6 research outputs found

    Therapeutic Potential of Bone Marrow Derived Mesenchymal Stem Cells in Modulating Astroglyosis of Surgical Induced Experimental Spinal Cord Injury

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    Background: Spinal cord injury (SCI) unsuccessful regeneration was due to glial scar development. It was a major obstacle to axonal restoration. Safe therapeutic intervention by the use of bone marrow derived stem cells (BMMSCs) transplantation applied in the present study could reduce spinal disability. Material and methods: Forty male albino rats were divided into four groups: GI: negative control (n = 10 rats); GII: positive control after SCI (n = 10 rats); GIII: SCI + BM − MSCs intravenous injected and GIV: SCI + BM − MSCs intra lesion injected (n = 10 rats in each group). The samples were taken from spinal cord tissues around the region of injury and were subjected to histological, immunohistochemical assessment. RNA extraction and real time PCR for detection of nerve regeneration and astrocyte response to the injury were also performed. Results: Clinical improvement occurred by the enhancement in the Basso, Beattie and Bresnahan (BBB) score after SCI. Histological examinations showed positive regenerative responses in GIV compared to GIII. Conclusion: BM-MSCs transplantation has a promising role in enhancing the microenvironment for nerve regeneration through stumbling the glial scaring formation and inflammatory response af- ter chronic spinal cord injury especially by using intra-lesion route injection

    Assessment of neutrophil/lymphocyte percentage in bronchial asthma

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    Background Neutrophil/lymphocyte percentage is a helpful test for evaluation of systemic inflammation. This study aimed to investigate neutrophil/lymphocyte percentage as an evidence of control status in bronchial asthma. Patients and methods The study included 45 (20 males and 25 females) patients and 45 apparently healthy subjects. Full clinical evaluation, complete blood count (CBC) with differential white blood cell count, Erythrocyte sedimentation rate (ESR), C-reactive protein (CRP), and total IgE measurement were done for participants. Results Neutrophil/lymphocyte percentage and CRP were higher in asthmatics than controls (statistically significant difference), and they were significantly increased with uncontrolled asthma. Neutrophil/lymphocyte percentage could predict uncontrolled asthma with a sensitivity of 66.7%, specificity of 75.6%, positive predictive value of 73.2%, negative predictive value of 69.4% and accuracy of 71.1%. Neutrophil/lymphocyte percentage increased in asthmatics with asthma control test (ACT) less than 20 versus patients with ACT of at least 20 (statistically significant difference), whereas neutrophil/lymphocyte percentage did not differ significantly among the patients with asthma regarding sex and smoking. Neutrophil/lymphocyte percentage had direct proportional relation with CRP and ACT, whereas the relations between neutrophil/lymphocyte percentage and age, eosinophils, IgE, Forced expiratory volume in first second (FEV1%), duration of the disease, or number of attacks per year were nonsignificant. No significant correlation was found between controlled and uncontrolled cases regarding total leukocyte count (TLC), duration, and onset of the disease. The number of attacks was significantly higher in uncontrolled cases than controlled ones. Conclusion Neutrophil/lymphocyte percentage could predict uncontrolled asthma with high sensitivity and specificity. Neutrophil/lymphocyte percentage is a rapid, inexpensive method with routine CBC analysis and could be a useful predictor of asthma control

    Does vitamin C have the ability to augment the therapeutic effect of bone marrow-derived mesenchymal stem cells on spinal cord injury?

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    Methylprednisolone (MP) is currently the only drug confirmed to exhibit a neuroprotective effect on acute spinal cord injury (SCI). Vitamin C (VC) is a natural water-soluble antioxidant that exerts neuroprotective effects through eliminating free radical damage to nerve cells. Bone marrow mesenchymal stem cells (BMMSCs), as multipotent stem cells, are promising candidates in SCI repair. To evaluate the therapeutic effects of MP, VC and BMMSCs on traumatic SCI, 80 adult male rats were randomly divided into seven groups: control, SCI (SCI induction by weight-drop method), MP (SCI induction, followed by administration of 30 mg/kg MP via the tail vein, once every other 6 hours, for five times), VC (SCI induction, followed by intraperitoneal administration of 100 mg/kg VC once a day, for 28 days), MP + VC (SCI induction, followed by administration of MP and VC as the former), BMMSCs (SCI induction, followed by injection of 3 × 106 BMMSCs at the injury site), and BMMSCs + VC (SCI induction, followed by BMMSCs injection and VC administration as the former). Locomotor recovery was assessed using the Basso Mouse Scale. Injured spinal cord tissue was evaluated using hematoxylin-eosin staining and immunohistochemical staining. Expression of transforming growth factor-beta, tumor necrosis factor-alpha, and matrix metalloproteinase-2 genes was determined using real-time quantitative PCR. BMMSCs intervention better promoted recovery of nerve function of rats with SCI, mitigated nerve cell damage, and decreased expression of transforming growth factor-beta, tumor necrosis factor-alpha, and matrix metalloproteinase-2 genes than MP and/or VC. More importantly, BMMSCs in combination with VC induced more obvious improvements. These results suggest that VC can enhance the neuroprotective effects of BMMSCs against SCI

    Clinical and genetic characterization of ten Egyptian patients with Wolf–Hirschhorn syndrome and review of literature

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    Abstract Background Wolf–Hirschhorn syndrome (WHS) (OMIM 194190) is a multiple congenital anomalies/intellectual disability syndrome. It is caused by partial loss of genetic material from the distal portion of the short arm of chromosome. Methods We studied the phenotype–genotype correlation. Results We present the clinical manifestations and cytogenetic results of 10 unrelated Egyptian patients with 4p deletions. Karyotyping, FISH and MLPA was performed for screening for microdeletion syndromes. Array CGH was done for two patients. All patients exhibited the cardinal clinical manifestation of WHS. FISH proved deletion of the specific WHS locus in all patients. MLPA detected microdeletion of the specific locus in two patients with normal karyotypes, while array CGH, performed for two patients, has delineated the extent of the deleted segments and the involved genes. LETM1, the main candidate gene for the seizure phenotype, was found deleted in the two patients tested by array CGH; nevertheless, one of them did not manifest seizures. The study emphasized the previous. Conclusion WHS is a contiguous gene syndrome resulting from hemizygosity of the terminal 2 Mb of 4p16.3 region. The Branchial fistula, detected in one of our patients is a new finding that, to our knowledge, was not reported
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