Standard Animal Research Articles

Genomic estimation of quantitative genetic parameters in wild admixed populations

Abstract Heritable genetic variation among free‐living animals or plants is essential for populations to respond to selection and adapt. It is therefore important to be able to estimate additive genetic variance VA, which can be obtained using a GLMM known as the animal model. An underlying assumption of the standard animal model is that the study population is genetically unstructured, which is often unrealistic. In fact, admixture might be the norm rather than the exception in the wild, like in geographically structured populations, in the presence of (im)migration or in reintroduction and conservation contexts. Unfortunately, animal model estimators may be biased in such cases. The so‐called genetic group animal models that account for genetically differentiated subpopulations have recently become popular, but methodology is currently only available for cases where relatedness among individuals can be estimated from pedigrees. To ensure that genetic group animal models with heterogeneous VA remain applicable to populations with genomic data but no pedigrees, there is a clear need to generalize these models to the case when exclusively genomic data are available. We therefore introduce such methodology for wild admixed systems by extending methods that were recently suggested in the context of plant breeding. Our extension relaxes the limiting assumptions that currently restrict their use to artificial breeding set‐ups. We illustrate the usefulness of the extended genomic genetic group animal model on a wild admixed population of house sparrows resident in an island system in Northern Norway, where genome‐wide data on more than 180,000 single nucleotide polymorphisms (SNPs) are available to derive genomic relatedness. We compare our estimates of quantitative genetic parameters to those derived from a corresponding pedigree‐based genetic group animal model. The satisfactory agreement indicates that the new method works as expected. Our extension of the very popular animal model ensures that the upcoming challenges with increasing availability of genomic data for quantitative genetic studies of wild admixed populations can be handled. To make the method widely available to the scientific community, we offer guidance in the form of a tutorial including step‐by‐step instructions to facilitate implementation.

A novel animal model of primary blast lung injury and its pathological changes in mice.

Primary blast lung injury (PBLI) is a major cause of death in military conflict and terrorist attacks on civilian populations. However, the mechanisms of PBLI are not well understood, and a standardized animal model is urgently needed. This study aimed to establish an animal model of PBLI for laboratory study. The animal model of PBLI was established using a self-made mini shock tube simulation device. In brief, mice were randomly divided into two groups: the control group and the model group, the model group were suffered 0.5 bar shock pressures. Mice were sacrificed at 2 hours, 4 hours, 6 hours, 12 hours, and 24 hours after injury. Lung tissue gross observation, hematoxylin and eosin staining and lung pathology scoring were performed to evaluated lung tissue damage. Evans blue dye leakage and bronchoalveolar lavage fluid examination were performed to evaluated pulmonary edema. The relative expression levels of inflammation factors were measured by real-time quantitative polymerase chain reaction and Western blotting analysis. The release of neutrophil extracellular traps was observed by immunofluorescence stain. In the model group, the gross observation and hematoxylin and eosin staining assay showed the inflammatory cell infiltration, intra-alveolar hemorrhage, and damaged lung tissue structure. The Evans blue dye and bronchoalveolar lavage fluid examination revealed that the lung tissue permeability and edema was significantly increased after injury. Real-time quantitative polymerase chain reaction and Western blotting assays showed that IL-1β, IL-6, TNF-α were upregulated in the model group. Immunofluorescence assay showed that the level of neutrophil extracellular traps in the lung tissue increased significantly in the model group. The self-made mini shock tube simulation device can be used to establish the animal model of PBLI successfully. Pathological changes of PBLI mice were characterized by mechanical damage and inflammatory response in lung tissue.

Hepato- and Nephro-Effect of Sphenostylis stenocarpa– Formulated Diet on Dexamethasone-Treated Pregnant Rats

