (medicine) ,medicine.artery ,medicine ,Animals ,Cerebral perfusion pressure ,Infusions, Intravenous ,business.industry ,Endothelin receptor antagonist ,Endothelins ,medicine.disease ,Arterioles ,Neurology ,Cerebral blood flow ,Ischemic Attack, Transient ,Vasoconstriction ,Cerebrovascular Circulation ,Anesthesia ,Middle cerebral artery ,Cats ,Pia Mater ,Female ,Neurology (clinical) ,medicine.symptom ,Cardiology and Cardiovascular Medicine ,Endothelin receptor ,business ,030217 neurology & neurosurgery - Abstract
These investigations characterised the cerebrovascular effects of an endothelin ETA-receptor antagonist PD156707 in normal and ischaemic cat brain. A dose of PD156707 that inhibited the effects of exogenous endothelin-1 was established in nonischaemic cerebral resistance arterioles. Perivascular microapplication of the endothelin–receptor antagonist PD156707 (0.03–3 μ M) had a minimal effect on nonischaemic pial resistance arterioles. The perivascular coapplication of PD156707 and ET-1 (10 n M) effected a dose-dependent attenuation of the ET-1 vasoconstrictive response (IC50 = 0.1 μ M). Intravenous administration of PD156707 (3 μmol/kg bolus + 5 μmol/kg/h infusion) attenuated the vasoconstriction elicited by perivascular ET-1 (10 n M) in normal pial arterioles (ET-1 vasoconstriction: −37 ± 13% from preinjection baseline; after intravenous PD156707: 6 ± 10% from preinjection baseline). In the focal ischaemia studies, cerebral perfusion was measured in the suprasylvian and ectosylvian gyri (by laser Doppler flowmetry). Occlusion of the middle cerebral artery reduced cerebral perfusion in the suprasylvian and ectosylvian gyri by ∼50%. Intravenous administration of PD156707 (3 μmol/kg bolus + 5 μmol/kg/h infusion), initiated 30 min after middle cerebral artery occlusion, effected a progressive increase in cerebral perfusion up to preocclusion baseline levels, whereas cerebral perfusion in vehicle-treated animals did not vary from its postocclusion level. In these animals, the intravenous administration of PD156707 reduced the hemispheric volume of ischaemic damage by 45% (vehicle: 2,376 ± 1,107 mm3; PD156707: 1,307 ± 548 mm3; p < 0.05). Our investigations indicate that endothelin receptor antagonism may be a new therapeutic strategy for the amelioration of focal ischaemic damage.
- Published
- 1996
6. Endothelin receptor mediated constriction and dilatation in feline cerebral resistance arterioles in vivo
- Author
-
Toshal R. Patel, James McCulloch, and Moira A. McAuley
- Subjects
medicine.hormone ,Agonist ,medicine.medical_specialty ,medicine.drug_class ,Vasodilation ,Biology ,Peptides, Cyclic ,Endothelins ,chemistry.chemical_compound ,Arteriole ,medicine.artery ,Internal medicine ,medicine ,Animals ,Pharmacology ,BQ-123 ,Endothelin-1 ,Receptors, Endothelin ,Brain ,Endothelin 1 ,Peptide Fragments ,Arterioles ,Endocrinology ,chemistry ,Vasoconstriction ,Cerebrovascular Circulation ,Cats ,cardiovascular system ,Female ,Vascular Resistance ,medicine.symptom ,Endothelin receptor - Abstract
The receptors mediating the cerebrovascular actions of endothelins have been examined in feline cerebral resistance arterioles in vivo. The adventitial microapplication of the endothelin ETA receptor antagonist BQ-123 (cyclo D-aspartate-D-tryptophan-L-leucine-D-valine-L-proline) (0.1-10 microM) per se had minimal effect on cerebral resistance arterioles examined. The adventitial microapplication of endothelin-1 (10 nM) elicited a marked vasoconstriction of cerebral resistance arterioles (-29.1 +/- 1.9% from pre-injection baseline). The endothelin-1 induced vasoconstriction was attenuated, in a dose dependent manner, by the adventitial co-application of BQ-123 and endothelin-1 (estimated IC50 0.7 microM). The adventitial microapplication of the endothelin ETB receptor agonist BQ-3020 N-acetyl[Ala11,Ala15]ET-1 (6-21)) (0.001-1 microM) effected a dose dependent vasodilatation (EC50 30 nM, maximum response 25 +/- 5% from pre-injection baseline). The magnitude of the vasodilatation elicited by BQ-3020 (100 nM and 1 microM) was dependent on the pre-injection calibre of the arterioles examined. The intracarotid infusion (via the lingual artery) of BQ-3020 (0.5-500 pmol/min) had no significant effect on the calibre of cerebral resistance arterioles. These results suggest that the peptide endothelin ETB receptor agonist fails to gain access to the cerebrovascular endothelin ETB receptors following its intraluminal administration. These investigations indicate that endothelin ETA receptors mediate vasoconstriction and endothelin ETB receptors mediate vasodilatation in feline cerebral resistance arterioles in vivo.
