The Determinants of Student Performance in Indonesian Public Primary Schools: the Role of Teachers and Schools

In this paper we investigate the determinants of student performance in mathematics and dictation tests among fourth-grade school children in Indonesia. we use a unique dataset of school and student information that was collected in a nationally representative survey of 110 public schools in 8 Indonesian provinces in 2003. using an ols regression technique that compensates for heteroskedasticity, we conduct separate sets of student-level regressions for three performance variables: math scores, dictation scores and combined scores. we found that student performance is strongly influenced by individual variables, teacher variables and school variables. among the significant variables are the education level of parents; student-teacher ratio; quality of school facilities and teacher absence rate. we also discuss the policy implications of the results. key words: absenteeism; primary school; achievement

Plasmalogen Deficiency: A Risk Factor for Dementias and Potential Treatment Target

Altered lipid metabolism is implicated in the risk of sporadic Alzheimer’s disease (AD) and related dementias (ADRD); however, the precise mechanisms accounting for findings from observational studies remains to be fully elucidated. Plasmalogens are a subclass of integral membrane phospholipids with unique properties that appear to play important roles relevant to the pathophysiology of AD and ADRD, including vesicle fusion necessary for synaptic neurotransmitter release, modulation of membrane fluidity and microdomain dynamics, membrane antioxidant functions, and neuroprotection. Like the more familiar phosphatides, plasmalogens are synthesized on a 3-carbon glycerol backbone; however, they differ from phosphatides by the presence of a vinyl ether linkage at the 1st (sn1) glycerol carbon atom in place of the acyl ester linkage present at sn1 in phosphatides, and at sn2 in both lipid subclasses. Plasmalogens bearing the omega-3 fatty acid docosahexaenoic acid (DHA), a key component of fish oils, are the most abundant plasmalogen species in cerebral cortex membranes. Circulating plasmalogen levels are decreased in older individuals, and are further decreased in AD and Mild Cognitive Impairment (MCI). In addition, reduced indices of plasmalogen biosynthesis and/or remodeling are significantly correlated with elevated cerebrospinal fluid (CSF) concentrations of total tau, which is a biomarker of AD and certain other neurodegenerative diseases. This correlation suggests a functional relationship between reduced plasmalogen availability and neurodegeneration. Endogenous plasmalogen synthesis requires the integrity of peroxisomes for the attachment of an alkyl side chain to the sn1 glycerol carbon. Decreased peroxisome function may be a key factor underlying the decrease in circulating plasmalogens with aging and with neurodegenerative diseases such as AD and ADRD. Preclinical data indicate that oral administration of a precursor phospholipid compound, DHA-containing alkyl-diacylglycerol, or DHA-AAG, can increase circulating DHA-containing plasmalogens in a peroxisome-independent manner, as conversion to plasmalogens from this precursor requires only the endoplasmic reticulum. We present here data showing that: 1) oral administration of a single dose of DHA-AAG at 100mg/kg to 6 (4M/2F) healthy subjects aged 23-56 increased circulating plasmalogen levels by 80% within 24 hours; and 2) daily oral administration of DHA-AAG to 22 persons (11M/11F), aged 37-84 (mean= 69) yr, with mild to moderate cognitive impairment [CDR: 0.5 (N=14); 1 (N=4); 2 (N = 4)] on an ascending-dose schedule of 1.0 ml/day for 30 days, followed by 2.0 ml/day for 60 days, followed by 4.0 ml for 30 days, increased serum DHA plasmalogens by \u3e 2-fold by the end of the treatment period. DHA-AAG was well-tolerated by both groups of individuals in these 2 studies. These findings suggest that DHA-AAG may be a useful agent for correcting plasmalogen deficiency associated with aging and aging-associated cognitive disorders. Future studies will examine the effect of plasmalogen repletion with DHA-AAG on cerebrospinal fluid plasmalogen concentrations, and effects on cognitive function and other clinical outcomes

Pelatihan Penulisan Karya Ilmiah (Penelitian Tindakan Kelas sebagai Inspirasi Guru Profesional)

Pelatihan Penulisan Karya ilmiah ini merupakan bentuk pengabdian pada masyarakat. Kegiatan pelatihan ini fokus pada Penelitian Tindakan Kelas. Pelatihan ini bertujuan (1) memberikan pemahaman kepada guru terhadap pentingnya Penelitian Tindakan Kelas (2) para guru mampu mengaplikasikan konsep dan pemahaman Penelitian Tindakan Kelas pada pelaksanaan dan evaluasi proses pembelajaran. Lokasi kegiatan ini di Kecamatan Kopang, Kabupaten Lombok Tengah. Peserta pelatihan adalah para guru di tingkat Sekolah Dasar dan Menengah Pertama se-Kecamatan Kopang Kabupaten Lombok Tengah. Peserta yang hadir pada pelatihan ini sebanyak 35 peserta. Metode yang digunakan dalam pelatihan ini adalah ceramah bervariasi dalam bentuk seminar sehari. Peserta terlihat aktif dan semangat mengikuti pelatihan. Hal ini ditandai dengan pertanyaan yang diajukan oleh para peserta. Berdasarkan temuan hasil diskusi bahwa pelatihan penelitian tindakan kelas memberikan inspirasi tersendiri bagi guru. Kegiatan semacam ini yang jarang dilaksanakan didaerah. Peserta akan mengaplikasikan penelitian tindakan kelas dengan harapan ada proses pendampingan yang berkelanjutan

Pharmacometabolomics reveals racial differences in response to atenolol treatment.

