Amin Mohammed

The impact of black seed oil on tramadol-induced hepatotoxicity: Immunohistochemical and ultrastructural study

The natural herb, black seed (Nigella Sativa; NS) is one of the most important elements of folk medicine. The aim was to evaluate the impact of Nigella Sativa Oil (NSO) on the changes induced by tramadol in rat liver. Twenty four albino rats were used. CONTROL GROUP given intraperitoneal and oral saline for 30days. TR-group: given intraperitoneal tramadol (20, 40, 80mg/kg/day) in the first, middle and last 10days of the experiment, respectively. TR+NS group: administered intraperitoneal tramadol in similar doses to TR-group plus oral NSO (4ml/kg/day) for 30days. Immunohistochemical, electron microscopic, biochemical and statistical studies were performed. TR-group displayed disarranged hepatic architecture, hepatic congestion, hemorrhage and necrosis. Apoptotic hepatocytes, mononuclear cellular infiltration and a significant increase in the number of anti-CD68 positive cells were observed. Ultrastructurally, hepatocytes showed shrunken nuclei, swollen mitochondria, many lysosomes and autophagic vacuoles. Activated Ito and Von Kupffer cells were also demonstrated. Elevated serum levels of AST, ALT, ALP and bilirubin were noticed. NSO administration resulted in preservation of hepatic histoarchitecture and ultrastructure and significant reductions in the number of anti-CD68 positive cells and serum levels of liver seromarkers. In conclusion, NSO administration could mitigate the alterations induced by tramadol in rat liver.

Effect of Biochanin A versus 17β estradiol in rat submandibular salivary gland

The epigenetic nature of development mandates the observation of the effect of any exogenous substance, especially those with estrogenic activities, during critical phases of development. The submandibular gland (SMG) presents as a great model due to extensive postnatal development, and is known to be regulated and affected by hormones as well as growth factors. Herein, we observed postnatal development following low doses of Biochanin A (BCA) and 17β estradiol (E2) in rats. The pups were randomly divided into four groups: control, BCA, E2, and dimethyl sulfoxide (DMSO), and euthanized at the 6th, 15th, 30th, and 60th postnatal days (PND). SMG morphogenesis was assessed. The nuclear expression of estrogen receptor beta (ERβ) was evaluated immunohistochemically; ERβ expression was up-regulated by BCA and down-regulated by E2. Similarly, caspase three gene expression, assessed by real time polymerase chain reaction was increased in the BCA group but decreased in the E2 group. A significant decrease in epidermal growth factor gene expression was noted at PND 30. The results presented by this study provide evidence that the effect of a postnatal exposure of the SMG to Biochanin A during development could be linked to sex hormone-dependent disorders.

Identification of Cyclase-Associated Protein-2 as a Novel Biomarker for Early-Stage Hepatocellular Carcinoma

Background: Hepatocellular carcinoma (HCC) is an aggressive deadly cancer with few therapeutic options mostly limited for early-stage HCC. Unfortunately, alphafetoprotein (AFP) has a limited performance, especially in early-stage HCC. Objectives: to investigate plasma levels of Cyclaseassociated protein-2 (CAP2) as a new biomarker and evaluate its role in detecting early-stage and AFP-negative HCC Egyptian patients. Methods: Plasma CAP2 and AFP levels in 150 HCC, 150 cirrhotic patients, 150 healthy controls. Correlation with tumor behavior, the area under the curve (AUC), sensitivity, specificity, and diagnostic accuracy were analyzed. Results: Plasma CAP2 and AFP levels were significantly elevated in HCC patients than liver cirrhosis and controls. Only plasma CAP2 levels significantly correlated with clinico-pathological characteristics of HCC (BCLC, histological and clinical stages) but not correlated with patients age, gender, viral infection status or AFP levels. Compared to AFP, CAP2 had significantly higher AUC: 0.86 (0.79-0.93) vs. 0.75 (0.65-0.85), Sensitivity: 81.5% vs. 62% in all HCCs and significantly higher AUC: 0.80 (0.72-0.89) vs. 0.68 (0.58-0.79, Sensitivity: 80.5% vs. 43.1% in earlystage HCC. Moreover, the combined diagnostic value of both CAP2+AFP was statistically significantly better than either CAP2 or AFP alone. Also, CAP2 could predict 82.4% of AFP-negative HCCs [AUC: 0.85 (0.77-0.92)] and 73.5% of AFP-negative early-stage HCCs [AUC: 0.80 (0.72-0.88)]. Conclusion: Compared with AFP, CAP2 was significantly elevated in HCC patients with higher sensitivity and AUC especially for early-stage HCC. Moreover, CAP2 was significantly correlated with the clinico-pathological features of HCC. CAP2 could be a novel biomarker predicting early-stage, AFP-negative, and AFP-negative early-stage HCC patients.

Immunohistochemical localization of epidermal growth factor receptors in the liver of normal and streptozotocin-induced diabetic rats

Background Diabetes mellitus is a metabolic disease characterized by hyperglycemia, which affects different tissues including the liver. Epidermal growth factor receptor (EGFR) family is one of the tyrosine kinase receptor families that regulate liver pathophysiology. Aim of the work This study aimed to demonstrate the histological and EGFR immunohistochemical changes that occur in the liver of streptozotocin (STZ)-induced diabetic rat. Materials and methods Twenty male albino rats divided into two groups, group I (control) and group II (diabetic), were used. Diabetes was induced in the animals in group II by a single intraperitoneal injection of STZ (40 mg/kg). Five rats from each group were sacrificed 2 and 4 weeks after the STZ injection. Blood samples were collected for detection of serum glucose and insulin levels. Paraffin sections of the liver were prepared and stained with H&E, periodic acid Schiff, Masson’s trichrome stains, and immunohistochemical stain using anti-EGFR antibody. Results Diabetes mellitus was associated with marked congestion of central veins, blood sinusoids, and hepatic veins. Hepatocytes showed degenerative and fatty changes, especially in the periportal regions. Four weeks after induction of diabetes, signs of hepatic regeneration such as large binucleated hepatocytes were observed in the pericentral regions. Control livers showed strong positive EGFR immunoreactivity in hepatocytes, mainly in the periportal and pericentral regions, and in the bile duct epithelium. A marked decrease in EGFR immunoreactivity was observed in the livers of diabetic rats. Conclusion Diabetes mellitus is associated with marked hepatic congestion, degenerative and fatty changes in the hepatocytes, and decreased hepatic EGFR immunoreactivity.