- Published
- 1996
7. Therapeutic Potential of Endothelin Receptor Antagonists in Cerebrovascular Disease
- Author
-
Toshal R. Patel
- Subjects
medicine.hormone ,BQ-123 ,business.industry ,Vasospasm ,BQ-788 ,Pharmacology ,medicine.disease ,Bosentan ,Endothelins ,Psychiatry and Mental health ,chemistry.chemical_compound ,Cerebral vasospasm ,chemistry ,cardiovascular system ,medicine ,Pharmacology (medical) ,cardiovascular diseases ,Neurology (clinical) ,Endothelin receptor ,Receptor ,business ,circulatory and respiratory physiology ,medicine.drug - Abstract
Summary The actions of the endothelins (endothelin-I. endothelin-2 and endothelin-3) are mediated via endothelin-A (EA) and endothelin-B (ETB) receptors. the former generally mediating vasoconstriction and the latter vasodilation. Peptide antagonists selective for either receptor sUbtype [e.g. BQ 123 (ETA) and BQ 788 (ETB)] and combined ETA/ETB receptor antagonists (e.g. PD 145065 and TAK 044) have been developed. More recently. small molecule non-peptide antagonists have also been synthesised. ETA receptor-selective agents include PD 155080 and BMS 182874. while Ro 46-2005 and bosentan are combined ETA/ETB receptor antagonists. The role of the endothelin family of vasoconstrictor peptides in the pathophysiology of cerebrovascular disease has been speculated upon. Increases in plasma and CSF levels of endothelin-I in delayed vasospasm following subarachnoid haemorrhage and acute ischaemic stroke have implicated the endothelins in these cerebrovascular diseases. The development of non-peptide endothelin receptor antagonists has facilitated investigations into the role of the endothelins in cerebrovascular disease. The endothelin receptor antagonists have been demonstrated to attenuate cerebral vasospasm following experimental subarachnoid haemorrhage in a variety of species. Additionally, the endothelin receptor antagonists ameliorate neuronal damage following eXIkrimental focal and global cerebral ischaemia. These actions have highlighted the therapeutic potential of endothelin receptor antagonists in cerebrovascular disease.
- Published
- 1996
8. The relationship between glutamate release and cerebral blood flow after focal cerebral ischaemia in the cat: effect of pretreatment with enadoline (a kappa receptor agonist)
- Author
-
G.N. Woodruff, Toshal R. Patel, Samuel Galbraith, James McCulloch, and Kenneth B. Mackay
- Subjects
Blood Glucose ,Agonist ,Pyrrolidines ,medicine.drug_class ,Microdialysis ,Excitotoxicity ,Glutamic Acid ,Pharmacology ,medicine.disease_cause ,Body Temperature ,Brain Ischemia ,Stereotaxic Techniques ,Brain ischemia ,chemistry.chemical_compound ,medicine.artery ,medicine ,Animals ,Molecular Biology ,gamma-Aminobutyric Acid ,Benzofurans ,business.industry ,Receptors, Opioid, kappa ,General Neuroscience ,Enadoline ,Penumbra ,Glutamate receptor ,medicine.disease ,chemistry ,Cerebral blood flow ,Cerebrovascular Circulation ,Anesthesia ,Middle cerebral artery ,Cats ,Tyrosine ,Female ,Neurology (clinical) ,business ,Anti-Arrhythmia Agents ,Developmental Biology - Abstract
The effect of the kappa-opioid agonist enadoline (CI-977) upon the relationship between cerebral blood flow and glutamate release was simultaneously assessed (using microdialysis and hydrogen clearance techniques respectively) at the same anatomical locus in the cerebral cortex (suprasylvian gyrus) after permanent middle cerebral artery (MCA) occlusion in halothane-anaesthetised cats. During controlled graded ischaemia, pretreatment with enadoline (0.3 mg/kg i.v. followed by continuous infusion at 0.15 mg/kg/h), initiated 30 min prior to MCA occlusion, significantly attenuated the marked increases in extracellular glutamate, aspartate and GABA observed in the focal ischaemic penumbra. The present data are consistent with the hypothesis that the neuroprotective efficacy of enadoline in focal cerebral ischaemia is due to inhibition of glutamate release in the ischaemic penumbra.