Antihypertensive drugs are among the most commonly prescribed drugs for chronic disease worldwide. The response to antihypertensive drugs varies substantially between individuals and important factors such as race that contribute to this heterogeneity are poorly understood. In this study we use metabolomics, a global biochemical approach to investigate biochemical changes induced by the beta-adrenergic receptor blocker atenolol in Caucasians and African Americans. Plasma from individuals treated with atenolol was collected at baseline (untreated) and after a 9 week treatment period and analyzed using a GC-TOF metabolomics platform. The metabolomic signature of atenolol exposure included saturated (palmitic), monounsaturated (oleic, palmitoleic) and polyunsaturated (arachidonic, linoleic) free fatty acids, which decreased in Caucasians after treatment but were not different in African Americans (p<0.0005, q<0.03). Similarly, the ketone body 3-hydroxybutyrate was significantly decreased in Caucasians by 33% (p<0.0001, q<0.0001) but was unchanged in African Americans. The contribution of genetic variation in genes that encode lipases to the racial differences in atenolol-induced changes in fatty acids was examined. SNP rs9652472 in LIPC was found to be associated with the change in oleic acid in Caucasians (p<0.0005) but not African Americans, whereas the PLA2G4C SNP rs7250148 associated with oleic acid change in African Americans (p<0.0001) but not Caucasians. Together, these data indicate that atenolol-induced changes in the metabolome are dependent on race and genotype. This study represents a first step of a pharmacometabolomic approach to phenotype patients with hypertension and gain mechanistic insights into racial variability in changes that occur with atenolol treatment, which may influence response to the drug

Dietary Isomalto/Malto-Polysaccharides Increase Fecal Bulk and Microbial Fermentation in Mice

Scope: The prevalence of metabolic-syndrome-related disease has strongly increased. Nutritional intervention strategies appear attractive, particularly with novel prebiotics. Isomalto/malto-polysaccharides (IMMPs) represent promising novel prebiotics that promote proliferation of beneficial bacteria in vitro. The present study investigates for the first time the in vivo effects of IMMP in mice. Methods and results: C57BL/6 wild-type mice received control or IMMP-containing (10%, w/w) diets for 3 weeks. IMMP leads to significantly more fecal bulk (+26%, p < 0.05), higher plasma non-esterified fatty acids (colorimetric assay, +10%, p < 0.05), and lower fecal dihydrocholesterol excretion (mass spectrometry, −50%, p < 0.05). Plasma and hepatic lipid levels (colorimetric assays following lipid extraction) are not influenced by dietary IMMP, as are other parameters of sterol metabolism, including bile acids (gas chromatography/mass spectrometry). IMMP is mainly fermented in the cecum and large intestine (high-performance anion exchange chromatography). Next-generation sequencing demonstrates higher relative abundance of Bacteroides and butyrate producers (Lachnospiraceae, Roseburia Odoribacter) in the IMMP group. Conclusion: The combined results demonstrate that IMMP administration to mice increases fecal bulk and induces potentially beneficial changes in the intestinal microbiota. Further studies are required in disease models to substantiate potential health benefits.</p

A chinrest-based approach to measure eye movements and experimental task engagement in macaques with minimal restraint

\ua9 2024 The AuthorsBackground: The use of Rhesus macaques in vision research is crucial due to their visual system\u27s similarity to humans. While invasive techniques have been the norm, there has been a shift towards non-invasive methods, such as facemasks and head molds, to enhance animal welfare and address ethical concerns. New Method: We present a non-invasive, 3D-printed chinrest with infrared sensors, adapted from canine research, allowing for accurate eye movement measurements and voluntary animal participation in experiments. Results: The chinrest method showed a 16% and 28% increase in average trial numbers for Monkey 1 and Monkey 2, respectively, compared to the traditional headpost method. The engagement was high, with monkeys performing over 500 trials per session and initiating a new trial after an average intertrial interval of approximately 1 second. The hit rate improved by about 10% for Monkey 1 in the chinrest condition, and the fixation precision, measured by the standard deviation of gaze positions, was significantly better in the chinrest condition, with Monkey 1 showing a reduction in fixation imprecision from 0.26\ub0 to 0.17\ub0 in the X-axis. Comparison with Existing Methods: The chinrest approach showed significant improvements in trial engagement and reduction in aborted trials due to fixation breaks, indicating less stress and potentially improved data quality compared to previous non-invasive methods. Conclusions: The chinrest method offers a significant advancement in primate cognitive testing by allowing for precise data collection while addressing animal welfare concerns, possibly leading to better scientific outcomes and a paradigm shift in primate research methodologies

