ISSN 2756-3332
Editorial
African Journal of Nursing and Midwifery ISSN 2198-4638 Vol. 7 (7), pp. 001-002, July, 2019. © International Scholars Journals
Editorial
The digitization of medical records
John Ibekwe
Page: 1 - 2
https://doi.org/10.46882/AJNM/1146Review
African Journal of Nursing and Midwifery ISSN 2198-4638 Vol. 7 (7), pp. 001-007, July, 2019. © International Scholars Journals
Review
Regulation of tubulin expression: Multiple overlapping mechanisms
Jennifer Saussede-Aim1* and Charles Dumontet2
1Inserm, U590, Lyon, France.
2Université Lyon 1, ISPB, Lyon, France.
Accepted 09 April, 2019
Abstract
Tubulin is the main constituent of microtubules, a macromolecule participating in a variety of essential cell phenomena. Although the roles of microtubules have been extensively described, the regulation of tubulin expression remains largely unexplored. This review gives an overall view of the regulatory mechanisms of tubulin expression reported in the literature. The first model proposed to explain the regulation of tubulin expression was based on an auto-regulatory mechanism. This hypothesis suggests that soluble tubulin pools regulate the tubulin mRNA levels. This is due to the MREI sequence common to all -tubulin isotypes. Nevertheless this model does not explain variations specific for each tubulin isotype. Transcriptional regulation has been suggested in multiple models. Indeed it appears that certain isotypes are expressed in defined conditions, and that this expression depends on gene regulatory sequences. To illustrate isotype specific regulatory mechanisms, the example of 3-tubulin is presented due to its particular expression pattern as well as its importance in certain physiological phenomena and pharmacological situations.
Key words: Tubulin, expression, regulation.
Charles Dumontet, Jennifer Saussede-Aim*
Page: 1 - 7
https://doi.org/10.46882/AJNM/1145Editorial
African Journal of Nursing and Midwifery ISSN 2198-4638 Vol. 7 (6), pp. 001-002, June, 2019. © International Scholars Journals
Editorial
Health disparity– a concern
John Ibekwe
Page: 1 - 2
https://doi.org/10.46882/AJNM/1144Research Article
African Journal of Nursing and Midwifery ISSN 2198-4638 Vol. 7 (6), pp. 001-007, June, 2019. © International Scholars Journals
Full Length Research Paper
Effects of soy protein on selected enzymes in tissues of rats fed a cholesterol diet
Olarewaju M. Oluba1*, E. Chukwu Onyeneke1, Godwin C. Ojieh2 and George O. Eidangbe2
1Department of Biochemistry, University of Benin, P. M. B. 1154, Benin-City, Nigeria.
2Department of Medical Biochemistry, College of Medicine, Ambrose Alli University, Ekpoma, Nigeria.
Accepted 24 March, 2019
Abstract
Soy protein, an important component of soybeans is unique among plant-based protein because of its associated isoflavones. Isoflavones are a group of compounds with variety of biological properties that may potentially benefit human health. Their actions in various tissues have motivated researchers to access the possible related mechanisms and functions. This study is aimed at determining the effect of soy protein on selected tissue enzymes (used as aids in early diagnosis of cardiovascular disease) in rats fed a cholesterol diet. 24 male Wistar albino rats were assigned randomly into three groups. The first group serving as control was placed on normal diet while groups two and three were fed diet containing 5% cholesterol and 5% cholesterol plus 5% soy protein, respectively. The animals were placed on their respective diet for 7 weeks and at weekly interval LDH, ALT, AST and - GT activities in the liver, kidney and heart were monitored. At the end of the study period, LDH, ALT, AST and -GT activities were substantially reduced in the liver, kidney and heart of rats fed soy protein plus cholesterol diet compared with those fed cholesterol diet without soy protein. These results indicate that soy protein reduces the accumulation of excess fat in the liver, kidney and heart and thus prevent cell death due to lipotoxicity.
Key words: Soy protein, cholesterol, diet, enzyme, lipotoxicity, cardiovascular disease.
Godwin C. Ojieh and George O. Eidangbe, Olarewaju M. Oluba*, E. Chukwu Onyeneke
Page: 1 - 7
https://doi.org/10.46882/AJNM/1143Editorial
African Journal of Nursing and Midwifery ISSN 2198-4638 Vol. 7 (6), pp. 001-002, June, 2019. © International Scholars Journals
Editorial
Research and Development of Drugs – unequal for certain diseases
John Ibekwe
Page: 1 - 2
https://doi.org/10.46882/AJNM/1142Research Article
African Journal of Nursing and Midwifery ISSN 2198-4638 Vol. 7 (5), pp. 001-004, May, 2019. © International Scholars Journals
Full Length Research paper
Evaluation of the association of NOD2/CARD15 gene polymorphisms with clinical course of Turkish Crohn’s disease patients
Fatih Tekin1*, Afig Berdeli2, Omer Ozutemiz1, Ahmet Aydin1, Ahmet Musoglu1, Necla Osmanoglu1 and Tankut Ilter1
1Ege University Medical School, Department of Gastroenterology, Izmir, Turkey.
2Ege University Medical School, Department of Pediatrics, Division of Genetics, Izmir, Turkey.
Accepted 17 March, 2019
Abstract
NOD2/CARD15 gene variants may be associated with distinct phenotypic expressions of Crohn’s disease, however, this association may change according to the ethnic and regional variation. The aim of this study was to analyze the impact of NOD2/CARD15 gene mutations on disease phenotype in Turkish Crohn’s disease patients. Fourty-five Crohn’s disease patients (32 males, 13 females) with a mean age of 38.7 ± 12.1 (range: 19-78) were enrolled into this prospective study. The three major polymorphisms (R702W, G908R, 3020insC) on NOD2/CARD15 gene were studied from the peripheral blood genomic DNA. R702W and G908R mutations were studied by PCR-RFLP method, and 3020insC mutation was studied by DNA sequencing. No homozygous mutation was detected. Heterozygous R702W, G908R, and 3020insC mutations were detected in 4, 3, and 4 patients, respectively. The frequency of R702W, G908R, and 3020insC mutations was found to be 4.4, 3.3, and 4.4%, respectively. The overall mutation frequency was found to be 12.2%. There was no statistically difference between the clinical course of the patients with (n = 11) and without (n = 34) mutations (p>0.05). NOD2/CARD15 gene polymorphisms do not have impact on disease phenotype in Turkish Crohn’s disease patients.
Key words: NOD2/CARD15 gene, Crohn’s disease, phenotype.
Omer Ozutemiz, Fatih Tekin*, Ahmet Musoglu, Necla Osmanoglu and Tankut Ilter, Afig Berdeli, Ahmet Aydin
Page: 1 - 4
https://doi.org/10.46882/AJNM/1141