Assessment of serum total protein, albumin and calcium in pregnant women attending ante-natal clinic, University of Maiduguri Teaching Hospital

Background: Pregnancy is a normal physiological phenomenon with many biochemical changes including calcium metabolism. Calcium requirement increases during pregnancy, thereby increasing the chances of developing hypocalcaemia and hypoalbuminaemia. Aim: The aim of the present study was to assess serum levels of total protein, albumin, and calcium among pregnant women in University of Maiduguri Teaching Hospital Maiduguri, Borno State. Methodology: A total of two hundred (200) subjects were recruited for this study. One hundred and twenty (120) are confirmed pregnant women and 80 non pregnant women age matched were used as controls, out of the 120 pregnant women that participated in the study, 30 were in first trimester, 50 were in second trimester and 40 were in third trimester. Blood chemistry analysis was conducted spectrophotometrically using Biurets method (For Total protein), Bromocresol green method (for Albumin) and O-Cresolphthalein complex one (for calcium). Results: The results show a significant lower value of calcium and albumin (p<0.05) among first trimester pregnant women when compared to the control subjects. The results show a significant decrease in calcium and albumin (p<0.05) among second trimester pregnant women when compared to control subjects. The results show a significant lower value in calcium and albumin (p<0.05) among third trimester pregnant women when compared to control subjects. The results between 1st, 2nd and 3rd trimester pregnant women subjects show a significant difference in calcium and albumin (p<0.05), but there were no significant differences in total protein (p>0.05). The result shows no significant difference in total protein level (p> 0.005)among the first trimester pregnant women when compared to the control subjects. It also shows no any significant difference in total protein level (p> 0.005) among the third trimester pregnant women when compared to the control subjects. Conclusion: There is reduction or decrease in calcium and albumin levels in pregnant women especially in the third trimester. Key words: Pregnancy; Total Protein; Albumin; Calciu

A new horizon of moyamoya disease and associated health risks explored through RNF213

The cerebrovascular disorder moyamoya disease (MMD) was first described in 1957 in Japan, and is typically considered to be an Asian-specific disease. However, it is globally recognized as one of the major causes of childhood stroke. Although several monogenic diseases are known to be complicated by Moyamoya angiopathy, the ring finger protein 213 gene (RNF213) was identified as a susceptibility gene for MMD. RNF213 is unusual, because (1) it induces MMD with no other recognizable phenotypes, (2) the RNF213 p.R4810K variant is an Asian founder mutation common to Japanese, Korean and Chinese with carrier rates of 0.5–2 % of the general population but a low penetrance, and (3) it encodes a relatively largest proteins with a dual AAA+ ATPase and E3 Ligase activities. In this review, we focus on the genetics and genetic epidemiology of RNF213, the pathology of RNF213 R4810K, and the molecular functions of RNF213, and also address the public health contributions to current unresolved issues of MMD. We also emphasize the importance of a more updated definition for MMD, of qualified cohort studies based on genetic epidemiology and an awareness of the ethical issues associated with genetic testing of carriers

Divergent Evolution of CHD3 Proteins Resulted in MOM1 Refining Epigenetic Control in Vascular Plants

Arabidopsis MOM1 is required for the heritable maintenance of transcriptional gene silencing (TGS). Unlike many other silencing factors, depletion of MOM1 evokes transcription at selected loci without major changes in DNA methylation or histone modification. These loci retain unusual, bivalent chromatin properties, intermediate to both euchromatin and heterochromatin. The structure of MOM1 previously suggested an integral nuclear membrane protein with chromatin-remodeling and actin-binding activities. Unexpected results presented here challenge these presumed MOM1 activities and demonstrate that less than 13% of MOM1 sequence is necessary and sufficient for TGS maintenance. This active sequence encompasses a novel Conserved MOM1 Motif 2 (CMM2). The high conservation suggests that CMM2 has been the subject of strong evolutionary pressure. The replacement of Arabidopsis CMM2 by a poplar motif reveals its functional conservation. Interspecies comparison suggests that MOM1 proteins emerged at the origin of vascular plants through neo-functionalization of the ubiquitous eukaryotic CHD3 chromatin remodeling factors. Interestingly, despite the divergent evolution of CHD3 and MOM1, we observed functional cooperation in epigenetic control involving unrelated protein motifs and thus probably diverse mechanisms

Yield and Yield Attributes of Extra-early Maize (Zea Mays L.) as Affected by Rates of Npk Fertilizer Succeeding Chilli Pepper (Capsicum Frutescens) Supplied with Different Rates Sheep Manure

Field experiment was conducted in 2005 and 2006 to study response of extra-early maize variety (95TZEE-Y1) to rates of NPK (0, 40:20:20, 80:40:40 and 120:60:60 kg N:P2O5:K2O ha-1) and residual FYM (0, 5, 10 and 15 t ha-1 applied to chilli pepper the previous season) in the semi-arid zone of Nigeria. Randomized complete block design with three replicates was used. Higher values for soil physical and chemical properties were obtained in plots supplied with manure the previous season with soil from 2006 experiment more fertile than for the first year, hence produced 21% more grain yield. All the applied NPK rates in 2005 and except 40:20:20 ha1 in 2006 had resulted in early maize crop as compared to control. Husked and de-husked cob and 100-grain weights and grain yield/ha were higher at 120:60:60 kg NPK ha-1. Maize grown in plot supplied with 15 t FYM ha1 the previous year matured earlier. Cobs and 100-grain weights and grain yield were highest in plot supplied with 10 t FYM ha1. The 10t FYM ha-1 had 69% and 68% more grain yield than the control in 2005 and 2006, respectively. Highest maize yield was obtained at 120:60:60 kg NPK ha-1 or 10t FYM ha-1. All the parameters measured significantly and positively related to each other when the two years data were combined

