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1.
J Laryngol Otol ; 134(12): 1060-1064, 2020 Dec.
Article in English | MEDLINE | ID: mdl-33272334

ABSTRACT

OBJECTIVE: To investigate hearing and the take rate of crushed cartilage grafts in tympanoplasty. METHODS: In this double-blinded, randomised, controlled trial, 46 patients with tympanic membrane perforation were enrolled. A conchal cartilage graft was used for reconstruction in both intervention and control groups. In the intervention group, crushed cartilage was used. The success rate and hearing results were ascertained every four months over a one-year follow-up period. RESULTS: A total of 36 patients - 20 in the intervention group and 16 in the control group - completed one year of follow up. There were no statistically significant differences between the two groups in mean air-bone gap, bone conduction threshold, speech discrimination score or speech reception threshold. CONCLUSION: The reduction in living cells after crushed cartilage tympanoplasty may decrease the rigidity and the volume of the graft, but may not necessarily improve the hearing results.


Subject(s)
Bone Conduction/physiology , Cartilage/transplantation , Tympanic Membrane Perforation/surgery , Tympanoplasty/methods , Adult , Audiometry/methods , Audiometry/statistics & numerical data , Double-Blind Method , Fascia/transplantation , Female , Follow-Up Studies , Hearing/physiology , Humans , Male , Middle Aged , Otitis Media/complications , Speech Discrimination Tests/methods , Speech Reception Threshold Test/methods , Treatment Outcome
2.
J Biomed Mater Res A ; 107(9): 2063-2075, 2019 09.
Article in English | MEDLINE | ID: mdl-31081994

ABSTRACT

Treatment of postsurgical infections, associated with orthopedic surgeries, has been a major concern for orthopedics. Several strategies including systematic and local administration of antibiotics have been proposed to this regard. The present work focused on fabricating alginate (Alg) modified brushite (Bru) cements, which could address osteogeneration and local antibiotic demands. To find the proper method of drug incorporation, Gentamicin sulfate (Gen) was loaded into the samples in the form of solution or powder. Several characterization tests including compression test, morphology, cytotoxicity, and cell adhesion assays were carried out to determine the proper concentration of Alg as a modifier of the Bru cement. The results indicated that addition of 1 wt% Alg led to superior mechanical and biological properties of the cement. Moreover, Alg addition changed the morphology of the cement from plate and needle-like structures to petal-like structure. Fourier transform infrared spectroscopy results confirmed the successful loading of Gen on the cements, specifically when Gen solution was used, and X-Ray Diffractometer result indicated that Gen caused a decrease in crystalline size. Furthermore, thermal analysis revealed that Gen-loaded sample had more stable structure as the transformation temperature slightly shifted to a higher one. The stability study confirmed the chemical stability and adequate mechanical performance of the cements within 1 month of soaking time. Finally, the addition of Alg has a positive impact on the release behavior at low concentration of Gen solution so that 20% decrease within 2 weeks of release experiment was remarkably detected.


Subject(s)
Alginates/chemistry , Anti-Bacterial Agents , Bone Cements/chemistry , Calcium Phosphates/chemistry , Gentamicins , Materials Testing , Osteoblasts/metabolism , Anti-Bacterial Agents/chemistry , Anti-Bacterial Agents/pharmacokinetics , Anti-Bacterial Agents/pharmacology , Cell Line , Gentamicins/chemistry , Gentamicins/pharmacokinetics , Gentamicins/pharmacology , Humans , Osteoblasts/cytology
3.
J Mycol Med ; 28(3): 437-442, 2018 Sep.
Article in English | MEDLINE | ID: mdl-29778633

