Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 6 de 6
Filter
Add more filters










Database
Language
Publication year range
3.
Ann R Coll Surg Engl ; 95(1): e7-9, 2013 Jan.
Article in English | MEDLINE | ID: mdl-23317711

ABSTRACT

Pseudocyst formation following acute and chronic pancreatitis is a well known complication. A pancreatic pseudocyst fistulating into the portal vein is a rare and potentially fatal complication. We report a case of pancreatic pseudocyst - portal vein fistula, which was managed with a conservative approach.


Subject(s)
Pancreatic Fistula/etiology , Pancreatic Pseudocyst/etiology , Pancreatitis, Alcoholic/complications , Portal Vein , Vascular Fistula/etiology , Acute Disease , Humans , Male , Middle Aged , Venous Thrombosis/etiology
4.
Neuroscience ; 230: 157-71, 2013 Jan 29.
Article in English | MEDLINE | ID: mdl-23103795

ABSTRACT

Oxidative stress and inflammation play an integral role in the pathogenesis of cerebral ischemia that leads to a cascade of events culminating in the death of neurons and their supporting structures. The signaling pathways that link these events are not fully understood. Recent studies have demonstrated a close link between the nuclear factor-κB (NF-κB) signaling pathway and cerebral ischemia/reperfusion (I/R)-induced inflammation. Flavonoids have been suggested to exert human health benefits by anti-oxidant and anti-inflammatory mechanisms. In this study we undertook a pharmacological approach to investigate the ability of naringenin, a potent flavonoid, to prevent oxidative stress and NF-κB-mediated inflammatory brain damage in the rat model of focal cerebral I/R injury. To test this hypothesis, male Wistar rats were pretreated with naringenin once daily for 21 days and then subjected to 1h of middle cerebral artery occlusion followed by 23 h of reperfusion. Naringenin treatment successfully upregulates the antioxidant status, decreases the infarct size and lowers the levels of myeloperoxidase, nitric oxide and cytokines, besides functional recovery returned close to the baseline. Moreover, immunohistochemical and Western blot analyses clearly demonstrated that naringenin treatment limits glial activation and downregulates the NF-κB expression level and their target genes. These results show, prophylactic treatment with naringenin improved functional outcomes and abrogated the ischemic brain injury by suppressing NF-κB-mediated neuroinflammation. The present study suggests that naringenin may be used as a potential neuroprotectant in patients at high risk of ischemic stroke.


Subject(s)
Flavanones/therapeutic use , Infarction, Middle Cerebral Artery/drug therapy , NF-kappa B/metabolism , Neuroprotective Agents/therapeutic use , Signal Transduction/drug effects , Animals , Brain Infarction/etiology , Brain Infarction/prevention & control , Cytokines/metabolism , Disease Models, Animal , Glial Fibrillary Acidic Protein/metabolism , Glutathione/metabolism , Hand Strength/physiology , Infarction, Middle Cerebral Artery/complications , Lipid Peroxidation/drug effects , Male , Motor Activity/drug effects , Nervous System Diseases/etiology , Nervous System Diseases/prevention & control , Nitric Oxide/metabolism , Peroxidase/metabolism , Peroxisome Proliferator-Activated Receptors/metabolism , Psychomotor Performance/drug effects , Rats , Rats, Wistar , Reperfusion , Thiobarbituric Acid Reactive Substances/metabolism
5.
Br J Radiol ; 80(954): e117-8, 2007 Jun.
Article in English | MEDLINE | ID: mdl-17684071

ABSTRACT

Renal lymphangiectasia is a benign disorder of renal lymphatics. Seldom observed, the pathophysiology is unclear. The clinical course may vary, and management alternatives range from percutaneous drainage in symptomatic cases to pharmacological substitutes in the form of anti-hypertensives and diuretics. We present a case of bilateral perinephric collections on imaging, which presented with gross ascites, abdominal pain and reversible hypertension. Ultrasound examination indicated ascites. Computerized tomography revealed bilateral symmetrical large perinephric collections. This is consistent with the appearance of renal lymphangiectasis (enlarged kidneys with fluid collections seen to be abutting the surrounding structures) reported in the literature. Needle aspiration of the perinephric fluid was undertaken, and laboratory analysis was carried out, which revealed a protein level of 643 mg dl(-1) and a total leucocyte count of 50, of which 80% were lymphocytes. Thereafter, a diagnosis of renal lymphangiectasia was made, and conservative treatment with diuretics and anti-hypertensives was initiated. Reassessment at subsequent follow up visits showed improvement in the patient's clinical condition.


Subject(s)
Kidney Diseases/diagnosis , Lymphangiectasis/diagnosis , Adult , Antihypertensive Agents/therapeutic use , Biopsy, Needle/methods , Diuretics/therapeutic use , Female , Humans , Kidney/diagnostic imaging , Kidney/pathology , Kidney Diseases/diagnostic imaging , Kidney Diseases/drug therapy , Lymphangiectasis/diagnostic imaging , Lymphangiectasis/drug therapy , Tomography, X-Ray Computed/methods
6.
Indian J Med Res ; 94: 241-5, 1991 Jun.
Article in English | MEDLINE | ID: mdl-1937609

ABSTRACT

Hyperthermic effect of arsenic was investigated in rabbits. Injections of arsenic trioxide (0.0001 to 0.1 micrograms) into a lateral cerebral ventricle of the rabbit evoked a dose-dependent hyperthermia, respiratory stimulation and peripheral vasodilatation. Heat loss through respiratory stimulation and peripheral vasodilatation appeared responsible for the long latent period and the slight hypothermia sometimes obtained during this period as these effects followed the same time course. These effects were centrally mediated as demonstrated by the lack of efficacy of the same doses by the intravenous route. The hyperthermic effect of arsenic was antagonized by the sulphydryl donator, dimercaprol, the a-adrenoceptor blocking agent-phenoxybenzamine and the PG-synthesis inhibitor-aspirin. Multiple sites, for antagonistic effects of these substances can be explained by the action of arsenic in inactivating sulphydryl containing enzymes which are many and catalyze diverse biochemical reactions.


Subject(s)
Arsenic/toxicity , Arsenicals , Cerebral Ventricles/drug effects , Fever/chemically induced , Oxides , Animals , Arsenic/antagonists & inhibitors , Arsenic Trioxide , Aspirin/pharmacology , Body Temperature/drug effects , Dimercaprol/pharmacology , Dose-Response Relationship, Drug , Injections, Intraventricular , Male , Phenoxybenzamine/pharmacology , Rabbits
SELECTION OF CITATIONS
SEARCH DETAIL
...