Subject(s)
Colonoscopy/adverse effects , Emphysema/diagnosis , Inflammatory Bowel Diseases/diagnostic imaging , Tomography, X-Ray Computed/adverse effects , Diagnosis, Differential , Emphysema/etiology , Hepatic Veins/diagnostic imaging , Humans , Male , Medical Illustration , Portal Vein/diagnostic imaging , Young AdultABSTRACT
OBJECTIVE: Sinonasal mucosal malignant melanoma is a rare entity. In this report we present a nasal mucosal malignant melanoma case with its histopathological and clinical features. CASE REPORT: An 88-year-old female patient presented with epistaxis a month ago. Examination revealed a polypoid mass lesion of right nasal cavity originating from the middle concha. Her medical history revealed that she had been found to have a mass lesion in the right nasal cavity 15 months ago. She then underwent a punch biopsy from that lesion. A definitive histopathological diagnosis was not made but it was declared that the lesion had been a malignant epithelial tumor. The patient then had radiotherapy and the lesion showed complete regression. One year after completion of radiotherapy, the lesion recurred. Her last PET-CT showed multiple metastatic foci. Endoscopic excisional biopsy was performed for her recurrent lesion. Fragmented tumoral tissues were measured as 3,6x3x0,5 cm. Macroscopically the tumor was brownish in color. Histopathologically the tumor consisted of spindled and epitheloid cells. Immunohistochemically the tumor cells displayed positivity for S-100, HMB-45 and Melan-A. Findings were consistent with malignant melanoma. DISCUSSION: Mucosal malignant melanomas have a poor prognosis despite chemotherapy and radiotherapy. Five-year survival for sinonasal melanoma is reported to be lower than 35%. Sinonasal melanomas show a high recurrence rate. The immunohistochemical markers showing high specificity for malignant melanoma such as S-100, HMB-45 and Melan-A are used in order to reach a correct diagnosis. In our case the tumor showed recurrence and multiple metastases 1 year after completion of radiotherapy. For this recurrent tumor, chemotherapy and radiotherapy have been planned.
Subject(s)
Melanoma/radiotherapy , Nasal Mucosa/pathology , Neoplasm Recurrence, Local/pathology , Paranasal Sinus Neoplasms/radiotherapy , Aged, 80 and over , Biomarkers, Tumor/analysis , Female , Humans , Immunohistochemistry , Melanoma/pathology , Paranasal Sinus Neoplasms/pathologyABSTRACT
BACKGROUND: Epidural anesthesia is known to increase blood flow by producing vasodilatation on mesenteric circulation. In this experimental study, we aim to examine the effect of epidural anesthesia on mesenteric ischemic-reperfusion (IR) injury induced by supracoeliac aortic occlusion in a rabbit model. METHODS: Twenty-eight male white New Zealand rabbits were assigned into 4 separate groups, with 7 rabbits in each group: group I, control group; group II, IR-only group; group III, IR plus epidural anesthesia group; group IV, epidural anesthesia-only group. IR model was produced by clamping supraceliac aorta with an atraumatic vascular clamp for 60 min, followed by reperfusion for 120 min. An epidural catheter was placed via Th12-L1 intervertebral space by using open technique before aortic clamping in those assigned to epidural anesthesia. IR injury was assessed using blood markers interleukin-6 and IMA and tissue markers superoxide dismutase and malondialdehyde. Also histopathological examination was performed to evaluate the degree of injury. RESULTS: All biochemical markers in group II were significantly elevated in comparison with the other 3 groups (p < 0.05). This was paralleled by a more severe histopathological injury in IR- only group (group II). The group receiving IR plus epidural anesthesia (group III) had lower biochemical marker levels as compared with the IR-only group (group II). CONCLUSIONS: Mesenteric IR injury that can occur during abdominal aorta surgery can be reduced by epidural anesthesia, which is commonly used during or after major operations for pain control. Controlled clinical studies are required to evaluate these findings.