ABSTRACT

Candida species are the commensal organisms of human and animal mucosa that cause a wide range of debilitating diseases in immunocompromised patients and other susceptible individuals. The present study aimed to investigate the ability of clinical isolates of various Candida species to produce proteinase and phospholipase, hydrophobicity and biofilm forming ability that assumed to have a vital role in Candida pathogenicity. Eighty-four Candida strains belonged to Candida albicans (44.1%), C. glabrata (5.9%), C. guilliermondii (5.9%), C. krusei (10.8%), C. parapsilosis (26.2%), and C. tropicalis (7.1%) were examined for proteinase and phospholipase production, cell surface hydrophobicity and biofilm forming ability. The production of proteinase and phospholipase was detected in 81 (96.4%) and 79 (94.1%) of the strains, respectively. C. albicans showed the highest proteinase and phospholipase activity (mean Pz values of 0.42±0.25 and 0.72±0.28) and biofilm formation ability (0.66±0.22). C. parapsilosis had the highest hydrophobicity (42.97±16.1), which showed a good correlation with biofilm formation ability. A considerable percentage of non-albicans Candida strains produced significant amounts of proteinase and phospholipase with a good ability of biofilm formation in vitro. Taken together, our results further substantiated that enzymatic activity, hydrophobicity and the ability for biofilm formation are important virulence factors which may be account for pathogenicity of various Candida species distributed in albicans and non-albicans groups.


Subject(s)
Candida , Candidiasis/microbiology , Peptide Hydrolases/metabolism , Phospholipases/metabolism , Biofilms , Candida/enzymology , Candida/isolation & purification , Candida/pathogenicity , Candida/physiology , Cross Infection/microbiology , Female , Humans , Hydrophobic and Hydrophilic Interactions , Male , Peptide Hydrolases/analysis , Peptide Hydrolases/isolation & purification , Phospholipases/analysis , Phospholipases/isolation & purification , Virulence Factors/physiology
4.
Cell Mol Biol (Noisy-le-grand) ; 62(11): 76-80, 2016 Sep 30.
Article in English | MEDLINE | ID: mdl-27755956

ABSTRACT

The current study is aimed at investigation of the opium effects on the apoptosis of different cell lines in culture medium and compares such effects with one another. The study is carried out on over 8 cell lines (AA8, AGS, Hela, HepG2, MCF7, N2a, PC12, WEHI). A 2.86 x 10-4 g/ml opium concentration was prepared and added to the culture medium of the cell lines for 48 hours. Cytotoxicity was tested by 3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyltetrazolium bromide (MTT) assay. The apoptotic effect of opium on the cell lines was analyzed by Annexin-PI test. Opium with concentration of 2.86 x 10-4 g/ml in 48 hours significantly induces apoptosis in certain cell lines (i.e. AA8, N2a, WEHI), apoptosis and necrosis in some others (i.e. Hela, HepG2, MCF7, and PC12), and also solely necrosis in the AGS cell line. One could infer that the usage of opium with different levels in different tissues leads to certain disorders in some tissues and may have therapeutic effects under distinctive conditions (i.e. unchecked growth of cells) as confirmed by the results.


Subject(s)
Apoptosis/drug effects , Opium/toxicity , Animals , Cell Line , HeLa Cells , Hep G2 Cells , Humans , MCF-7 Cells , PC12 Cells , Rats
5.
Cytokine ; 83: 147-157, 2016 07.
Article in English | MEDLINE | ID: mdl-27152707