- Published
- 1996
9. AMPA receptor antagonism attenuates MK-801-induced hypermetabolism in the posterior cingulate cortex
- Author
-
Toshal R. Patel and James McCulloch
- Subjects
Male ,Cingulate cortex ,medicine.medical_specialty ,AMPA receptor ,Deoxyglucose ,Gyrus Cinguli ,Rats, Sprague-Dawley ,chemistry.chemical_compound ,Limbic system ,Quinoxalines ,Cortex (anatomy) ,Internal medicine ,Limbic System ,medicine ,Animals ,Tissue Distribution ,Receptors, AMPA ,Molecular Biology ,Behavior, Animal ,General Neuroscience ,Rats ,Dizocilpine ,medicine.anatomical_structure ,Endocrinology ,chemistry ,Posterior cingulate ,Autoradiography ,NMDA receptor ,NBQX ,Neurology (clinical) ,Dizocilpine Maleate ,Stereotyped Behavior ,Developmental Biology ,medicine.drug - Abstract
The effect of pretreatment with an AMPA receptor antagonist, NBQX, on MK-801-induced alterations in glucose use was examined using [14C]-2-deoxyglucose autoradiography. NBQX (7 mg/kg) had minimal effect on glucose utilisation in all anatomical regions examined. The intravenous administration of MK-801 (0.2 mg/kg) induced increases in glucose use in the limbic system and cingulate cortex. MK-801 reduced glucose utilisation in the sensory motor and auditory cortices. Pretreatment with NBQX attenuated the MK-801-induced hypermetabolism in the posterior cingulate cortex. The decreases in glucose utilisation induced by MK-801 were not exacerbated by the pretreatment with NBQX. The interaction between NBQX and MK-801 suggests a possible method of attenuating some of the adverse effects of the non-competitive NMDA receptor antagonists in the posterior cingulate cortex.
- Published
- 1995
10. Postischemic Hypoperfusion in Transient Global Ischemia
- Author
-
James McCulloch and Toshal R. Patel
- Subjects
Pharmacology ,medicine.hormone ,business.industry ,Ischemia ,Blood flow ,medicine.disease ,Bosentan ,Endothelins ,Cerebral blood flow ,Anesthesia ,medicine.artery ,Occlusion ,cardiovascular system ,Medicine ,Common carotid artery ,Cardiology and Cardiovascular Medicine ,business ,Endothelin receptor ,medicine.drug - Abstract
The role of endogenous endothelins (ETs) in mediating postischemic hypoperfusion after transient global ischemia was investigated in halothane-anesthetized rats. Pretreatment with the broad spectrum ET A and ET B antagonist bosentan (17 μmol/kg) had minimal effect on postischemic hypoperfusion, as measured by hydrogen clearance, in the caudate nucleus and the parietal cortex during 3 h after bilateral common carotid artery occlusion with concomitant hemorrhagic hypotension (transient global ischemia). In cerebral blood flow (CBF) measured by [ 14 C]iodoantipyrine autoradiography at 90 min after carotid occlusion with concomitant hemorrhagic hypotension, bosentan treatment failed to alter CBF in any of the cerebral cortical regions examined. No changes in CBF, as measured by hydrogen clearance, were observed after transient bilateral common carotid artery occlusion. [ 14 C]Iodoantipyrine autoradiography at 90 min post occlusion failed to demonstrate any increases in cerebral blood flow after transient bilateral common carotid artery occlusion in any of the 35 brain regions examined in anesthetized rats.
