Introduction

Haemonchus spp. are considered the most important strongylid nematodes with a worldwide distribution. The parasite’s blood-sucking nature can lead to severe anemia in infected animals. Despite its widespread impact, there is a dearth of comprehensive data on morphological and molecular identification methods for Haemonchus spp. in sheep from Upper Egypt. To address this gap, our current study aimed to assess the prevalence of Haemonchus spp. in 400 sheep fecal samples.

Methods

We employed microscopic examination and molecular techniques, using polymerase chain reaction (PCR) targeting the 18S gene for precise identification. Additionally, the potential risk factors associated with the infection by the parasite in sheep were explored.

Results

The study pointed out that 33.00% (132 of 400) of the examined sheep were infected with Haemonchus spp. Sheep age and seasonal variability were found to be significant factors (p < 0.05) associated with the infection. Notably, sheep under 2 years old exhibited a higher risk, with an infection rate of 43.75% (84 out of 192), than their older counterparts. Furthermore, all reported infections were exclusively observed during the cold season, constituting 58.93% (132 out of 224) of cases. By contrast, no statistically significant association (p > 0.05) was found between the sex of the examined sheep and the occurrence of haemonchosis. Employing molecular methods, we isolated and identified the parasite through PCR analysis of cultured larvae, which were then subsequently confirmed as Haemonchus contortus via phylogenetic analysis.

Blood parasites pose a significant threat to livestock production in southern Egypt, yet there is a scarcity of information regarding their circulation and epidemiology in sheep in this region. This study aimed to investigate the seroprevalence of blood parasite infections in sheep in Assiut governorate, Upper Egypt.

Monkeypox, lately known as mpox, is a zoonotic viral disease leading to an illness like smallpox in humans, but with lower mortality rates. Usually, the disease lasts between two and four weeks and occasionally results in death. The mpox virus (MPXV) is critical because it is widespread in Western and Central Africa and has spread throughout the Western Hemisphere due to international travel and the exotic pet trade. Mpox is now clinically significant due to the elimination of smallpox and the ensuing decline in vaccination efforts. Concern over the emergence of the human MPXV and its occasionally severe clinical manifestations has grown recently. The importation of diseased dogs to commercialize them as pet animals caused an outbreak of the MPXV in the United States of America. This heightened awareness of the potential for this disease to spread over the globe, either as a component of biological weapons in terrorist operations or as a result of the practice of importing wild animals as exotic pets. This review briefly describes the history, etiological agent, mode of transmission, clinical symptoms, diagnosis, treatment, and management of mpox, as well as vaccination and prevention of the disease.

Abstract

In aquaculture, improper and illogical antibiotic use could yield negative outcomes. Therefore, this study investigates the ameliorative effects of chitosan (CS) and chitosan nanoparticles (CSNPs) against the toxicity of the antibiotic doxycycline in Nile tilapia fish. The fish were divided into four distinct categories: the first group served as the control, the second group was subjected to doxycycline (40 mg/L), the third group experienced doxycycline (40 mg/L) and CS (0.5% in fish diet), and the fourth group was exposed to doxycycline (40 mg/L) with CSNPs (0.5% in fish diet) for 15 days. Levels of creatinine, uric acid, and aspartate aminotransferase activities notably elevated (p < 0.05) in the doxycycline-treated group when compared with the control group. Meanwhile, fish in the doxycycline-exposed group demonstrated significantly lower (p < 0.05) levels of red blood cells, hemoglobin, packed cell volume, mean corpuscular hemoglobin, mean corpuscular hemoglobin concentration, and neutrophils. Conversely, mean corpuscular volume, platelets, white blood cells, and lymphocytes exhibited notably higher (p < 0.05) levels in the doxycycline group. Other hematological indicators, including monocytes and eosinophils, showed no notable variances (p > 0.05) among the studied groups. Fish treated with doxycycline exhibited notably higher (p < 0.05) interleukin-1β and interleukin-6 activity in comparison to the control group. Additionally, histopathological changes were detected in the gills, liver, and kidney tissues of doxycycline-exposed fish when contrasted with the control group. Co-exposure of CS and CSNPs significantly restored most hematological, biochemical, and immunological parameters, as well as histopathological indices, in the fish, aligning these values closer to those observed in the control group in comparison to the fish treated solely with doxycycline. In conclusion, both CS and CSNPs played an important role in moderating the negative effects of doxycycline on fish, through improving hematological indices, reductions in creatinine, uric acid, and aspartate aminotransferase activity, as well as anti-inflammatory action through reductions in interleukin-1β and interleukin-6 activity.