Subject(s)
Anesthesia, Epidural , Anesthetics, Local/administration & dosage , Aorta, Abdominal/surgery , Lidocaine/administration & dosage , Mesenteric Arteries/drug effects , Mesenteric Ischemia/prevention & control , Reperfusion Injury/prevention & control , Splanchnic Circulation/drug effects , Vascular Surgical Procedures/adverse effects , Animals , Biomarkers/blood , Constriction , Disease Models, Animal , Interleukin-6/blood , Male , Malondialdehyde/metabolism , Mesenteric Arteries/metabolism , Mesenteric Arteries/pathology , Mesenteric Arteries/physiopathology , Mesenteric Ischemia/blood , Mesenteric Ischemia/pathology , Mesenteric Ischemia/physiopathology , Rabbits , Regional Blood Flow , Reperfusion Injury/blood , Reperfusion Injury/pathology , Reperfusion Injury/physiopathology , Serum Albumin , Serum Albumin, Human , Superoxide Dismutase/metabolism , Time FactorsABSTRACT
We investigated the changes in the serum levels of tumor necrosis factor (TNF)-α and interleukin (IL)-6, the pro-inflammatory cytokines, and the possible effect of melatonin on the modulation of these inflammatory molecules after renal ischemia reperfusion (IR). The study was carried out in the laboratory of Department of Pharmacology. Forty-six male Wistar albino rats were divided into five groups as control (n=6), positive control (n=4), sham (n=12), renal IR (n=12), and renal IR melatonin (n=12). After 1 h renal pedicle occlusion, the blood samples were taken for the measurement of cytokine levels at second hour of the reperfusion. The rats were sacrificed after 24 h of reperfusion for histopathological evaluation. Melatonin or vehicle was administrated to IR rats. Lipopolysaccharide (LPS) was administered to the positive control group and the blood was taken at fourth hour. Serum TNF-α levels increased significantly in renal IR and LPS groups. Serum IL-6 levels were not different from control except the LPS group. There was no significant correlation between the serum TNF-α levels and the histopathological score after renal IR. Melatonin treatment reversed the increase of serum TNF-α levels and histopathological injury in renal tissue after renal IR. Melatonin may have a protective effect by reducing the serum level of TNF-α in renal IR.
Subject(s)
Kidney Diseases , Melatonin/pharmacology , Reperfusion Injury , Animals , Antioxidants/pharmacology , Biological Factors/pharmacology , Inflammation/metabolism , Interleukin-6/metabolism , Kidney/pathology , Kidney Diseases/drug therapy , Kidney Diseases/etiology , Kidney Diseases/metabolism , Lipopolysaccharides/pharmacology , Male , Rats , Rats, Wistar , Reperfusion Injury/drug therapy , Reperfusion Injury/metabolism , Time Factors , Treatment Outcome , Tumor Necrosis Factor-alpha/metabolismABSTRACT
BACKGROUND: Ectopic thyroid tissue very rarely occurs in the buccal region. Even more rarely encountered is the papillary carcinoma arising in the ectopic tissue. METHODS AND RESULTS: We herein present a 78-year-old female patient admitted with a giant, buccal mass that developed within the previous 2 years. Physical examination revealed a vegetative mass on the left buccal region without any cervical lymphadenopathy. Magnetic resonance imaging scan showed an 8- × 6-cm solid mass with cystic components in the left buccal region and thoracic computed tomography scanning revealed pulmonary metastasis. A successful surgery including lower lip splitting was performed, and the mass was totally excised with its surrounding capsule. Histopathologic examination revealed follicular variant of papillary carcinoma of the ectopic thyroid tissue. CONCLUSIONS: To our knowledge, our case is the first case of papillary carcinoma arising from ectopic thyroid tissue in the buccal region in the literature.