Long-Term beta-galacto-oligosaccharides Supplementation Decreases the Development of Obesity and Insulin Resistance in Mice Fed a Western-Type Diet

Scope: The gut microbiota might critically modify metabolic disease development. Dietary fibers such as galacto-oligosaccharides (GOS) presumably stimulate bacteria beneficial for metabolic health. This study assesses the impact of GOS on obesity, glucose, and lipid metabolism. Methods and results: Following Western-type diet feeding (C57BL/6 mice) with or without β-GOS (7% w/w, 15 weeks), body composition, glucose and insulin tolerance, lipid profiles, fat kinetics and microbiota composition are analyzed. GOS reduces body weight gain (p < 0.01), accumulation of epididymal (p < 0.05), perirenal (p < 0.01) fat, and insulin resistance (p < 0.01). GOS-fed mice have lower plasma cholesterol (p < 0.05), mainly within low-density lipoproteins, lower intestinal fat absorption (p < 0.01), more fecal neutral sterol excretion (p < 0.05) and higher intestinal GLP-1 expression (p < 0.01). Fecal bile acid excretion is lower (p < 0.01) in GOS-fed mice with significant compositional differences, namely decreased cholic, α-muricholic, and deoxycholic acid excretion, whereas hyodeoxycholic acid increased. Substantial changes in microbiota composition, conceivably beneficial for metabolic health, occurred upon GOS feeding. Conclusion: GOS supplementation to a Western-type diet improves body weight gain, dyslipidemia, and insulin sensitivity, supporting a therapeutic potential of GOS for individuals at risk of developing metabolic syndrome

The Giardia lamblia vsp gene repertoire: characteristics, genomic organization, and evolution

BACKGROUND:Giardia lamblia trophozoites colonize the intestines of susceptible mammals and cause diarrhea, which can be prolonged despite an intestinal immune response. The variable expression of the variant-specific surface protein (VSP) genes may contribute to this prolonged infection. Only one is expressed at a time, and switching expression from one gene to another occurs by an epigenetic mechanism.RESULTS:The WB Giardia isolate has been sequenced at 10x coverage and assembled into 306 contigs as large as 870 kb in size. We have used this assembly to evaluate the genomic organization and evolution of the vsp repertoire. We have identified 228 complete and 75 partial vsp gene sequences for an estimated repertoire of 270 to 303, making up about 4% of the genome. The vsp gene diversity includes 30 genes containing tandem repeats, and 14 vsp pairs of identical genes present in either head to head or tail to tail configurations (designated as inverted pairs), where the two genes are separated by 2 to 4 kb of non-coding DNA. Interestingly, over half the total vsp repertoire is present in the form of linear gene arrays that can contain up to 10 vsp gene members. Lastly, evidence for recombination within and across minor clades of vsp genes is provided.CONCLUSIONS:The data we present here is the first comprehensive analysis of the vsp gene family from the Genotype A1 WB isolate with an emphasis on vsp characterization, function, evolution and contributions to pathogenesis of this important pathogen.This item is part of the UA Faculty Publications collection. For more information this item or other items in the UA Campus Repository, contact the University of Arizona Libraries at [email protected]

The Kynurenine Pathway Is Upregulated by Methyl-deficient Diet and Changes Are Averted by Probiotics

Scope Probiotics exert immunomodulatory effects and may influence tryptophan metabolism in the host. Deficiency of nutrients related to C1 metabolism might stimulate inflammation by enhancing the kynurenine pathway. This study used Sprague Dawley rats to investigate whether a methyl-deficient diet (MDD) may influence tryptophan/kynurenine pathways and cytokines and whether probiotics can mitigate these effects. Methods and Results Rats are fed a control or MDD diet. Animals on the MDD diet received vehicle, probiotics (L. helveticus R0052 and B. longum R0175), choline, or probiotics + choline for 10 weeks (n = 10 per group). Concentrations of plasma kynurenine metabolites and the methylation and inflammatory markers in plasma and liver are measured. Results MDD animals (vs controls) show upregulation of plasma kynurenine, kynurenic acid, xanthurenic acid, 3-hydroxyxanthranilic acid, quinolinic acid, nicotinic acid, and nicotinamide (all p < 0.05). In the MDD rats, the probiotics (vs vehicle) cause lower anthranilic acid and a trend towards lower kynurenic acid and picolinic acid. Compared to probiotics alone, probiotics + choline is associated with a reduced enrichment of the bacterial strains in cecum. The interventions have no effect on inflammatory markers. Conclusions Probiotics counterbalance the effect of MDD diet and downregulate downstream metabolites of the kynurenine pathway.publishedVersio