Pozitivan učinak L-karnitina na imuno- metabolički odgovor i antioksidacijski status u koza s gravidnosnom toksemijom

According to the literature, there have been limited studies describing the efficacy of L-carnitine (LC) administration in goats. The present study was designed to evaluate the influence of orally administered LC on some immune- metabolic variables, as well as the redox status in goats with experimentally induced pregnancy toxemia (PT). The study included eighteen clinically healthy Baladi goats at 110 ± 5 days of gestation. The animals were randomly allocated into three equally-sized groups: control, toxemic (PT), and toxemic treated with LC (TLC). On day 110 ± 5 of gestation, the goats in the TLC group received 10 mL of LC given as an oral drench once daily. Administration of LC was continued for 20 consecutive days. At day 130 of gestation, PT was experimentally induced in the animals of the PT and TLC groups by means of feed withdrawal for 72 hours. For biochemical analyses, blood samples were collected from each investigated doe via jugular vein puncture before PT induction (T0), and once daily for five consecutive days (T1, T2, T3, T4, and T5). The clinical findings of PT appeared in all the goats of the PT group after 72 hours of feed withdrawal, while the goats of the TLC group did not show any clinical symptoms throughout the study period. Administration of LC elicited initial and sustained low serum levels of malondialdehyde (MDA), tumor necrosis factor (TNF-α), and high serum glucose, superoxide dismutase (SOD) and interleukin (IL)-10 at T0 compared with those of the control and PT groups. At T3, goats that received LC showed significantly lower values of β-hydroxybutyric acid, non-esterified fatty acid, triacylglycerols, MDA, TNF-α, IL-1β, IL-6, and higher values of total cholesterol, glutathione peroxidase, SOD, and IL-10 than those of the PT group. Our data suggest that orally administered LC could be useful in ameliorating the immune status and improving lipid metabolism in goats with PT.Prema podacima iz literature postoji ograničen broj istraživanja primjene L-karnitina (LK) u koza. Cilj ovog rada bio je procijeniti učinak oralno primijenjenog LK-a na određene imuno-metaboličke pokazatelje i redoksni status u koza u kojih je eksperimentalno izazvana gravidnosna tokesmija (GT). Istraživanje je uključilo 18 klinički zdravih koza baladi pasmine čija je gravidnost iznosila 110 ± 5 dana. Životinje su nasumično podijeljene u tri jednake skupine: kontrolnu, toksemijsku (GT) i toksemijsku kojoj je davan LK (TLK). Koze u skupini TLK su od 110. ± 5 dana gravidnosti jedanput dnevno dobivale 10 mL LK-a oralnom drenčer špricom. Primjena LK-a nastavljena je sljedećih dvadeset dana uzastopno. Na 130. dan gravidnosti GT je eksperimentalno izazvan u skupinama GT i TLK, uz uskraćivanje hrane tijekom 72 sata. U svake je koze iz jugularne vene uzeta krv za biokemijsku analizu prije izazivanja GT-a (T0) i jedanput dnevno sljedećih pet dana (T1, T2, T3, T4 i T5). Klinički je GT ustanovljen u svih koza u skupini GT 72 sata nakon što im je uskraćena hrana, dok koze iz skupine TLK nisu pokazale kliničke simptome za vrijeme istraživanja. Primjena LK-a prouzročila je niske serumske vrijednosti malondialdehida (MDA), faktora tumorske nekroze (TNF-α) i visoke serumske vrijednosti glukoze, superoksidne dismutaze (SOD) i interleukina (IL)- 10 prije izazivanja GT-a (T0) u usporedbi s kontrolnom i GT skupinom. Treći dan (T3) koze koje su primile LK pokazale su znakovito niže vrijednosti β-hidroksimaslačne kiseline, neesterificirane masne kiseline, triacilglicerola, MDA-a, TNF-α, IL-1β, IL-6 te veće vrijednosti ukupnog kolesterola, glutation-peroksidaze, SOD-a i IL-10 od onih u skupini GT. Rezultati su pokazali da bi oralno primijenjen LK mogao pridonijeti poboljšanju imunosnog statusa i metabolizma masnoća u koza s GT-om

Chemistry and biological activities of the marine sponges of the genera mycale (Arenochalina), Biemna and Clathria