Subject(s)
Carcinoma, Papillary/pathology , Choristoma/pathology , Mouth Diseases/complications , Thyroid Gland , Thyroid Neoplasms/pathology , Aged, 80 and over , Biopsy, Needle , Carcinoma, Papillary/etiology , Carcinoma, Papillary/surgery , Cheek/pathology , Choristoma/complications , Female , Humans , Immunohistochemistry , Magnetic Resonance Imaging/methods , Preoperative Care/methods , Rare Diseases , Thyroid Neoplasms/surgery , Tomography, X-Ray Computed/methods , Treatment OutcomeABSTRACT
The therapeutic effects of poly(adenosine diphosphate-ribose) polymerase inhibition by 3-aminobenzamide (3-AB) were investigated in testicular ischemia-reperfusion (I/R) injury, using sperm analysis and histopathological and biochemical examinations, including superoxide dismutase (SOD), catalase (CAT), and glutathione peroxidase (GSH-Px) activities and reduced glutathione (GSH) levels. Male rats were divided into 3 groups: sham (n = 12), I/R (n = 12), and I/R with 3-AB (I/R-3-AB) (n = 12). The left testicular artery was occluded for 1 h, followed by 24 h (for biochemical and histopathological examinations) and 30 days (for sperm analysis) of reperfusion. 3-AB treatment intraperitoneally 10 min prior to and 1 h after reperfusion increased the I/R-induced decrease in sperm motility in both testes and reduced the increased abnormal sperm rates in the ipsilateral testis. However, 3-AB treatment failed to prevent the I/R-induced decrease in sperm concentration in both testes. SOD and CAT activities did not change in any group. GSH-Px activity and GSH levels were increased by I/R. 3-AB treatment reversed the I/R-induced increase in GSH-Px activity, similar to the level in sham rats, but did not alter GSH levels. 3-AB treatment significantly increased the I/R-induced decrease in histopathologic score. In conclusion, 3-AB treatment has potential biochemical and histopathological benefits beyond improving sperm quality and may have the potential to decrease damage from testicular torsion.
Subject(s)
Benzamides/pharmacology , Enzyme Inhibitors/pharmacology , Poly(ADP-ribose) Polymerase Inhibitors , Reperfusion Injury/drug therapy , Reperfusion Injury/prevention & control , Testis/blood supply , Testis/drug effects , Animals , Catalase/metabolism , Glutathione/metabolism , Glutathione Peroxidase/metabolism , Male , Poly(ADP-ribose) Polymerases/metabolism , Rats , Rats, Wistar , Reperfusion , Reperfusion Injury/enzymology , Spermatic Cord Torsion/drug therapy , Spermatozoa/drug effects , Spermatozoa/pathology , Superoxide Dismutase/metabolism , Testicular Diseases/drug therapy , Testicular Diseases/enzymology , Testicular Diseases/prevention & control , Testis/enzymology , Testis/surgeryABSTRACT
Lycopene is one of the major carotenoids and is found almost exclusively in tomatoes and tomato products. This study was performed to evaluate the effect of lycopene on methanol-induced liver injury and to compare the results with those after fomepizole, which is used in treatment of methanol intoxication. Experiments were carried out with 30 female Wistar rats weighting 180-200 g. Rats were injected with a intraperitoneally dose of 3 g/kg methanol as a 50% solution in isotonic saline once for intoxication. Rats were pretreated with fomepizole (50 mg/kg) and/or lycopene (10 mg/kg) before methanol. After 24 hours all the drug-treated and intoxicated rats were sacrificed under anesthesia. Malondialdehyde (MDA) levels were determined in order to assess lipid peroxidation, and caspase-3 activity was determined by immunostaining of liver tissues to evaluate apoptosis. Methanol administration significantly increased the MDA level and caspase-3 activity in liver. Pretreatment with lycopene and/or fomepizole decreased the MDA levels significantly. Similarly, lycopene and fomepizole decreased methanol-induced caspase-3 activity. The findings of the present study demonstrate that methanol intoxication causes hepatic toxicity in rats and that this is likely a result of reactive oxygen species and apoptosis induction. Lycopene has protective effects against methanol-induced hepatic injury similar to fomepizole. It was demonstrated for the first time that both lycopene and fomepizole prevent methanol-induced hepatic injury by reducing the increase of lipid oxidation and caspase-3 activation.
Subject(s)
Carotenoids/therapeutic use , Caspase 3/metabolism , Enzyme Activation/drug effects , Liver Diseases, Alcoholic/drug therapy , Liver/enzymology , Methanol/toxicity , Pyrazoles/therapeutic use , Animals , Disease Models, Animal , Female , Fomepizole , Humans , Liver/drug effects , Liver Diseases, Alcoholic/enzymology , Liver Diseases, Alcoholic/metabolism , Lycopene , Malondialdehyde/metabolism , Methanol/metabolism , Random Allocation , Rats , Rats, WistarABSTRACT
OBJECTIVE: To determine the effect of melatonin, a pineal secretory product that prevents testicular ischemia/reperfusion (IR) injury through its antioxidative properties, on epididymal sperm quality in a rat testicular IR injury model. DESIGN: Experimental study. SETTING: University pharmacology laboratory. ANIMAL(S): Fifty-six 8-week-old male Wistar albino rats. INTERVENTION(S): Left testicular artery and vein occluded for 1 hour; before the bilateral orchiectomy, the organ was allowed to reperfuse 30 days. Melatonin (10 mg/kg IP) or vehicle (1% ethanol in saline) was administrated for 10 minutes before reperfusion and for 1 hour after reperfusion. MAIN OUTCOME MEASURE(S): After 24 hours of reperfusion, the rats were decapitated, and the testicular tissue samples were obtained for histologic examination. In addition, after 30 days of reperfusion, the epididymal sperm concentration, motility, and abnormal sperm rates were determined in the sperm collected from the epididymis. RESULT(S): A statistically significant decrease in sperm concentration resulted from IR as well as an increase in sperm abnormalities, but the sperm motility did not change. Melatonin treatment did not prevent the IR-induced reduction in sperm concentration. However, melatonin treatment statistically significantly decreased the sperm abnormalities when compared with the IR injured samples. CONCLUSION(S): Melatonin may improve sperm morphology for a protective effect in IR-induced testicular injury.