- Published
- 1995
11. Therapeutic Potential of Endothelin Receptor Antagonists in Experimental Stroke
- Author
-
David I. Graham, Annette Marian Doherty, Samuel Galbraith, Moira A. McAuley, James McCulloch, and Toshal R. Patel
- Subjects
Pharmacology ,biology ,business.industry ,Vascular disease ,Fissipedia ,Ischemia ,Laser Doppler velocimetry ,medicine.disease ,biology.organism_classification ,medicine.anatomical_structure ,Cerebral blood flow ,Anesthesia ,cardiovascular system ,medicine ,Cardiology and Cardiovascular Medicine ,business ,Endothelin receptor ,Stroke ,Blood vessel - Abstract
This investigation demonstrates an increase in endothelin (ET)-mediated vascular tone in peri-ischemic areas after experimental focal cerebral ischemia (middle cerebral artery occlusion) in the cat. Adventitial application of the butenolide antagonist PD155080 (30 μM), after MCA occlusions resulted in marked increases in caliber of dilated (10.6 ± 1.6% change from preinjection baseline) and constricted vessels (68.7 ± 17.5% change from preinjection baseline). Cerebral blood flow (measured by laser Doppler flowmetry) was reduced after MCA occlusion to 50% of preocclusion levels. Intravenous administration of PD156707 30 min after MCA occlusion restored cerebral blood flow to preocclusion baseline levels at 6 h. The volume of ischemic damage in the cerebral hemisphere after MCA occlusion was significantly reduced (by 45%) after intravenous administration of PD156707.
- Published
- 1995
12. Effects on feline pial arterioles in situ of bosentan, a non-peptide endothelin receptor antagonist
- Author
-
Moira A. McAuley, James McCulloch, and Toshal R. Patel
- Subjects
Endothelin Receptor Antagonists ,Male ,medicine.hormone ,medicine.medical_specialty ,Muscle, Smooth, Vascular ,Subarachnoid Space ,Injections ,Endothelins ,Cerebral circulation ,Arteriole ,medicine.artery ,Internal medicine ,medicine ,Animals ,Pharmacology ,Sulfonamides ,Vasomotor ,business.industry ,Endothelin receptor antagonist ,Antagonist ,Bosentan ,respiratory tract diseases ,Arterioles ,Endocrinology ,Vasoconstriction ,Cerebrovascular Circulation ,Injections, Intravenous ,Cats ,cardiovascular system ,Female ,Endothelin receptor ,business ,circulatory and respiratory physiology ,medicine.drug - Abstract
The cerebrovascular actions of bosentan, a novel endothelin antagonist with effects at endothelin ETA and ETB receptors, have been examined in individual pial arterioles on the cortical surface of chloralose-anaesthetised cats. Subarachnoid perivascular microapplication of bosentan (0.3-300 microM) had minimal effect on pial arteriolar calibre. Subarachnoid perivascular microapplication of endothelin (10 nM) effected a marked reduction in pial arteriolar calibre (reduced by 39.2 +/- 2.7% from baseline). This vasomotor effect of topical endothelin could be attenuated either by co-administration of bosentan (IC50 approximately 1 microM) or by the intravenous administration of bosentan (17 mumol/kg). These investigations suggest that bosentan (applied topically or systemically) may be a valuable tool in the elucidation of the functional significance of endothelins in the cerebral circulation in vivo.