This study sought to investigate the effect of Sphenostylis stenocarpa-formulated diet on hepatic and renal parameters of dexamethasone-treated pregnant rats. Sphenostylis stenocarpa were locally sourced from a market in Ado Ekiti. They were milled into powder and used in formulating feed for experimental animals. Fifteen female pregnant rats were divided in three groups of five each. Animals in group A were exposed to standard animal feed only. This served as the control group. Those in group B were exposed to Sphenostylis stenocarpa-formulated diet + 0.3 mg/kg body weight of dexamethasone, while those in group C were exposed to Sphenostylis stenocarpa-formulated diet. At the end of the eight days treatment, animals were sacrificed and blood sample, liver and kidney were collected. Exposure of pregnant rats to dexamethasone was observed to significantly (p<0.05) increased the activities of plasma aspartate amino transaminase (AST) and alanine amino transferase (ALT) as well as the concentrations of plasma total protein, bilirubin, creatinine and urea when compared with those in animals in the control as well as those fed with S. stenocarpa-formulated diet only. The results further showed that pregnant rats fed with S. stenocarpa-formulated diet only had no significant difference on plasma hepatic and renal biomarkers when compared with those in the control group. The results of liver and kidney homogenates are similar to those observed in the plasma. Exposure of animals to dexamethasone adversely unhinged hepatic and renal biomarkers investigated in the study. The study also revealed that P. biglobosa seed is beneficial to the health of the liver and kidney of pregnant female rats.

Bretschneider Solution and Two Antianginal Drugs Protect Peripheral Tissue in an Animal Model of Hemorrhagic Shock.

Shock and subsequent resuscitation provoke ischemia-reperfusion injury. Trimetazidine (TMZ), allopurinol (ALO), and histidine-tryptophan-ketoglutarate (HTK) solution, can protect from ischemia-reperfusion injury in chronic coronary syndromes and in transplantation. The objective of the current study is to compare, in a hemorrhagic shock and standard resuscitation animal model, organ damage parameters between placebo and treatment with TMZ, ALO, or HTK. Shock was induced in Wistar rats by controlled arterial bleeding, maintaining mean arterial pressure between 38 and 42 mm Hg for 60 minutes; then, drawn blood was reinfused. Animals were divided into: Sham (n = 4), Control (n = 6), TMZ (n = 7), ALO (n = 9), and HTK (n = 7). At the end of the experiment, animals were sacrificed and tissue harvested. TMZ, ALO and HTK decreased histopathologic damage in heart [Control: 1.72 (1.7-1.77); TMZ: 1.75 (1.72-1.79); ALO: 1.75 (1.74-1.8); HTK: 1.82 (1.78-1.85); all P < 0.05], kidney [Control: 3 (2-3); TMZ: 1 (1-2); ALO: 1 (1-1); HTK: 1(1-1); all P < 0.05] and intestine [Control: 3 (2-3); TMZ: 1 (1-2); ALO: 1 (1-1); HTK: 1 (0-2); all P < 0.05]. Also, treatment with TMZ, ALO, and HTK increased immunohistochemical expression of thioredoxin-1 in heart [Control: 6.6 (5.6-7.4); TMZ: 9.5 (8.1-9.7); ALO: 9.1 (8.4-10.2); HTK: 14.2 (12.6-15); all P < 0.05]; and kidney [Control: 4.6 (4-5.1); TMZ: 9.7 (9.3-9.9); ALO: 9.6 (9-9.9); HTK: 16.7 (16.1-17); all P < 0.05]. In an experimental model of hemorrhagic shock, TMZ, ALO, and HTK solution attenuated cell damage in multiple parenchyma and increased antioxidant defenses.

Economic analyses of milk production among members and non-members offarmer collectives in Saurashtra

Primary data collected for 2019-‘20 from 416 members and non-members of dairy farmer collectives (where farmers come together to market their milk collectively – this study considers a co-operative union and a milk producer company – both prominent forms of farmer collectives) in Saurashtra region of Gujarat are used to work-out the cost and returns in milk production from local cow and buffalo, and across dairy farmer categories. The analyses reveal that farmer collective organizations like co-operatives and producer companies are profitable in case of both local cow and buffalo milk production, and also for the small (1-3) and medium (3-6) herd-size category (in Standard Animal Units or SAU) of farmers. Both the overall average feed cost and Total Variable cost (TVC) per animal per day incurred by members is 12 per cent and 11 per cent less than that of non-members, respectively. Members of the co-operative receive annual bonus and members of the producer company receive annual dividends and cash incentives; with this additional benefit received by the members, their total return per litre is 25 per cent more than that of non-members. The overall average annual net returns from dairy per household for members are higher at Rs. 11,641/- compared to the returns of non-members at Rs. 3955/-. Expanding the reach of farmer collective organizations would benefit more dairy farmers by making dairy a more profitable enterprise for them.

Tumor Microenvironment and Hydrogel-Based 3D Cancer Models for In Vitro Testing Immunotherapies.