Subject(s)
Epididymis/drug effects , Melatonin/administration & dosage , Reperfusion Injury/prevention & control , Spermatogenesis/drug effects , Spermatozoa/drug effects , Testis/drug effects , Animals , Disease Models, Animal , Epididymis/pathology , Injections, Intraperitoneal , Male , Rats , Rats, Wistar , Reperfusion Injury/pathology , Sperm Count , Sperm Motility/drug effects , Spermatozoa/pathology , Testis/blood supply , Testis/pathology , Time FactorsABSTRACT
Testicular torsion is a common syndrome that could lead to infertility. We investigated the therapeutic effects of lycopene, an antioxidant caretenoid, on testicular ischemia/reperfusion (IR) injury that resembles testicular torsion. Male Wistar albino rats were divided into three groups: sham (n = 6), IR (n = 18), and ischemia/reperfusion with lycopene (IRL, n = 18). Left testicular artery and vein was occluded for 1 h, followed by reperfusion of 3 h, 24 h or 30 days in IR and IRL animals. Either corn oil (vehicle) or lycopene (4 mg/kg) was administrated once daily by gavage to IR or IRL animals, respectively, 5 min after ischemia. Sham-operated animals were treated with vehicle by gavage 5 min after the operation. IR decreased sperm motility and concentration in both ipsilateral and contralateral testes and increased abnormal sperm rate in ipsilateral testis after 30 days of reperfusion. Treatment with lycopene increased the motility in bilateral testes and decreased the rate of abnormal sperm in ipsilateral testis to the sham level, but did not increase sperm concentration in bilateral testes. IR increased the activities of catalase and glutathione peroxidase and the level of reduced glutathione by 24 h of reperfusion, but malondialdehyde remained unchanged. Lycopene treatment restored the enzyme activities but not the reduced glutathione level. Lycopene treatment also ameliorated the IR-induced tissue damage in bilateral testes. In conclusion, the therapeutic antioxidant effect of lycopene on germ cells could serve as a promising intervention to oxidative stress-associated infertility problems, such as testicular torsion.
Subject(s)
Antioxidants/pharmacology , Carotenoids/pharmacology , Reperfusion Injury/complications , Testicular Diseases/etiology , Testicular Diseases/prevention & control , Testis/drug effects , Testis/pathology , Animals , Epididymis/drug effects , Epididymis/metabolism , Lycopene , Male , Rats , Rats, Wistar , Reperfusion Injury/chemically induced , Spermatozoa/metabolismABSTRACT
Desmoplastic infantile gangliogliomas are very rarely encountered, large supratentorial masses, derived from neuroepithelial origin, which have cystic and solid components and contain cells with astrocytic and ganglionic differentiation. These tumors are benign tumors of childhood that become symptomatic when they reach giant sizes. Sixty cases of desmoplastic ganglioglioma have been reported to date. In the present study, a case of giant desmoplastic infantile ganglioglioma in a 22-month-old patient is presented, which had an aggressive radiological appearance in the midline and presented with atypical symptoms.