- Published
- 1994
13. Comparison of cerebral blood flow and injury following intracerebral and subdural hematoma in the rat
- Author
-
Gerald P. Schielke, Toshal R Patel, Julian T. Hoff, A. Lorris Betz, and Richard F. Keep
- Subjects
Male ,medicine.medical_specialty ,Central nervous system ,Ischemia ,Hemodynamics ,Tetrazolium Salts ,Brain Edema ,Brain damage ,Rats, Sprague-Dawley ,Body Water ,Internal medicine ,medicine ,Animals ,Subdural space ,Coloring Agents ,Molecular Biology ,Cerebral Hemorrhage ,Intracerebral hemorrhage ,Ions ,Hematoma ,business.industry ,General Neuroscience ,Cerebral Infarction ,medicine.disease ,Rats ,medicine.anatomical_structure ,Endocrinology ,Hematoma, Subdural ,Cerebral blood flow ,Cerebral cortex ,Anesthesia ,Cerebrovascular Circulation ,Autoradiography ,Neurology (clinical) ,medicine.symptom ,business ,Developmental Biology - Abstract
Subdural hematomas (SDH) can induce ischemia and neuronal damage in the underlying cortex. However, the extent to which intracerebral hematomas (ICH) produce reductions in cerebral blood flow (CBF) sufficient to cause ischemic damage is uncertain. Intracranial hemorrhage was induced by the injection of 100 or 200 microl of blood into the subdural space (SDH) or into the caudate nucleus (ICH) of the rat. CBF was measured using [14C]-iodoantipyrine autoradiography at 4 h. Brain damage was measured using 2,3, 5-triphenyl tetrazolium chloride (TTC) staining at 24 h and brain edema was measured using the wet/dry weight method. Brain ion contents were measured at 24 h using a flame photometer and chloridometer. In the CBF studies, the volume of tissue perfused below the ischemic threshold (
- Published
- 1999
14. Endothelin-mediated vascular tone following focal cerebral ischaemia in the cat
- Author
-
Moira A. McAuley, Toshal R. Patel, Samuel Galbraith, and James McCulloch
- Subjects
medicine.hormone ,medicine.medical_specialty ,Population ,Dioxoles ,030218 nuclear medicine & medical imaging ,Brain Ischemia ,Endothelins ,03 medical and health sciences ,0302 clinical medicine ,Reference Values ,medicine.artery ,Internal medicine ,medicine ,Carnivora ,Animals ,education ,Cerebrospinal Fluid ,education.field_of_study ,Sulfonamides ,biology ,business.industry ,Fissipedia ,Bosentan ,Anatomy ,biology.organism_classification ,Vasomotor System ,Arterioles ,medicine.anatomical_structure ,Neurology ,Vasoconstriction ,Cerebrovascular Circulation ,Middle cerebral artery ,cardiovascular system ,Cardiology ,Cats ,Pia Mater ,Female ,Neurology (clinical) ,Cardiology and Cardiovascular Medicine ,Endothelin receptor ,business ,030217 neurology & neurosurgery ,circulatory and respiratory physiology ,medicine.drug ,Blood vessel - Abstract
The actions of Bosentan and PD155080, nonpeptide endothelin receptor antagonists, were examined in feline pial arterioles in situ following middle cerebral artery (MCA) occlusion to gain insight into the cerebrovascular influence of endogenous endothelins in focal cerebral ischaemia. Immediately following permanent MCA occlusion, all pial arterioles overlying the suprsylvian and ectosylvian gyri displayed marked dilatations, which were maintained in a population of vessel but differentiated into sustained constrictions in others. Perivascular subarachnoid microinjections of Bosentan (30 microM), PD155080 (30 microM), and artificial CSF (pH 7.2) were performed between 30 and 210 min following MCA occlusion. The perivascular microapplication of Bosentan (30 microM) and PD155080 (30 microM) around pial vessels overlying the suprasylvian and ectosylvian gyri, which are within the territory of the occluded MCA, elicited in increase in the calibre of postocclusion dilated and constricted pial arterioles. The perivascular microapplication of PD155080 (30 microM) around postocclusion constricted arterioles overlying the ectosylvian and suprasylvian gyri elicited an increase in the calibre of arterioles (69 +/- 49% from preinjection baseline; n = 8). The perivascular microapplication of Bosentan (30 microM) around postocclusion constricted arterioles overlying the ectosylvian and suprasylvian gyri also elicited an increase in the calibre of arterioles (68 +/- 60% from preinjection baseline; n = 13). In contrast, the microapplication of CSF (pH 7.2) elicited small reductions in pial arteriolar calibre of postocclusion constricted arterioles (-8 +/- 13% from preinjection baseline; n = 8). The perivascular microapplication of PD155080 (30 microM) around postocclusion dilated pial arterioles overlying the ectosylvian and suprasylvian gyri elicited an increase in the calibre of arterioles (11 +/- 10% from preinjection baseline; n = 38). The perivascular microapplication of Bosentan (30 microM) around postocclusion dilated arterioles elicited an increase in the calibre of arterioles (16 +/- 15% from preinjection baseline; n = 36). In contrast, the microapplication of CSF (pH 7.2) elicited small reductions in pial arteriolar calibre of postocclusion dilated arterioles (-9 +/- 6% from preinjection baseline; n = 44). Perivascular microapplication of Bosentan or PD155080 had minimal effect on the calibre of pial arterioles on the parasagittal gyrus (anterior cerebral artery territory), although these arterioles had also displayed sustained dilatation following MCA occlusion. These results indicate that contractile factors (whose effects can be reversed with endothelin receptor antagonists) constrict or impair dilatation of cortical resistance arterioles in an acute cerebral ischaemic episode.