Over the past seven decades, particularly since the discovery of the first marine-derived nucleosides, spongothymidine and spongouridine, from the Caribbean sponge Cryptotethya crypta in the early 1950s, marine natural products have emerged as unique, renewable and yet under-investigated pools for discovery of new drug leads with distinct structural features, and myriad interesting biological activities. Marine sponges are the most primitive and simplest multicellular animals, with approximately 8900 known described species, although more than 15,000 species are thought to exist worldwide today. These marine organisms potentially represent the richest pipeline for novel drug leads. Mycale (Arenochalina) and Clathria are recognized marine sponge genera belonging to the order Poecilosclerida, whereas Biemna was more recently reclassified, based on molecular genetics, as a new order Biemnida. Together, these sponge genera contribute to the production of physiologically active molecular entities with diverse structural features and a wide range of medicinal and therapeutic potentialities. In this review, we provide a comprehensive insight and up-to-date literature survey over the period of 1976–2018, focusing on the chemistry of the isolated compounds from members of these three genera, as well as their biological and pharmacological activities, whenever available. © 2018 by the authors.Acknowledgments: This work was supported by the mission sector of the Ministry of High Education of the Arab Republic of Egypt (Egyptian cultural bureau in Paris and Athens); Amr El-Demerdash’s, and Mohamed Tammam’s joint supervision were fully funded and supported

Impact of Genetic Polymorphism of Myeloid Differentiation Primary Response Gene 88, Enhancer of Zeste Homolog 2, and B-cell Lymphoma 2 like 11 in Patients with Diffuse Large B Cell Lymphoma Treated with Rituximab, Cyclophosphamide, Doxorubicin, Vincristin

BACKGROUND: Despite the growing landscape of genetic drivers in Diffuse Large B-cell Lymphoma, yet their clinical implication is still unclear and R-CHOP regimen remains a “one size fits all” therapy. We aimed in this study to examine the prevalence of EZH2, BCL211 and MYD 88 genetic polymorphisms in DLBCL patients and correlate the results with various clinical and survival outcomes. METHODS: Genotyping of MYD88 (rs387907272 T/C), EZH2 (rs3757441 C/T), and BCL2L11 (rs3789068 A/G) polymorphisms were conducted using real time polymerase chain reaction analysis in a total of 75 DLBCL patients. RESULTS: Most of our cases carried the wild TT genotype of MYD88 gene (64%), the mutant TT genotype of EZH2 gene (52%) and the wild AA genotype of BCL2L11 gene (48%). Regarding cell of origin, Germinal Centre (GC) phenotype was present in 56% of cases while 44% expressed the Post-GC (PGC) phenotype. Poor response outcome to first line R-CHOP was significantly correlated with the mutated CC genotype of MYD 88 (p=0.02), while better response to R-CHOP was significantly associated with younger age <50 years (p <0.0001), good PS (p=0.046), normal LDH level (p=0.003), earlier stage (p <0.0001), good IPI score (p=0.009), absence of extranodal disease (p <0.0001) and absence of bulky disease (p=0.004). The median PFS and the 2 year OS were significantly higher in younger age, earlier stage, good IPI score, absence of extranodal disease, absence of bulky disease and in GC phenotype. CONCLUSIONS: Our results emphasized that the mutated genotype of MYD 88 gene polymorphism is significantly associated with poor response to R-CHOP therapy

Dual functions of Macpiwi1 in transposon silencing and stem cell maintenance in the flatworm Macrostomum lignano

PIWI proteins and piRNA pathways are essential for transposon silencing and some aspects of gene regulation during animal germline development. In contrast to most animal species, some flatworms also express PIWIs and piRNAs in somatic stem cells, where they are required for tissue renewal and regeneration. Here, we have identified and characterized piRNAs and PIWI proteins in the emerging model flatworm Macrostomum lignano. We found that M. lignano encodes at least three PIWI proteins. One of these, Macpiwi1, acts as a key component of the canonical piRNA pathway in the germline and in somatic stem cells. Knockdown of Macpiwi1 dramatically reduces piRNA levels, derepresses transposons, and severely impacts stem cell maintenance. Knockdown of the piRNA biogenesis factor Macvasa caused an even greater reduction in piRNA levels with a corresponding increase in transposons. Yet, in Macvasa knockdown animals, we detected no major impact on stem cell self-renewal. These results may suggest stem cell maintenance functions of PIWI proteins in flatworms that are distinguishable from their impact on transposons and that might function independently of what are considered canonical piRNA populations

