African Journal of Nursing and Midwifery

ISSN 2756-3332

Table of Contents 2019

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/1146

Review

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/1145

Editorial

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/1144

Research 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/1143

Editorial

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/1142

Research 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