Subject(s)
Brain Neoplasms/diagnosis , Ganglioglioma/diagnosis , Brain Neoplasms/surgery , Cranial Fossa, Anterior , Craniotomy/methods , Diagnosis, Differential , Ganglioglioma/surgery , Humans , Infant , Magnetic Resonance Imaging , Male , Tomography, X-Ray ComputedABSTRACT
Brown tumors represent the terminal stage of the remodeling process during primary or secondary hyperparathyroidism. We report the first case of brown tumor on the third metatarsal associated with secondary hyperparathyroidism caused by vitamin D deficiency. Radiography showed an expansile tissue mass in the third metatarsal bone. The diagnosis was suggested by the clinical history and was confirmed by biochemical, radiologic, and histopathologic determinations. After intravenous therapy with calcidiol, 1g/d, her symptoms were relieved. The brown tumor showed regression and ossification during the 3 months after therapy.
Subject(s)
Bone Diseases/diagnosis , Bone Diseases/etiology , Hyperparathyroidism, Secondary/complications , Metatarsus , Bone Density Conservation Agents/therapeutic use , Bone Diseases/pathology , Calcifediol/therapeutic use , Calcium/blood , Diagnosis, Differential , Female , Humans , Hyperparathyroidism, Secondary/etiology , Metatarsus/diagnostic imaging , Middle Aged , Radiography , Vitamin D Deficiency/complicationsABSTRACT
OBJECTIVE: To investigate the causes of hypertrophy in recurrent tonsillitis with hypertrophy (RTTH). DESIGN: An immunohistochemical study of recurrent tonsillitis with or without hypertrophy and adenoid tissue. SETTING: Academic medical center. PATIENTS: The study population comprised 15 patients with RTTH, 15 patients with recurrent tonsillitis (RT), 9 patients with adenoid vegetation, and 6 controls. MAIN OUTCOME MEASURES: The following outcome measures were investigated: follicle number and follicular area and circumference; degree of papillary arrangement and keratin cyst in crypts; fibrosis; and density of S-100(+) cells, CD20(+) cells, CD45RO(+) cells, lymphocytes and plasma cells, and cyclin D(1)(+) cells in surface epithelium, crypt epithelium, extrafollicular area, and follicles. RESULTS: In the RTTH group, follicle number and follicular area and circumference, S-100(+) cell density in crypt and surface epithelium, and CD20(+) cell density in crypt epithelium were higher than in the RT group. The other measures were lower in the RTTH group than in the RT group. In patients with RTTH, the increase in follicle number and S-100(+) cell density in surface epithelium and decrease in cyclin D(1)(+) cell density in surface epithelium were significant. The number of CD45RO(+) cells was unchanged, while S-100(+) cell density increased in surface epithelium; however, in the RTTH group, CD20(+) cell density, together with cyclin D(1)(+) cell density, decreased in surface epithelium when compared with the RT group. Also, there was a 50% decrease in cyclin D(1)(+) cell density in follicles, but CD20(+) cell density decreased minimally in follicles. In the RTTH group, the increase or decrease in the number of cyclin D(1)-expressing cells was parallel with the increase or decrease in the number of CD20(+) cells in the areas without follicles. CONCLUSIONS: Tonsil hypertrophy occurred with follicular hyperplasia and hypertrophy. There is a deficiency of proliferating active cells in response to mitogenic stimulation in RTTH. New follicles might have formed with B cells supplied from other sites because of the deficiency of proliferating active cells.
Subject(s)
Lymphocyte Subsets/metabolism , Lymphoid Tissue/immunology , Lymphoid Tissue/pathology , Tonsillitis/immunology , Tonsillitis/pathology , Adolescent , Biomarkers/metabolism , Case-Control Studies , Child , Child, Preschool , Dendritic Cells, Follicular/metabolism , Female , Humans , Hypertrophy , Immunohistochemistry , Lymphocyte Activation , Male , RecurrenceABSTRACT
OBJECTIVE: To determine whether the protective effect of melatonin in testicular ischemia/reperfusion (IR) injury is mediated by the proinflammatory molecules. DESIGN: Experimental study. SETTING: University pharmacology laboratory. ANIMAL(S): Fifty-six 8-week-old male Wistar albino rats. INTERVENTION(S): Left testicular artery and vein was occluded for 1 hour, followed by 3 hours or 24 hours of reperfusion. Melatonin (10 mg/kg IP) or vehicle (1% ethanol in saline) was given 10 minutes before ischemia. MAIN OUTCOME MEASURE(S): Malondialdehyde (MDA), protein carbonyl (PC) content, myeloperoxidase (MPO) activity, and proinflammatory cytokines TNF-alpha, IL-1beta, and IL-6 were examined in testicular tissue after 3 hours of reperfusion. Histologic examination was made after 24 hours of reperfusion. RESULT(S): The MDA, PC, and MPO levels in testicular tissue increased significantly after IR, but the proinflammatory cytokine levels did not change. Melatonin treatment decreased lipid and protein oxidation and ameloriated histopathologic alterations induced by IR without any change in proinflammatory cytokine levels. CONCLUSION(S): The protective effect of melatonin on IR-induced testiculary injury is related to its antioxidant properties but not to proinflammatory cytokines.