Simple SummaryImmunotherapies are emerging as promising strategies to cure cancer and extend patients’ survival. Efforts should be focused, however, on the development of preclinical tools better able to predict the therapeutic benefits in individual patients. In this context, the availability of reliable preclinical models capable of recapitulating the tumor milieu while overcoming the limitations of traditional systems is mandatory. Here, we review the tumor immune responses, escape mechanisms, and the most recent 3D biomaterial-based cancer in vitro models useful for investigating the effects of the different immunotherapeutic approaches. The main challenges and possible future trends are also discussed.In recent years, immunotherapy has emerged as a promising novel therapeutic strategy for cancer treatment. In a relevant percentage of patients, however, clinical benefits are lower than expected, pushing researchers to deeply analyze the immune responses against tumors and find more reliable and efficient tools to predict the individual response to therapy. Novel tissue engineering strategies can be adopted to realize in vitro fully humanized matrix-based models, as a compromise between standard two-dimensional (2D) cell cultures and animal tests, which are costly and hardly usable in personalized medicine. In this review, we describe the main mechanisms allowing cancer cells to escape the immune surveillance, which may play a significant role in the failure of immunotherapies. In particular, we discuss the role of the tumor microenvironment (TME) in the establishment of a milieu that greatly favors cancer malignant progression and impact on the interactions with immune cells. Then, we present an overview of the recent in vitro engineered preclinical three-dimensional (3D) models that have been adopted to resemble the interplays between cancer and immune cells and for testing current therapies and immunotherapeutic approaches. Specifically, we focus on 3D hydrogel-based tools based on different types of polymers, discussing the suitability of each of them in reproducing the TME key features based on their intrinsic or tunable characteristics. Finally, we introduce the possibility to combine the 3D models with technological fluid dynamics platforms, reproducing the dynamic complex interactions between tumor cells and immune effectors migrated in situ via the systemic circulation, pointing out the challenges that still have to be overcome for setting more predictive preclinical assays.

Comparison of a single-step with a multistep single nucleotide polymorphism best linear unbiased predictor model for genomic evaluation of conformation traits in German Holsteins

Genomic evaluation based on a single-step model uses all available data of phenotype, genotype, and pedigree; therefore, it should provide unbiased genomic breeding values with a higher correlation of prediction than the current multistep genomic model. Since 2019, a mixed reference population of cows and bulls has been applied to the routine multistep genomic evaluation in German Holsteins. For a fair comparison between the single-step and multistep genomic models, the same phenotype, genotype, and pedigree data were used. Because of its simple structure of the standard multitrait animal model used for German Holstein conventional evaluation, conformation traits were chosen as the first trait group to test a single-step SNP BLUP model for the large, genotyped population of German Holsteins. Genotype, phenotype, and pedigree data were taken from the official August 2020 conventional and genomic evaluation. Because of the same trait definition in national and multiple across-country evaluation for the conformation traits, deregressed multiple across-country evaluation estimated breeding value (EBV) of foreign bulls were treated as a new source of data for the same trait in the genomic evaluations. Due to a short history of female genotyping in Germany, the last 3 yr of youngest cows and bulls were deleted, instead of 4 yr, to perform a genomic validation. In comparison to the multistep genomic model, the single-step SNP BLUP model resulted in a higher correlation and greater variance of genomic EBV according to 798 national validation bulls. The regression of genomic prediction of the current, full evaluation on the earlier, truncated evaluation was slightly closer to 1 than the multistep model. For the validation bulls or youngest genomic artificial insemination bulls, correlation of genomic EBV between the 2 models was, on average, 0.95 across all the conformation traits. We did not find overprediction of young animals by the single-step SNP BLUP model for the conformation traits in German Holsteins.