Diagnostic efficacy of monoclonal antibody based sandwich enzyme linked immunosorbent assay (ELISA) for detection of Fasciola gigantica excretory/secretory antigens in both serum and stool

<p>Abstract</p> <p>Background</p> <p>This research was carried out to develop a reliable monoclonal antibody (MoAb)-based sandwich enzyme linked immunosorbent assay (ELISA) for the diagnosis of active <it>Fasciola gigantica </it>infection in both serum and stool for comparative purposes.</p> <p>Methods</p> <p>From a panel of MoAbs raised against <it>F. gigantica </it>excretory/secretory antigens (ES Ags), a pair (12B/11D/3F and 10A/9D/10G) was chosen due to its high reactivity and strict specificity to <it>F. gigantica </it>antigen by indirect ELISA.</p> <p>Results</p> <p>The two MoAbs were of the IgG₁and IgG_2asubclasses, respectively. Using SDS-PAGE and EITB, the selected MoAbs recognized 83, 64, 45 and 26 kDa bands of ES Ags. The lower detection limit of ELISA assay was 3 ng/ml. In stool, the sensitivity, specificity and diagnostic efficacy of ELISA was 96%, 98.2 and 97.1%; while in serum they were 94%, 94.6% and 94.3%, respectively. Moreover, a positive correlation was found between ova count in stool of <it>F. gigantica </it>infected patients and the OD readings of ELISA in both stool and serum samples (<it>r </it>= 0.730, p < 0.01 and r = 0.608; p < 0.01, respectively).</p> <p>Conclusions</p> <p>These data showed that the use of MoAb-based sandwich ELISA for the detection of <it>F. gigantica </it>coproantigens in stool specimens was superior to serum samples; it provides a highly efficient, non-invasive technique for the diagnosis of active <it>F. gigantica </it>infection.</p

Internet-based search of randomised trials relevant to mental health originating in the Arab world

BACKGROUND: The internet is becoming a widely used source of accessing medical research through various on-line databases. This instant access to information is of benefit to busy clinicians and service users around the world. The population of the Arab World is comparable to that of the United States, yet it is widely believed to have a greatly contrasting output of randomised controlled trials related to mental health. This study was designed to investigate the existence of such research in the Arab World and also to investigate the availability of this research on-line. METHODS: Survey of findings from three internet-based potential sources of randomised trials originating from the Arab world and relevant to mental health care. RESULTS: A manual search of an Arabic online current contents service identified 3 studies, MEDLINE, EMBASE, and PsycINFO searches identified only 1 study, and a manual search of a specifically indexed, study-based mental health database, PsiTri, revealed 27 trials. CONCLUSION: There genuinely seem to be few trials from the Arab world and accessing these on-line was problematic. Replication of some studies that guide psychiatric/psychological practice in the Arab world would seem prudent

In vivo tissue uptake of intravenously injected water soluble all-trans β-carotene used as a food colorant

Water soluble β-carotene (WS-BC) is a carotenoid form that has been developed as a food colorant. WS-BC is known to contain 10% of all-trans β-carotene (AT-BC). The aim of the present study was to investigate in vivo tissue uptake of AT-BC after the administration of WS-BC into rats. Seven-week-old male rats were administered 20 mg of WS-BC dissolved in saline by intravenous injection into the tail vein. At 0, 6, 24, 72, 120 and 168 hours (n = 7/time), blood was drawn and liver, lungs, adrenal glands, kidneys and testes were dissected. The levels of AT-BC in the plasma and dissected tissues were quantified with HPLC. After intravenous administration, AT-BC level in plasma first increased up to 6 h and returned to normal at 72 h. In the testes, the AT-BC level first increased up to 24 h and then did not decrease but was retained up to 168 h. In the other tissues, the level first increased up to 6 h and then decreased from 6 to 120 or 168 h but did not return to normal. The accumulation of WS-BC in testes but not in the other 5 tissues examined may suggest that AT-BC was excreted or metabolized in these tissues but not in testes. Although WS-BC is commonly used as a food colorant, its effects on body tissues are still not clarified. Results of the present study suggest that further investigations are required to elucidate effects of WS-BC on various body tissues