Subject(s)
Cytokines/physiology , Inflammation Mediators/physiology , Melatonin/pharmacology , Reperfusion Injury/pathology , Testis/drug effects , Testis/pathology , Animals , Antioxidants/pharmacology , Antioxidants/therapeutic use , Cytoprotection/drug effects , Interleukin-1beta/analysis , Interleukin-6/analysis , Male , Malondialdehyde/analysis , Melatonin/therapeutic use , Peroxidase/analysis , Placebos , Protein Carbonylation , Rats , Rats, Wistar , Reperfusion Injury/prevention & control , Testis/chemistry , Tumor Necrosis Factor-alpha/analysisABSTRACT
Current study was designed to evaluate toxic effects of enrofloxacin on male mice reproductive system. In the treatment group enrofloxacin was administered subcutaneously to male mice at a fixed dose of 150 mg/kg once daily for 15 days, whereas saline solution was given in the same regimen in the control group for the same period. Mice were sacrificed on day 15 and analyzed for sperm quality. In addition to routine examination of sperm material, spermatogenetic activity and organization of each animal were graded according to Johnsen's scoring to assess the spermatogenesis relying on seminiferous tubule cross-section scores. A significant decrease in both epididymal sperm count and sperm motility besides abnormal spermatozoa rate were observed in enrofloxacin group compared to controls (P < 0.01, for all). Johnsen's score in control mice were better than those in treatment group (P < 0.01). These results suggested that a fixed 150 mg/kg dose of enrofloxacin would lead disruption of spermatogenesis in the testes causing deterioration of motility and content of sperms as well as morphological abnormalities.
Subject(s)
Anti-Bacterial Agents/adverse effects , Fluoroquinolones/adverse effects , Spermatozoa/drug effects , Animals , Enrofloxacin , Male , Mice , Sperm Motility/drug effects , Testis/drug effects , Testis/pathologyABSTRACT
We present a case of incisional enteric mucocele formation 10 years following colostomy closure. The patient was admitted to the hospital with the symptoms of an abdominal wall mass lying on previously closed colostomy incision. Clinical presentation, diagnostic work up and pathology of the case were discussed. To our knowledge, this is the first abdominal wall mucocele after colostomy closure reported in the literature.
Subject(s)
Abdominal Wall , Colostomy/adverse effects , Mucocele/etiology , Child , Humans , Male , Mucocele/diagnosis , Mucocele/surgery , Time FactorsABSTRACT
Cavernous malformations are benign vascular lesions of the central nervous system that lack intervening normal brain parenchyma. They can be seen almost anywhere that normal vasculature is available. Lesions are raspberry-like, thin-walled vascular sinusoids without smooth muscles containing hemosiderin deposits. Cerebral cavernous malformations are characterized by small bleedings. Their size varies from a few millimeters to 2- 3 centimeters. Giant cases are rare. Also referred to as cavernoma, these lesions rarely lead to intracerebral hematomas that threaten life. In this report, we have presented a 14-year-old patient with a giant cavernoma leading to a life-threatening massive intracerebral hematoma.