Effect of Consumption of Sphenostylis stenocarpa Seed-formulated Diet on Oxidative Stress Biomarkers of Dexamethasone-treated Pregnant Rats

Aim: The present study tends to examine the effect of consumption of Sphenostylis stenocarpa-formulated diet on oxidative stress biomarkers of dexamethasone-treated pregnant rats.&#x0D; Methodology: Sphenostylis stenocarpa was obtained locally from a market in Ado Ekiti. They were ground into powder and used to make feed for laboratory animals. Fifteen pregnant female rats were divided into three groups of five. Animals in group A were only fed standard animal feed. This served as the control group. Those in group B were exposed to Sphenostylis stenocarpa-formulated diet + 0.3 mg/kg body weight of dexamethasone, while those in group C were exposed to Sphenostylis stenocarpa-formulated diet. At the end of the eight days treatment, animals were sacrificed and blood sample, liver and kidney were collected.&#x0D; Results: The results revealed that treatment of animals with dexamethasone significantly increased (P&lt;0.05) the activities of SOD and CAT and the concentration of MDA but decreased the concentration of GSH in plasma, liver homogenate and kidney homogenate respectively when compared with those in animals in the control group as well as those fed with S. stenocarpa-formulated diet only. The result further showed that feeding of animals with S. stenocarpa-formulated diet only had no significant effect on oxidative stress biomarkers investigated when compared with those in the control group.&#x0D; Conclusion: It can be concluded that exposure of animals to dexamethasone induced oxidative stress in animals while S. stenocarpa-formulated diet possesses the potential to alleviate the effect of oxidative stress generation.

Experimental comparative study of the effect of fractional CO2 laser combined with pulsed dye laser versus each laser alone on the treatment of hypertrophic scar of rabbit ears.

The use of fractional CO2 laser and pulsed dye laser (PDL) therapy to treat and/or prevent scarring following burn injury is becoming more widespread with a number of studies reporting reduction in scar erythema and pruritus following treatment with lasers. The objective of this study was to directly compare the efficacy of PDL, fractional CO2 , and PDL and fractional CO2 laser therapy in immature red hypertrophic scars in a standardized animal model. Ten New Zealand big-eared rabbits were used to make rabbit ear hypertrophic scar models. A total of 80hypertrophic scar models were obtained and randomly divided into groups: control (Group A), Fractional CO2 laser (Group B), pulse dye laser (Group C), combined (Group D), 20 in each group. Wound sites were treated with PDL, Fractional CO2 laser, or both at 28days post-grafting. Grafts receiving no laser therapy served as controls. Hypertrophic scar appearance, morphology, size, and erythema were assessed, and punch biopsies were collected. At days 7 and 28, additional tissue was collected for biomechanical analyses and markers for HE staining, Masson staining, immunohistochemical method to determine the CD31 content in the scar; Western blot to detect the expression of VEGF protein in scars. After the day 7 and 28, the scars were collected. Histomorphological change in scars was observed by hematoxylin-eosin staining, Masson staining. The expression of CD31, VEGF protein, and the cell apoptosis rate was detected by immunohistochemical method. (i) In morphological observation, HE staining and Masson staining, both the number of fibroblasts and amount of collagen fibrils in the experimental group were significantly reduced compared with those in control group. (ii) Micro-vessel Density (MVD) value can be found much smaller in the experimental groups than the control (p<0.05). Among the four experimental groups, there was a significant difference among 14d, 21d, and 28d groups (p<0.05). (iii) On days 7 and 28 after treatment, expression of VEGF could be regulated in experimental group (p<0.05). Among the three experimental groups, the decrease of VEGF in the combined group was significantly stronger than that of the other two. The effect of Fractional CO2 laser combined with pulsed dye laser treatment was shown to be better than that of Fractional CO2 laser or pulsed dye laser alone and inhibits the early hypertrophic scar in rabbit ears.

Effect of Tinospora cordifolia on Oxidative Stress Level Due to Drug Induced Nephrotoxicity: An Experimental Study