ABSTRACT

Recruitment of leukocytes is one of the earliest events in the pathogenesis of ischemic heart disease (IHD) and chemokines play an important role in the migration of these cells into the inflammation sites. The aim of this study was to evaluate the CXCL10, CCL20 and CCL22 levels and the single nucleotide polymorphisms (SNPs) rs4508917, rs6749704 and rs4359426 in chemokine genes in patients with IHD to clarify any association. A total of 300 patients with IHD as having acute myocardial infarction (AMI; n=100), stable angina (SA; n=100) or unstable angina (UA; n=100) and 100 healthy subjects as a control group were enrolled to study. Serum samples from all participants were tested for the CXCL10, CCL20 and CCL22 levels by using ELISA. The SNPs were determined by polymerase chain reaction-restriction length polymorphism (PCR-RFLP) method. The mean serum concentrations of CXCL10, CCL20 and CCL22 in AMI patients (395.97±21.20Pg/mL, 108.38±10.31Pg/mL and 1852.58±205.77Pg/mL), SA patients (405.48±27.36Pg/mL, 90.20±7.69Pg/mL and 2322.04±231.23Pg/mL) and UA patients (396.69±22.79Pg/mL, 141.87±18.10Pg/mL and 2754.89±211.70Pg/mL) were significantly higher than in the healthy group (179.38±8.85Pg/mL, 51.92±4.62Pg/mL and 451.82±23.76Pg/mL, respectively; P<0.001). Similarly, the serum levels of CXCL10, CCL20 and CCL22 in total IHD patients (399.38±13.77Pg/mL, 113.49±7.48Pg/mL and 2309.84±126.39Pg/mL, respectively) were also significantly higher as compared with healthy subjects (P<0.001). The serum levels of CCL20 and CCL22 in UA patients were significantly higher than those in SA and AMI patients, respectively (P<0.01 and P<0.003, respectively). The serum levels of CXCL10 and CCL20 in diabetic patients were significantly higher in comparison to non-diabetic patients (P<0.05 and P<0.02, respectively). The serum levels of CCL22 in dyslipidemic- and obese patients were also significantly higher in comparison with non-dyslipidemic- and non-obese patients, correspondingly (P<0.05 and P<0.01, respectively). There were no significant differences between men and women or between patients who treated with statin, aspirin, ß-blockers or angiotensin converting enzyme (ACE) inhibitors and patients without mentioned treatment regarding the levels of chemokines. The frequency of the GG genotype at SNP rs4508917 in CXCL10 gene was higher, whereas the frequency of the AA genotype at SNP rs4359426 in CCL22 gene was lower in total patients with IHD as compared with healthy subjects (P<0.04 and P<0.002, respectively). These results showed that the higher levels of CXCL10, CCL20 and CCL22 were associated with IHD. The serum levels of chemokines may influence by the certain traditional risk factors of IHD and some studied SNPs, but did not influence by treatment and gender of patients.


Subject(s)
Chemokine CCL20 , Chemokine CCL22 , Chemokine CXCL10 , Myocardial Ischemia/blood , Myocardial Ischemia/genetics , Polymorphism, Single Nucleotide , Adult , Chemokine CCL20/blood , Chemokine CCL20/genetics , Chemokine CCL22/blood , Chemokine CCL22/genetics , Chemokine CXCL10/blood , Chemokine CXCL10/genetics , Female , Humans , Male , Middle Aged , Myocardial Ischemia/therapy
6.
Cell Mol Biol (Noisy-le-grand) ; 62(1): 104-8, 2016 Jan 31.
Article in English | MEDLINE | ID: mdl-26828996

ABSTRACT

Polyomavirus BK is an important risk factor for nephropathy and renal lose after kidney transplantation. CXCL9 is a key immunoregulatory molecule which participates in stimulation and migration of immune cells to the infected sites. Thus, the main aim of this study was to evaluate the expression levels of CXCL9 mRNA and serum levels in the infected polyomavirus BK infected renal transplant patients with and without nephropathy compared with healthy controls. This cross sectional study was performed on three studied groups including: polyomavirus BK infected vs. non-infected renal transplant patients with nephropathy and healthy controls. The mRNA and serum levels of CXCL9 were evaluated on the studied patient and control samples using an in-house comparative real time PCR and ELISA methods, respectively. The mRNA expression and serum levels of CXCL9 were both increased in polyomavirus BK infected compared with non-infected renal transplant patients and also in comparing with healthy controls. This upregulation was significant in the serum level in polyomavirus BK infected vs. non-infected patients and also in comparing with controls. According to these results, polyomavirus BK can induce renal complications via stimulation of inflammatory biomarkers like chemokine. Confirmation of the increasing of the expression and production of CXCL9 as a pro-inflammatory chemokine in renal transplanted polyomavirus BK infected patients with nephropathy need to confirm in further completed studies with longer follow-up.