- Published
- 1996
15. Failure of an endothelin antagonist to modify hypoperfusion after transient global ischaemia in the rat
- Author
-
James McCulloch and Toshal R. Patel
- Subjects
medicine.hormone ,Carotid Artery Diseases ,Male ,Time Factors ,Ischemia ,Blood Pressure ,Hemorrhage ,030218 nuclear medicine & medical imaging ,Brain Ischemia ,Endothelins ,Rats, Sprague-Dawley ,03 medical and health sciences ,0302 clinical medicine ,medicine.artery ,Occlusion ,medicine ,Animals ,Common carotid artery ,Carbon Radioisotopes ,Sulfonamides ,business.industry ,Antagonist ,Bosentan ,medicine.disease ,Rats ,Neurology ,Anesthesia ,Cerebrovascular Circulation ,cardiovascular system ,Autoradiography ,Neurology (clinical) ,Hypotension ,Cardiology and Cardiovascular Medicine ,Endothelin receptor ,business ,Perfusion ,030217 neurology & neurosurgery ,Antipyrine ,medicine.drug - Abstract
The role of endogenous endothelins in mediating postischaemic hypoperfusion after transient global ischaemia was investigated in halothane-anaesthetised rats. Pretreatment with the broad-spectrum (ETA and ETB) endothelin antagonist, Bosentan (17μmol/kg) had minimal effect on postischaemic hypoperfusion, measured by hydrogen clearance, in the caudate nucleus and the parietal cortex in the 3 h after bilateral common carotid artery occlusion with concomitant haemorrhagic hypotension (transient global ischaemia). In a separate series of rats with CBF measured by [14C]iodoantipyrine autoradiography at 90 min after carotid occlusion with concomitant haemorrhagic hypotension, Bosentan treatment failed to significantly alter CBF in any of the 35 brain regions examined. No significant alterations in CBF, measured by hydrogen clearance, were observed after transient bilateral common carotid artery occlusion. [14C]Iodoantipyrine autoradiography at 90 min after occlusion failed to demonstrate any significant increases in CBF after transient bilateral common carotid artery occlusion in any of the 35 brain regions examined in anaesthetised rats. The failure of the broad-spectrum endothelin antagonist Bosentan, at concentrations known to inhibit the cerebrovascular effects of exogenous ET-1, provide no support for the view that endothelins have a major role in mediating acute postischaemic hypoperfusion.
- Published
- 1996
16. The Use of Microdialysis for Monitoring the Effect of the Neuroprotective Drug CI-977 on Extracellular Excitatory Amino Acids
- Author
-
Kenneth B. Mackay, Toshal R. Patel, Samuel Galbraith, and James McCulloch
- Subjects
Microdialysis ,business.industry ,Ischemia ,Glutamate receptor ,AMPA receptor ,Brain damage ,Pharmacology ,medicine.disease ,Postsynaptic potential ,medicine ,Excitatory postsynaptic potential ,NMDA receptor ,medicine.symptom ,business - Abstract
The excitatory amino acid glutamate is now accepted as an important cause of brain damage in animals following ischemia [1, 2]. Its effects can be ameliorated by various neuroprotective drugs that either block the postsynaptic N-methyl-d-aspartate (NMDA) and α-amino-3-hydroxy-5-methyl-4-isoxazole propionate (AMPA) receptors or which putatively inhibit the presynaptic release of glutamate [3]. In man, ischemia is a cause of brain damage, not only in stroke but also in head injury; as many as 85% of patients who die following a head injury have evidence of hypoxic ischemic brain damage [4, 5]. The use of neuroprotective drugs in these conditions could be beneficial, and there are currently several clinical studies under way.
- Published
- 1995
Catalog
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.