Introduction: Various herbs are known to confer nephroprotectivity against renal damage of different origins. Tinospora cordifolia (Willd.) Miers is known to treat kidney disorders. Yet, a lacuna of studying the protective effect of the herb on drug induced nephrotoxicity at different time periods exists. Aim: To determine the protective effect of Tinospora cordifolia (Willd.) Miers on drug induced nephrotoxic biochemical changes upon post-treatment with the herb. Material and Methods: An experimental study was carried out in Centre for Toxicology and Developmental Research, Sri Ramachandra Institute of Higher Education and Research, Chennai, Tamil Nadu, India, from September 2020 to October 2020. Gentamicin induced drug nephrotoxicity model was employed for the study. The ethanolic extract of Tinospora cordifolia was prepared. Total 51 adult male wistar rats were housed under standard animal laboratory conditions for 30 days and were assigned to four groups: Control group (Olive oil, per os), Nephrotoxicity group (Gentamicin), Toxicity cessation group (Gentamicin-Olive oil) and Post-treatment group (Gentamicin T.cordifolia ethanolic extract) groups. To induce nephrotoxicity, gentamicin (100 mg/Kg) was administered through the intraperitoneal route for 8 days. The ethanolic extract of the stem of Tinospora cordifolia (Willd.) Miers (400 mg/Kg) was administered orally for one, two and three weeks following nephrotoxicity induction. Levels of activity of Superoxide dismutase, Catalase, Glutathione Peroxidase, Reduced Glutathione contentand Lipid peroxidation in the kidney were measured. Statistical analysis was performed using One-way Analysis of Variance (ANOVA) and Post-hoc tests. Results: The reduction in superoxide dismutase (6.33±1.19 unit/ mg/mt), catalase (57.56±25.89 mcm/mt/mg ptn), glutathione peroxidase (5.79±1.87 nm/mt/mg ptn) activity, and reduced glutathione (4.98±0.31mcm/g tissue) levels and increase in the lipid peroxidation (196.28±100.05 nm/g tissue) in the kidney due to gentamicin nephrotoxicity was reversed upon post-treatment with Tinospora cordifolia (Willd.) Miers extract for 1 week (7.06±0.25 unit/mg/mt, 119.69±22.79 mcm/ mt/mg ptn, 7.08±1.73 nm/mt/mg ptn, 6.19±0.99 mcm/g tissue and 93.10±9.11 nm/g tissue), 2 weeks (7.03±0.43 unit/ mg/ mt, 181.79±39.00 mcm/mt/mg ptn, 5.07±0.81 nm/mt/mg ptn, 7.58±0.73 mcm/g tissue and 188.31±54.89 nm/g tissue) and 3 weeks (7.81±0.47 unit/mg/mt, 165.83±37.48 mcm/mt/ mg ptn, 3.92±1.87 nm/mt/mg ptn, 7.03±1.28 mcm/g tissue, 214.40±72.93 nm/g tissue). Conclusion: Post-treatment with T.cordifolia (Willd.) Miers stem extract is protective in drug induced nephrotoxic condition, even upon 1 week of administration. Its therapeutic influence on the alterations in the oxidative stress markers and antioxidant levels produced due to Gentamicin nephrotoxicity has been demonstrated.

Laboratory Codes in Nomenclature and Scientific Communication (Advancing Organism Nomenclature in Scientific Communication to Improve Research Reporting and Reproducibility)

Laboratory registration codes, also known as laboratory codes or lab codes, are a key element in standardized laboratory animal and genetic nomenclature. As such they are critical to accurate scientific communication and to research reproducibility and integrity. The original committee on Mouse Genetic Nomenclature published nomenclature conventions for mice genetics in 1940, and then conventions for inbred strains in 1952. Unique designations were needed, and have been in use since the 1950s, for the sources of animals and substrains, for the laboratories that identified new alleles or mutations, and then for developers of transgenes and induced mutations. Current laboratory codes are typically a 2- to 4-letter acronym for an institution or an investigator. Unique codes are assigned from the International Laboratory Code Registry, which was developed and is maintained by ILAR in the National Academies (National Academies of Sciences Engineering and Medicine and previously National Academy of Sciences). As a resource for the global research community, the registry has been online since 1997. Since 2003 mouse and rat genetic and strain nomenclature rules have been reviewed and updated annually as a joint effort of the International Committee on Standardized Genetic Nomenclature for Mice and the Rat Genome and Nomenclature Committee. The current nomenclature conventions (particularly conventions for non-inbred animals) are applicable beyond rodents, although not widely adopted. Ongoing recognition, since at least the 1930s, of the research relevance of genetic backgrounds and origins of animals, and of spontaneous and induced genetic variants speaks to the need for broader application of standardized nomenclature for animals in research, particularly given the increasing numbers and complexities of genetically modified swine, nonhuman primates, fish, and other species.

