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      Nutritional response to water hyacinth ( Eichhornia crassipes) challenges via blood biochemical profiles in goats and sheep

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          Abstract

          Eichhornia crassipes remains a significant threat to aquatic ecosystems and poses economic challenges globally. Interestingly, its high nutritional value and abundance in water bodies, making it a promising and cost-effective source of animal feed. The purpose of the study was to see how varying inclusion rates of E. crassipise affected the blood biochemical profiles of Doyogena sheep and Woyto-Guji goat local breeds. Twelve sheep and twelve goats were used in a 2*4 randomized crossover design with two species, four diets, and four phases (15-day adaptation plus 7-day experimental diets), and on the last day blood sample collected. The dietary treatments included E. crassipise (0, 25, 50, and 75%) as a substitute for commercial concentrate. The data were analyzed using SAS software tool PROC GLM, and Pearson's correlation coefficient between serum biochemical indices was computed. Results of AST, ALB, GLB, AST/ALT, and A/G showed significant (P < 0.0001), ALP (P < 0.005), and GLU (P < 0.05) differences between species of animals, except for ALT, CREAT, TP, and UREA. Sheep had higher values for AST, ALP, GLB, AST/ALT, CREAT, and UREA, except for A/G, ALB, ALT, and TP. Among treatments and treatment species interaction effect did not show variation in all studied parameters. Positive correlations were observed between ALT and AST, TP and ALB, and A/G and ALB, negative correlations were observed between ALT and AST/ALT, TP and A/G; GLB and A/G in sheep. Furthermore, positive correlations were observed between AST/ALT with ALT and AST and ALB with TP and A/G; however, negative correlations were observed between ALB with TP and A/G in goats. It was concluded that substituting E. crassipise with concentrate had no adverse effect on the serum biochemical profile.

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          The current state of serum biomarkers of hepatotoxicity.

          The level of serum alanine aminotransferase (ALT) activity reflects damage to hepatocytes and is considered to be a highly sensitive and fairly specific preclinical and clinical biomarker of hepatotoxicity. However, an increase in serum ALT activity level has also been associated with other organ toxicities, thus, indicating that the enzyme has specificity beyond liver in the absence of correlative histomorphologic alteration in liver. Thus, unidentified non-hepatic sources of serum ALT activity may inadvertently influence the decision of whether to continue development of a novel pharmaceutical compound. To assess the risk of false positives due to extraneous sources of serum ALT activity, additional biomarkers are sought with improved specificity for liver function compared to serum ALT activity alone. Current published biomarker candidates are reviewed herein and compared with ALT performance in preclinical and on occasion, clinical studies. An examination of the current state of hepatotoxic biomarkers indicates that serum F protein, arginase I, and glutathione-S-transferase alpha (GSTalpha) levels, all measured by ELISA, may show utility, however, antibody availability and high cost per run may present limitations to widespread applicability in preclinical safety studies. In contrast, the enzymatic markers sorbitol dehydrogenase, glutamate dehydrogenase, paraxonase, malate dehydrogenase, and purine nucleoside phosphorylase are all readily measured by photometric methods and use reagents that work across preclinical species and humans and are commercially available. The published literature suggests that these markers, once examined collectively in a large qualification study, could provide additional information relative to serum ALT and aspartate aminotransferase (AST) values. Since these biomarkers are found in the serum/plasma of treated humans and rats, they have potential to be utilized as bridging markers to monitor acute drug-induced liver injury in early clinical trials.
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            Equilibrium and kinetic models on the adsorption of Reactive Black 5 from aqueous solution using Eichhornia crassipes /chitosan composite

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              Biochemical and hematologic reference intervals for free-ranging desert bighorn sheep.

              Over 200 clinically normal desert bighorn sheep (Ovis canadensis) from multiple geographic areas were sampled utilizing a uniform protocol. The goals of this study were to develop comprehensive reference intervals for hematologic and biochemical analytes using central 90th percentile nonparametric analyses. Adult female sheep had greater erythrocyte mass (hemoglobin and hematocrit) compared with adult male sheep. Young animals < or = 1-yr-old had greater erythrocyte mass (hemoglobin, hematocrit and red blood cell count), higher alkaline phosphatase activity, and lower serum protein and globulin concentrations compared with adult animals. Because of the large sample size, wide geographic range, and uniform sample and handling protocol in this study, these reference intervals should be robust and applicable to other free-ranging desert bighorn sheep populations.
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                Author and article information

                Contributors
                Journal
                Heliyon
                Heliyon
                Heliyon
                Elsevier
                2405-8440
                26 March 2024
                15 April 2024
                26 March 2024
                : 10
                : 7
                : e28424
                Affiliations
                [a ]Department of Animal and Range Sciences, College of Agriculture, Wolaita Soddo University, P. O. Box 138, Wolaita Sodo, Ethiopia
                [b ]Department of Animal Sciences, College of Agricultural Sciences, Arba Minch University, P. O. BOX 21, Arba Minch, Ethiopia
                Author notes
                [* ]Corresponding author. Department of Animal and Range Sciences, College of Agriculture, Wolaita Soddo University, P. O. Box 138, Wolaita Sodo, Ethiopia. yfanta2017@ 123456gmail.com
                Article
                S2405-8440(24)04455-4 e28424
                10.1016/j.heliyon.2024.e28424
                11059523
                38689994
                b5a29fe9-f8d6-40fa-8b5f-ac502c70d187
                © 2024 The Authors

                This is an open access article under the CC BY-NC license (http://creativecommons.org/licenses/by-nc/4.0/).

                History
                : 6 November 2023
                : 14 March 2024
                : 19 March 2024
                Categories
                Research Article

                biochemical profile,doyogena sheep,eichhornia crassipes,woyto-guji goat

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