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Khasawneh, R.

Publications and source records attributed to Khasawneh, R..

2 recordsLinked to original sources

Combining Low toxic dose Tramadol and smoking is relatively safe unless you stop them: An Animal model evidence of Endoplasmic reticulum stress

Low toxic doses of tramadol induced animal brain cortex apoptosis and hippocampus injury. Adding nicotine reverted hippocampus pathological changes without triggering brain injury. The expression of CHOP protein in real-time PCR showed mild Endoplasmic reticulum stress (ER) in rats brains. Histological, immunohistochemical, and western blotting analysis of CHOP and BIP chaperones demonstrated Endoplasmic reticulum stress in brain and liver tissue samples. Furthermore, the levels of apoptosis and autophagy markers demonstrated a mild increase. Adding Nicotine relatively decreasedbrain and liver ER stress. The combined profile was considerably protective in comparison to administering each drug separately. Mild ER stress is essential for normal cell functions. The blood level of serotonin was high in all study groups with a marked increase in its level when tramadol and nicotine were combined. Low toxic doses of tramadol in combination with nicotine were safe at the reproductive system level which was evaluated by histological examination and animal blood androgen assay. Generally, combining low-dose tramadol with smoking was found to be safe in various animal tissues and organs, however, the high serotonin level in the blood can be critical and associated with a high risk of serious withdrawal and pathological consequences. Serotonin receptor blockers such as olanzapine may increase systemic serotonin levels and need further investigation to utterly pinpoint their roles in managing mood disorders.

pharmacology and toxicology↗

Pax9 is required for cardiovascular development and interacts with Tbx1 in the pharyngeal endoderm to control 4th pharyngeal arch artery morphogenesis.

Developmental defects affecting the heart and aortic arch arteries are a key phenotype observed in DiGeorge syndrome patients and are caused by a microdeletion on chromosome 22q11. Heterozygosity of TBX1, one of the deleted genes, is expressed throughout the pharyngeal arches and is considered a key component for the arch artery defects. Pax9 is expressed in the pharyngeal endoderm and is downregulated in Tbx1 mutant mice. We show here that Pax9 deficient mice are born with complex cardiovascular malformations affecting the outflow tract and aortic arch arteries with failure of the 3rd and 4th pharyngeal arch arteries to form correctly. Transcriptome analysis indicated that Pax9 and Tbx1 may function together, and mice double heterozygous for Tbx1/Pax9 presented with a significantly increased incidence of interrupted aortic arch when compared to Tbx1 heterozygous mice. Using a novel Pax9Cre allele we demonstrated that the site of this Tbx1-Pax9 genetic interaction is in the pharyngeal endoderm, therefore revealing that a Tbx1/Pax9-controlled signalling mechanism emanating from the pharyngeal endoderm is required for critical tissue interactions during normal morphogenesis of the pharyngeal arch artery system.\n\nSummary statementPax9 is required for outflow tract and aortic arch development, and functions together with Tbx1 in the pharyngeal endoderm for 4th arch artery formation.

developmental biology↗