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Postmortem interval estimation based on protein analysis and marker studies in different organs in vivo
Abdullah M K Albloshi1, Mohamed F El-Refaei2,3,4, Eman A A Abdallah1,5
1Faculty of Medicine, Al-Baha University, Al-Baha, Kingdom of Saudi Arabia.
Estimating the postmortem interval (PMI) is challenging. This study shows protein analysis, specifically β-catenin and Bcl-2 levels in rat organs, alongside histopathology, can help determine time of death more accurately.
Area of Science:
- Forensic Science
- Biochemistry
- Pathology
Background:
- Accurate postmortem interval (PMI) estimation is vital in forensic investigations.
- Current methods for determining time of death face significant challenges in forensic medicine.
- Protein analysis and histopathology offer potential avenues for improved PMI assessment.
Purpose of the Study:
- To evaluate the utility of protein analysis and histopathological examination for estimating the postmortem interval (PMI).
- To assess changes in specific protein expressions (β-catenin and Bcl-2) in rat organs over time postmortem.
- To correlate histopathological degradation patterns with increasing PMI.
Main Methods:
- Fifty male rats were divided into five groups and organs (kidneys, liver) were collected at 0, 24, 48, 72, and 96-hour intervals postmortem.
- Immunohistochemical analysis was performed for β-catenin expression.
- Flow cytometry was used to measure Bcl-2 expression.
- Histopathological examination of liver and kidney tissues was conducted.
Main Results:
- β-catenin immunoreactivity increased significantly from 0 to 96 hours postmortem in both organs.
- Bcl-2 expression in the liver and kidney decreased over the 96-hour postmortem period.
- Histopathological analysis revealed progressive tissue degradation and loss of normal architecture in liver and kidney tissues with increasing PMI.
Conclusions:
- Alterations in specific protein autolysis, such as β-catenin and Bcl-2, show potential as diagnostic markers for PMI estimation.
- Autolytic processes demonstrate a delayed onset and accelerated progression rate.
- Organ-specific differences in autolysis rates exist, influenced by tissue structure and enzymatic content, warranting further investigation for human application.
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