Effect of Parkia biglobosa seed on lipid profile of dexamethasone-treated pregnant rats

This study was aimed at evaluating the effect of Parkia biglobosa seed on dexamethasone-treated pregnant rats. Locust bean seeds were purchased from an open market in Ado Ekiti, Nigeria. It was processed and ground into powder which was subsequently used in formulating feed for experimental animals. Fifteen female pregnant rats were divided in three groups of five each. Animals in group A were exposed to standard animal feed only. This served as the control group. Those in group B were exposed to animal feed mixed with locust beans + 0.3 mg/kg body weight of dexamethasone, while those in group C were exposed to animal feed mixed with locust beans. At the end of eight days treatment, animals were sacrificed and blood sample was collected into EDTA bottles and centrifuged. Plasma was separated and used for the determination of glucose and lipid profile. Exposure of animals to dexamethasone was observed to significantly (p&lt;0.05) increased the concentration of plasma glucose concentration when compared with the control as well as animals treated with P. biglobosa only. Animals treated with dexamethasone along with P. biglobosa were observed to have higher concentrations of triglyceride, total cholesterol, low density lipoprotein (LDL) and very low density lipoprotein (VLDL) when compared with those in animals in the control group as well as those treated with P. biglobosa only. Observations from this study revealed that dexamethasone adversely perturbed and unhinged plasma glucose and lipid profile in female pregnant rats while P. biglobosa-formulated diet was observed to be a potent hypoglycemic and hypolipidemic agent.

Assessment of Parkia biglobosa on Hepatic and Renal Biomarkers of Dexamethasone-Exposed Pregnant Rats

Aim: This study sought to investigate its effect on hepatic and renal biomarkers of female pregnant rats.&#x0D; Place and Duration: This work was carried out in the Department of Medical Biochemistry and Department of Science Laboratory Technology, Ekiti State University, Ado Ekiti between January and June 2021.&#x0D; Methodology: Locust bean seeds were purchased from an open market in Ado Ekiti, Nigeria and were processed using standard method. Fifteen female pregnant rats were divided into three groups of five each. Animals in group A were exposed to standard animal feed only. This served as the control group. Those in group B were exposed to animal feed mixed with locust beans + 0.3 mg/kg body weight of dexamethasone, while those in group C were exposed to animal feed mixed with locust beans only. At the end of the eight days treatment, animals were sacrificed and blood sample, liver and kidney were collected.&#x0D; Results: Exposure of pregnant rats to dexamethasone was observed to significantly (p&lt;0.05) increased the activities of plasma aspartate amino transaminase (AST) and alanine amino transferase (ALT) as well as the concentrations of plasma total protein, bilirubin, creatinine and urea when compared with those in animals in the control as well as those treated with P. biglobosa only. The results further showed that administration of P. biglobosa only had no significant effect on plasma hepatic and renal biomarkers except urea which was significantly lower than those in the control group as well as those treated with dexamethasone. The results obtained from liver and kidney homogenate respectively are similar to those observed in the plasma.&#x0D; Conclusion: Exposure of animals to dexamethasone adversely unhinged hepatic and renal biomarkers investigated in the study. The study also revealed that P. biglobosa seed is beneficial to the health of the liver and kidney of pregnant female rats.

Sonosensitized Aggregation-Induced Emission Dots with Capacities of Immunogenic Cell Death Induction and Multivalent Blocking of Programmed Cell Death-Ligand 1 for Amplified Antitumor Immunotherapy

Sonosensitized Aggregation-Induced Emission Dots with Capacities of Immunogenic Cell Death Induction and Multivalent Blocking of Programmed Cell Death-Ligand 1 for Amplified Antitumor Immunotherapy

Factors Influencing Proteolysis and Protein Utilization in the Intestine of Pigs: A Review.

Simple SummaryIn order to minimize protein requirements and nitrogen emissions in pig production, it is important to understand the physiology of protein breakdown in the pig’s gastrointestinal tract and to find ways to improve the protein utilization efficiency of the animals. In this review, we summarize and discuss factors influencing protein degradation and thereby affecting the efficiency of the animals. We shed light on the individual pillars of protein breakdown, starting with the enzymatic breakdown of the fed protein, via the amino acid transporters absorbing in the intestine, to the proteolytic capacity of the microbial and animal-specific proteome. The available literature shows the specific activities and expression levels of proteolytic enzymes and AA transporters depending on the availability of free or bound AA in the feed. Improvements in nutrient digestibility result from changes in nutrient transporter and enzyme gene expression, as well as a change in microbial activity. We are of the opinion that in the future, also with the help of transcriptomics, more time should be invested in researching the physiology of protein degradation and the associated protein utilization efficiency using highly standardized animal trials.Pigs are among the most important farm animals for meat production worldwide. In order to meet the amino acid requirements of the animals, pigs rely on the regular intake of proteins and amino acids with their feed. Unfortunately, pigs excrete about two thirds of the used protein, and production of pork is currently associated with a high emission of nitrogen compounds resulting in negative impacts on the environment. Thus, improving protein efficiency in pigs is a central aim to decrease the usage of protein carriers in feed and to lower nitrogen emissions. This is necessary as the supply of plant protein sources is limited by the yield and the cultivable acreage for protein plants. Strategies to increase protein efficiency that go beyond the known feeding options have to be investigated considering the characteristics of the individual animals. This requires a deep understanding of the intestinal processes including enzymatic activities, capacities of amino acid transporters and the microbiome. This review provides an overview of these physiological factors and the respective analyses methods.