Subject(s)
Cerebral Hemorrhage/diagnostic imaging , Cerebral Hemorrhage/etiology , Hemangioma, Cavernous, Central Nervous System/complications , Hemangioma, Cavernous, Central Nervous System/diagnostic imaging , Tomography, X-Ray Computed , Acute Disease , Adolescent , Cerebral Hemorrhage/pathology , Hemangioma, Cavernous, Central Nervous System/pathology , Humans , MaleABSTRACT
This study was performed to evaluate the effect of melatonin on methanol-induced liver injury. We evaluated the levels of malondialdehyde (MDA), protein carbonylation (PC), myeloperoxidase (MPO) activities and to assess lipid peroxidation, protein oxidation, neutrophil accumulation and nitrite which is a stable end product of nitric oxide respectively. We also studied superoxide dismutase, catalase, and glutathione peroxidase activities of liver tissue to evaluate the changes in the antioxidant status. Histopathological alterations were also determined. The experiment was performed on Wistar rats, which received intragastric 3 g/kg methanol as a 50% solution in isotonic saline once. After 6 and 24 hr all the drug received and intoxicated rats were killed under anesthesia. Pretreatment with melatonin (10 mg/kg) decreased the MDA levels significantly, restored the PC levels to the control, prevented the increase of nitrite level and MPO activity significantly and reversed to the control levels, prevented the reduction in all of the antioxidant enzyme activities. Additionally in melatonin treated group piecemeal necrosis, lobular lytic necrosis, and portal inflammation returned to normal histologic appearances when compared with methanol administration. In conclusion, melatonin has protective effects against methanol-induced hepatic injury.
Subject(s)
Liver/pathology , Melatonin/physiology , Methanol/toxicity , Oxidative Stress/physiology , Animals , Liver/drug effects , Male , Oxidative Stress/drug effects , Rats , Rats, WistarABSTRACT
The pathophysiologic mechanisms leading to acute ischemic renal failure are not completely understood. Melatonin, a compound with well-known antioxidant properties, reduces IR-induced renal injury. The purpose of the present study was to investigate the changes in levels of tumor necrosis factor (TNF)-alpha, IL-beta, and IL-6 in postischemic reperfused renal tissue, and to determine whether the protective effect of melatonin is related the modulation of the production of these inflammatory molecules. Male Wistar albino rats were unilaterally nephrectomized and subjected to 1 hr of renal pedicle occlusion followed by 2 hr or 24 hr of reperfusion. Melatonin (10 mg/kg, i.p.) or vehicle was administrated at 10 min prior to ischemia. After 24 hr of the reperfusion, following decapitation, kidney samples were taken both for histologic examination and for the determination of malondialdehyde (MDA), myeloperoxidase (MPO) activity, total antioxidant capacity (TAC), total oxidative stress (TOS), creatinine, and blood urea nitrogen (BUN). These were measured in serum samples. TNF-alpha, IL-beta, and IL-6 were measured in kidney samples after 2 hr of reperfusion. IR caused a significant increase in renal MDA, MPO, TOS, creatinine, and BUN while decrease TAC without any change in TNF-alpha, IL-beta, and IL-6 levels. Melatonin treatment reduced the biochemical indices without any change in the cytokine levels and ameliorated histopathologic alterations induced by IR. The protective effect of melatonin on IR-induced renal injury is related to its antioxidant properties but not to proinflammatory cytokines.
Subject(s)
Kidney/injuries , Kidney/pathology , Melatonin/pharmacology , Reperfusion Injury/pathology , Reperfusion Injury/prevention & control , Animals , Creatine/blood , Cytokines/metabolism , Kidney/metabolism , Male , Nitrogen/blood , Nitrogen/urine , Oxidative Stress , Phenols/metabolism , Plant Extracts/metabolism , Rats , Rats, Wistar , Reperfusion Injury/metabolismABSTRACT
OBJECTIVE: To investigate widespread disease causes, cellular-structural differences, and steroid response of nasal polyps (NPs). METHOD: Study group consisted of NPs, allergic-NPs, NPs with steroid therapy (ST), antrochoanal polyp (ACP), and controls. We investigated stromal eosinophil, mast cell, CD4+ and CD8+ cell counts and presence of squamous metaplasia, Ki-67 expression, intraepithelial eosinophils-mast cells, epithelial damage, edema, fibrosis, hyalinization, polymorphonuclear leukocyte, and glandular hyperplasia. RESULTS: In allergic-NPs, intraepithelial eosinophils and epithelial damage CD4+ were significantly higher than NPs and also, eosinophils, mast cells, intraepithelial eosinophils, and epithelial damage were significantly higher than ACP. Only stromal eosinophilic infiltration was significantly higher in NPs than ACP. There was significant increased glandular hyperplasia and decreased intraepithelial eosinophils, mast cells, CD4+ cells, squamous metaplasia, and epithelial damage with ST in allergic-NPs. There were no significant differences with ST in NPs. CONCLUSION: NPs in allergic and nonallergic patients may differ in their histology and in their histologic responses to ST. EBM RATING: B-3b.