Gastric ulceration is a common gastrointestinal ailment with serious consequences that can lead to serious illness or even death. This study aimed to examine the efficacy of tadalafil (TAD) and dexlansoprazole (DLP) in treating stomach ulcers caused by dexamethasone (DEX) in male albino Wister rats. Thirty male albino Wister rats were divided into 5 groups (6 rats each): control group received normal saline, positive control group received DEX 5 mg/kg/day intraperitoneal (i.p.) for 7 days, the third group received DLP 30 mg/kg/day orally after DEX, the fourth group received TAD 5 mg/kg/day orally after DEX, and the fifth group received DLP and TAD orally after DEX. Persistence and prevention of ulcers, pepsin activity, mucin content, and histopathological changes were evaluated after each trial. Reduced glutathione (GSH), nitric oxide (NO), and malondialdehyde (MDA) levels were measured in gastric homogenates. Serum levels of prostaglandin E₂ (PGE₂), tumor necrosis factor-α (TNF-α), and interleukin-10 (IL-10) were also measured.  Treatment with either TAD or DLP alone significantly reduced ulcer index (U.I.), pepsin activity, TNF-α, IL-10 and MDA with significant rise in mucin content, PGE₂, NO, GSH, and improved the histological alteration compared to DEX group. When TAD and DLP were administered together, there was a more notable decrease in U.I., pepsin activity, gastric MDA, TNF-α, and IL-10 with concomitant more significant increase in mucin content, NO content, and PGE₂ production compared to the TAD or DLP groups alone. Compared to each medicine alone, TAD and DLP together have promising therapeutic potential in preventing stomach ulcers caused by DEX.

Abstract

Background

Acute liver failure (ALF) is a critical condition characterized by rapid liver dysfunction, leading to high mortality rates. Current treatments are limited, primarily supportive, and often require liver transplantation. This study investigates the potential of a novel nanoparticle formulation of glutathione (GSH) and virgin coconut oil (VCO) alone and in combination to enhance therapeutic outcomes in a rat model of ALF induced by orogastric carbon tetrachloride (CCl₄).

Methods

The study employed adult male Albino rats divided into ten groups, with ALF induced via a single oral dose of CCl₄. Various treatment regimens were administered over seven days, including conventional and nanoparticle forms of GSH and VCO and their combinations. The efficacy of treatments was evaluated through biochemical analysis of liver function markers, oxidative stress indicators, inflammatory biomarkers, and histopathological examinations. Nanoparticles were synthesized using established methods, and characterization techniques were employed to ensure their quality and properties.

Results

The nanoparticle formulations significantly improved liver function, as indicated by reduced serum levels of alanine aminotransferase and aspartate aminotransferase, alongside decreased oxidative stress markers such as malondialdehyde. Furthermore, they reduced tumor necrosis factor alpha and interleukin-1 beta inflammatory markers. Histological analysis revealed reduced hepatocellular necrosis and inflammation in treated groups compared to controls. Also, decreased nuclear factor-kappa B was detected by immunohistochemical analysis.

Conclusion

The findings show that the nanoparticle mixture of GSH and VCO effectively reduces liver damage in ALF. This suggests a promising drug-based approach for improving liver regeneration and protection. This innovative strategy may pave the way for new therapeutic interventions in the management of ALF.