Subject(s)
BK Virus/pathogenicity , Kidney Diseases/genetics , Kidney Diseases/virology , Polyomavirus Infections/genetics , Biomarkers , Case-Control Studies , Chemokine CXCL9/blood , Cross-Sectional Studies , Humans , Inflammation/blood , Inflammation/genetics , Inflammation/virology , Kidney Transplantation , RNA, Messenger/genetics , Up-Regulation/genetics
7.
Eur Surg Res ; 46(1): 45-51, 2011.
Article in English | MEDLINE | ID: mdl-21150209

ABSTRACT

BACKGROUND/AIMS: The present study examined the preventive effect of ginger against renal ischemia-reperfusion (I-R) injury. METHODS: 30 adult male rats were used. The animals were allocated to five groups of 6 rats: (1) normal (N), (2) normal + ginger (N+G), (3) right nephrectomy (Sham), (4) I-R, and (5) I-R + ginger (I-R+G). To induce renal ischemia, animals were unilaterally nephrectomized and subjected to 45 min of left renal pedicle occlusion with 24 h reperfusion. Ginger was administered orally 24 h and just before ischemia. At the end of the experiment, blood samples and urine were collected. The following renal functional parameters were studied: serum and urinary levels of creatinine and urea, fractional excretion of sodium, and creatinine clearance. Histopathological examination of the kidney was also performed. RESULTS: Rats with renal I-R showed a significant increase in creatinine and urea concentration in serum and also a significant decrease in creatinine clearance compared with the other groups. In addition, renal histopathology in the I-R group showed severe alterations such as tubular dilatation and tubular epithelial necrosis. However, these changes were significantly reduced in the I-R+G group. CONCLUSION: This study suggests that ginger is a useful agent for the prevention of renal ischemia reperfusion-induced injury.


Subject(s)
Phytotherapy , Plant Extracts/therapeutic use , Renal Insufficiency/prevention & control , Reperfusion Injury/prevention & control , Zingiber officinale , Animals , Kidney/pathology , Male , Rats , Rats, Wistar
8.
Int J Dermatol ; 46(7): 711-4, 2007 Jul.
Article in English | MEDLINE | ID: mdl-17614799

ABSTRACT

BACKGROUND: Cutaneous leishmanisis (CL) is a common disease in Iran, particularly in Kerman and Bam and Kerman province. Lymphadenitis resulting from leishmania tropica (dry type) with, or without, cutaneous lesion is rare. Localized leishmanial lymphadenitis (LLA) is a specific clinico-pathologic presentation of inflammatory changes caused by leishmanial parasites or antigen within an isolated lymph node without any systemic manifestation. CASE REPORT: A 55-year-old Iranian woman presented with two slow growing large nodules (masses) on the left preauricular and the left cervical areas. The nodules were large, painless, mobile, multilobulated, and associated with a small skin papule on the left-side of the cheek distal to the masses. RESULTS: Histopathologic examination of both the skin lesion and the lymph nodes suggested the leishmanial etiology of skin papule and lymphadenitis. The Leishman-bodies (amastigotes) were demonstrated in two lymph nodes and a skin lesion. The clinical picture plus pathological finding and the response to meglumine-antimoniate confirmed LLA. CONCLUSION: Lymph node involvement is another rare manifestation of dissemination of infection with dermotropic leishmania. This presentation of CL should not be treated with the ordinary local treatments such as curettage, cryotherapy or surgical excision.


Subject(s)
Leishmania tropica , Leishmaniasis, Cutaneous/pathology , Lymphadenitis/parasitology , Animals , Antiprotozoal Agents/therapeutic use , Female , Humans , Leishmaniasis, Cutaneous/complications , Leishmaniasis, Cutaneous/therapy , Lymphadenitis/drug therapy , Lymphadenitis/pathology , Meglumine/therapeutic use , Meglumine Antimoniate , Middle Aged , Organometallic Compounds/therapeutic use , Skin/pathology
9.
Acta Trop ; 79(2): 129-33, 2001 May 25.
Article in English | MEDLINE | ID: mdl-11369305

ABSTRACT

Lymphadenitis with or without dry-type cutaneous leishmaniasis is rare. The lesion might self heal or show excellent response to antimonial therapy. Routine histopathological changes of localized leishmaniasis lymphadenitis are non-caseating to suppurative granulomata mostly in paracortical areas, some with extension to germinal centres, medullary cords and/or pericapsular spaces which have to be distinguished from other causes of lymphadenitis such as tuberculosis, cat-scratch disease and toxoplasmosis. Dense lymphoplasmocytic infiltrate was observed surrounding the necrotizing granuloma together with dense capsular fibrosis with multiple granulomata in subcapsular and pericapsular areas. Immunostaining of lymph nodes showed that a few macrophages were harbouring Leishman bodies. Dispersed Langerhans cells were also harbouring Leishman bodies in the parasitophorous vacuoles between their cytoplasmic pseudopods. In conclusion multiple noncaseating to suppurative granulomata with dense pericapsular and capsular granulomo-sclerotic changes should be considered in the differential diagnosis of leishmaniasis lymphadenitis.