Low kV Computed Tomography of Parenchymal Abdominal Organs-A Systematic Animal Study of Different Contrast Media Injection Protocols.

Objectives: To evaluate multiphase low kV computed tomography (CT) imaging of the abdomen with reduced contrast media (CM) dose using different injection protocols. Methods: Two injection protocols were evaluated for use with low kV (80 kV) multiphase abdominal imaging in comparison to the standard procedure acquired at 120 kV (500 mgI/kg; 5 mL/s). This evaluation was conducted in a highly standardized animal study (5 Goettingen minipigs). The low kV protocols consisted of (a) a single-flow (SF) injection with 40% reduced CM dose and injection rate (300 mgI/kg; 3 mL/s) and (b) a DualFlow (DF) injection protocol consisting of 60%/40% contrast to saline ratio administered at 5 mL/s. Dynamic CT was first performed within representative liver regions to determine optimal contrast phases, followed by evaluation of the three protocols in multiphase abdominal CT imaging. The evaluation criteria included contrast enhancement (CE) of abdominal organs and vasculature. Results: The 80 kV DF injection protocol showed similar CE of the abdominal parenchymatous organs and vessels to the 120 kV reference and the 80 kV SF protocol. Hepatic parenchyma showed comparable CT values for all contrast phases. In particular, in the portal venous parenchymal phase, the 80 kV DF protocol demonstrated higher hepatic parenchymal enhancement; however, results were statistically non-significant. Similarly, CE of the kidney, pancreas, and abdominal arterial/venous vessels showed no significant differences between injection protocols. Conclusions: Adapted SF and DF injection protocols with reduced IDR/iodine load offer the potential to calibrate optimal CM doses to the tube voltage in abdominal multiphase low kV CT imaging. The data suggest that the DF approach allows the use of predefined injection protocols and adaption of the contrast to saline ratio to an individualized kV setting and yields the potential for patient-individualized CM adaption.

Passive immunotherapy using chicken egg yolk antibody (IgY) against diarrheagenic E. coli: A systematic review and meta-analysis

BackgroundAnimal diarrhea due to diarrheagenic Escherichia coli (E. coli) has been a major concern in the field of livestock farming leading to a severe loss of domesticated animals. This systematic review aims to analyze medical shreds of evidence available in the literature and to discover the effect of IgY in treatment and protection against E. coli diarrhea. Methods and resultsResearch reports that aimed to evaluate the effect of IgY against E. coli diarrhea were searched and collected from several databases (Science Direct, Springer link, Wiley, T&F). The collected studies were screened based on the inclusion criteria. 19 studies were identified and included in the meta-analysis. The pooled relative risk ratios were calculated for the studies and found to be statistically significant to support the therapeutic effect of IgY against E. coli diarrhea but the 95% confidence interval of a majority of studies includes a relative risk of 1. This variability between the effect of IgY in the overall estimate and individual studies accounts due to the presence of methodological heterogeneity. In addition, subgroup analysis revealed the grounds for heterogeneity. ConclusionsThis systematic review and meta-analysis provide concrete evidence for the favorable effect of IgY as a prophylactic and therapeutic modality against E. coli diarrhea. Yet, more research pieces of evidence with standardized animal studies aimed to utilize IgY against E. coli are vital. Further studies and trials on human subjects could open new perspectives in the application IgY as a therapeutic agent.