Structural and functional analyses of the DMC1-M200V polymorphism found in the human population

The M200V polymorphism of the human DMC1 protein, which is an essential, meiosis-specific DNA recombinase, was found in an infertile patient, raising the question of whether this homozygous human DMC1-M200V polymorphism may cause infertility by affecting the function of the human DMC1 protein. In the present study, we determined the crystal structure of the human DMC1-M200V variant in the octameric-ring form. Biochemical analyses revealed that the human DMC1-M200V variant had reduced stability, and was moderately defective in catalyzing in vitro recombination reactions. The corresponding M194V mutation introduced in the Schizosaccharomyces pombe dmc1 gene caused a significant decrease in the meiotic homologous recombination frequency. Together, these structural, biochemical and genetic results provide extensive evidence that the human DMC1-M200V mutation impairs its function, supporting the previous interpretation that this single-nucleotide polymorphism is a source of human infertility

Bone marrow stromal cells attenuate sepsis via prostaglandin E2— dependent reprogramming of host macrophages to increase their interleukin-10 production

Sepsis causes over 200,000 deaths yearly in the US; better treatments are urgently needed. Administering bone marrow stromal cells (BMSCs—also known as mesenchymal stem cells) to mice before or shortly after inducing sepsis by cecal ligation and puncture reduced mortality and improved organ function. The beneficial effect of BMSCs was eliminated by macrophage depletion or pretreatment with antibodies specific for interleukin-10 (IL-10) or IL-10 receptor. Monocytes and/ or macrophages from septic lungs made more IL-10 when prepared from mice treated with BMSCs versus untreated mice. Lipopolysaccharide (LPS)-stimulated macrophages produced more IL-10 when cultured with BMSCs, but this effect was eliminated if the BMSCs lacked the genes encoding Toll-like receptor 4, myeloid differentiation primary response gene-88, tumor necrosis factor (TNF) receptor-1a or cyclooxygenase-2. Our results suggest that BMSCs (activated by LPS or TNF-α) reprogram macrophages by releasing prostaglandin E2 that acts on the macrophages through the prostaglandin EP2 and EP4 receptors. Because BMSCs have been successfully given to humans and can easily be cultured and might be used without human leukocyte antigen matching, we suggest that cultured, banked human BMSCs may be effective in treating sepsis in high-risk patient groups.Sepsis, a serious medical condition that affects 18 million people per year worldwide, is characterized by a generalized inflammatory state caused by infection. Widespread activation of inflammation and coagulation pathways progresses to multiple organ dysfunction, collapse of the circulatory system (septic shock) and death. Because as many people die of sepsis annually as from acute myocardial infarction1, a new treatment regimen is desperately needed. In the last few years, it has been discovered that BMSCs are potent modulators of immune responses2-5. We wondered whether such cells could bring the immune response back into balance, thus attenuating the underlying pathophysiology that eventually leads to severe sepsis, septic shock and death6,7. As a model of sepsis, we chose cecal ligation and puncture (CLP), a procedure that has been used for more than two decades8. This mouse model closely resembles the human disease: it has a focal origin (cecum), is caused by multiple intestinal organisms, and results in septicemia with release of bacterial toxins into the circulation. With no treatment, the majority of the mice die 24-48 h postoperatively. Originally published Nature Medicine, Vol. 15, No. 1, Jan 200

Activation of Cytotoxic and Regulatory Functions of NK Cells by Sindbis Viral Vectors

Oncolytic viruses (OVs) represent a relatively novel anti-cancer modality. Like other new cancer treatments, effective OV therapy will likely require combination with conventional treatments. In order to design combinatorial treatments that work well together, a greater scrutiny of the mechanisms behind the individual treatments is needed. Sindbis virus (SV) based vectors have previously been shown to target and kill tumors in xenograft, syngeneic, and spontaneous mouse models. However, the effect of SV treatment on the immune system has not yet been studied. Here we used a variety of methods, including FACS analysis, cytotoxicity assays, cell depletion, imaging of tumor growth, cytokine blockade, and survival experiments, to study how SV therapy affects Natural Killer (NK) cell function in SCID mice bearing human ovarian carcinoma tumors. Surprisingly, we found that SV anti-cancer efficacy is largely NK cell-dependent. Furthermore, the enhanced therapeutic effect previously observed from Sin/IL12 vectors, which carry the gene for interleukin 12, is also NK cell dependent, but works through a separate IFNγ-dependent mechanism, which also induces the activation of peritoneal macrophages. These results demonstrate the multimodular nature of SV therapy, and open up new possibilities for potential synergistic or additive combinatorial therapies with other treatments