Subject(s)
Leishmania tropica/isolation & purification , Leishmaniasis, Cutaneous/pathology , Lymphadenitis/pathology , Adolescent , Adult , Animals , Case-Control Studies , Child , Diagnosis, Differential , Female , Humans , Leishmaniasis, Cutaneous/complications , Leishmaniasis, Cutaneous/diagnosis , Lymphadenitis/complications , Lymphadenitis/diagnosis , Male
11.
Acta Trop ; 75(1): 1-7, 2000 Feb 25.
Article in English | MEDLINE | ID: mdl-10708001

ABSTRACT

The skin lesions of five patient volunteers with dry-type cutaneous leishmaniasis were treated by intralesional injection of auto-leukocytes prepared from buffy coat of the patient's own blood. Giemsa stained, air-dried cytological smear preparations were prepared from scrapings taken from the margins of the lesions. The cellular interaction between the organism and the inflammatory response of the host was studied. All lesions showed clinical evidence of regression. The cytological findings suggested progressive degradation of the Leishman donovan (LD) bodies within the parasitophorous vacuoles of the activated macrophages. The parasiticidal effect appeared to be induced by synergistic action of the injected neutrophils and lymphocytes. Due to lack of placebo controls in this study the possibility that, healing might not be related to therapy can not be excluded. This study illustrates the potential for intralesional autotherapy with buffy coat in dry-type cutaneous leishmaniasis.


Subject(s)
Immunotherapy , Leishmaniasis, Cutaneous/therapy , Leukocytes/immunology , Adolescent , Adult , Female , Humans , Injections, Intralesional , Leishmaniasis, Cutaneous/immunology , Leishmaniasis, Cutaneous/parasitology , Leishmaniasis, Cutaneous/pathology , Macrophages/parasitology , Male , Middle Aged , Skin/parasitology , Skin/pathology
13.
14.
Diagn Cytopathol ; 19(3): 182-5, 1998 Sep.
Article in English | MEDLINE | ID: mdl-9740991

ABSTRACT

Exfoliative cytology smears from the lesions of 179 patients with cutaneous leishmaniasis due to Leishmania tropica were studied with specific reference to cellular reactions and their effect on the parasite. Aggregates of the parasite (so-called Leishmania Donovan bodies) were present within macrophages and in some fibroblasts. The nature of the inflammatory reaction to the disease was studied by performing differential counts of the inflammatory cells present in the smears. These were correlated with the number of Leishman Donovan bodies. There was an inverse relationship between the number of Leishman Donovan bodies and the percentage of small lymphocytes, neutrophils, and type I macrophages. It is postulated that aggregates of activated macrophages (designated types II and III) and the Leishmanian milieu (sticky matrix) protect the amastigote Leishmania parasites from being eradicated by the inflammatory and immune reaction. The cytoplasmic blebbing of the parasitophorous vacuoles and cell to cell connection of the activated histiocytes could be shown by the CD-68 immunostaining of the tissue biopsy.


Subject(s)
Leishmania tropica/pathogenicity , Leishmaniasis, Cutaneous/pathology , Adolescent , Adult , Animals , Antigens, CD/metabolism , Antigens, Differentiation, Myelomonocytic/metabolism , Child , Child, Preschool , Cytodiagnosis , Cytoplasm/pathology , Female , Fibroblasts/parasitology , Fibroblasts/pathology , Humans , Immunity, Cellular , Infant , Leishmania tropica/immunology , Leishmania tropica/isolation & purification , Leishmaniasis, Cutaneous/immunology , Leishmaniasis, Cutaneous/metabolism , Leukocyte Count , Macrophages/parasitology , Macrophages/pathology , Male , Middle Aged , Skin/metabolism , Skin/parasitology , Skin/pathology , Ulcer/parasitology , Ulcer/pathology
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