The role of serotonergic and catecholaminergic systems for possible antidepressant activity of apigenin

Background and objectiveAlthough, the anti-depressant like effects of apigenin (APG) are documented in the literature, the underlying mechanism for exerting such an effect is still not clear. In this research, an attempt was made to determine the possible role of APG for antidepressant activity through serotonergic and catecholaminergic systems using standardized animal models. Materials and methodsThe antidepressant property of APG was determine by involving tail suspension (TST) and modified forced swimming tests (MFST). The effect of APG was evaluated at 25 and 50 mg/kg. In mechanistic models, animals were pretreated with catecholaminergic and serotonergic antagonists prior to administration of APG. The results obtained were statistically analyzed to determine the level of significance. ResultsThe period of immobility in both models (TST and MFST) was significantly reduced by APG (25 and 50 mg/kg). The best therapetuic dose of APG (50 mg/kg) was selected for the mechanistic study. The anti-immobility effect of APG declined to a significant extent upon pretreatment with catecholaminergic antagonists (α-methyl-para-tyrosine methyl ester; SCH 23390; sulpiride; phentolamine) and serotonergic inhibitors (p-clorophenylalanine-methyl-ester; ondansetron) in both TST and MFST models. The antidepressant benefits of apigenin were only modestly reversed when rats were given propranolol. ConclusionsThe findings suggest that APG's antidepressant effect is mediated by the α-adrenergic, dopaminergic and 5-HT3 serotonergic receptors.

Effects of Imidacloprid on Histology and mRNA Levels of HSP70 and CYP1A Gene to a Standard Non-targeted Test Animal, Cyprinus carpio

Background: Imidacloprid (IMI) belongs to the class of neuro active insecticides, used to control pest and insects in agricultural crops. Reports suggest that IMI has highly toxic consequences on bees, humans and non-targeted aquatic animals. Hence the present study aims to investigate the toxicity effects of commercial-grade Imidacloprid (IMI) (Premise, 30.5%, a.i) using histological and transcriptional changes in heat shock protein 70 (HSP70) and cytochrome P4501A(CYP1A) genes in liver and gills of non-targeted aquatic animal, Cyprinus carpio. Methods: Three different sublethal concentrations of IMI (T1=26.04 mg/L, T2= 20.38 mg/L, T3=17.36 mg/L) were selected and common carp fingerlings were exposed for 28 days where histological alterations and expression study of HSP70 and CYP1A in gills and liver of exposed fishes being studied on 7, 14, 21 and 28 days interval using standard procedure. Result: Marked histological alteration like hydropic degeneration and cellular infiltration in liver; telangiectasis in secondary lamellae, epithelial lifting and oedema in gills were recorded. Moreover, significant upregulation of HSP70 and CYP1A gene in the gills and liver in a dose and time dependent manner was observed (P less than 0.05). As a result of the current investigation, it is obvious that IMI could be a possible toxicant that affects fish at the tissue and gene level in dosage and time dependent ways, potentially influencing other physiological processes in the long term.

Recent progress in cytometric technologies and their applications in ecotoxicology and environmental risk assessment.

Environmental toxicology focuses on identifying and predicting impact of potentially toxic anthropogenic chemicals on biosphere at various levels of biological organization. Presently there is a significant drive to gain deeper understanding of cellular and sub-cellular mechanisms of ecotoxicity. Most notable is increased focus on elucidation of cellular-response networks, interactomes, and greater implementation of cell-based biotests using high-throughput procedures, while at the same time decreasing the reliance on standard animal models used in ecotoxicity testing. This is aimed at discovery and interpretation of molecular pathways of ecotoxicity at large scale. In this regard, the applications of cytometry are perhaps one of the most fundamental prospective analytical tools for the next generation and high-throughput ecotoxicology research. The diversity of this modern technology spans flow, laser-scanning, imaging, and more recently, Raman as well as mass cytometry. The cornerstone advantages of cytometry include the possibility of multi-parameter measurements, gating and rapid analysis. Cytometry overcomes, thus, limitations of traditional bulk techniques such as spectrophotometry or gel-based techniques that average the results from pooled cell populations or small model organisms. Novel technologies such as cell imaging in flow, laser scanning cytometry, as well as mass cytometry provide innovative and tremendously powerful capabilities to analyze cells, tissues as well as to perform in situ analysis of small model organisms. In this review, we outline cytometry as a tremendously diverse field that is still vastly underutilized and often largely unknown in environmental sciences. The main motivation of this work is to highlight the potential and wide-reaching applications of cytometry in ecotoxicology, guide environmental scientists in the technological aspects as well as popularize its broader adoption in environmental risk assessment.