MOLECULAR VERSUS HISTOPATHOLOGICAL EXAMINATION OF THE PROSTATE GLAND IN THE ESTIMATION OF POST-MORTEM INTERVAL (AN EXPERIMENTAL STUDY) | ||
| The Egyptian Journal of Forensic Sciences and Applied Toxicology | ||
| Article 3, Volume 18, Issue 1, May 2018, Pages 35-54 PDF (1.86 M) | ||
| Document Type: Original Article | ||
| DOI: 10.21608/ejfsat.2018.28293 | ||
| Abstract | ||
| After death, multiple alterations of biochemical and pathological processes originate resulting in considerable disturbance of the structure and composition of the human body. These changes occur in a sequential manner that may enable estimation of post-mortem interval (PMI). As prostate is the most resistant organ to decomposition, its post mortem histopathological changes as well as pattern of DNA degradation may be useful for PMI determination. This study aimed to investigate the PMI by histopathological examination of the prostate versus its DNA degradation rate in adult male albino rats. Methodology: One hundred and four albino rats were implemented in the study. They were divided into 4 groups (according to the chosen post mortem interval). Group I (early PMI): rats were subdivided into 6 equal subgroups; Group (Ia), (Ib), (Ic), (Id), (Ie) and (If) were examined at PMIs of (zero, 3, 6, 9, 12 and 24 hours, respectively). Group II (intermediate PMI): rats were subdivided into 3 equal subgroups: Group (IIa), (IIb) and (IIc) were examined at PMIs of (2, 4 and 6 days, respectively). Group III (delayed PMI): rats were subdivided into 4 equal subgroups: Group (IIIa), (IIIb), (IIIc) and (IVd) rats were examined at PM interval of (1, 2, 3 and 4 weeks, respectively). Experimental parameters: Prostate was dissected, divided into two portions and left at room temperature. At each scheduled post mortem interval one portion was prepared for light microscopic examination. The other portion was subjected to DNA extraction and agarose gel electrophoresis. Results: light microscopic examination of prostate samples didn't detect any structure abnormality during the first twelve hours post mortem (PM). Twenty-four hours PM significant epithelial disruption, inflammatory cells and fatty degeneration began to appear in the prostatic acini. Two days PM, the prostatic acini showed significant atrophy and necrosis. By six days PM, stromal calcification started to appear. One week to four weeks PM, the prostatic acinar epithelial disruption, atrophic acini, necrosis and stromal calcification became extensive till no more normal glandular or fibromuscular architecture can be detected. The results of extracted glandular DNA showed that DNA resisted the degradation up to twenty-four hours PM. Thereafter, PM degradation patterns progressed to small pieces of low molecular weight DNA less than 400 bp detected at six days PM then to more degraded DNA to reach less than 100 bp at three weeks PM. Four weeks PM, there was complete disappearance of small fragmented molecules. According to the results of this study, it can be concluded that histopathological changes as well as DNA degradation of the prostate were sequential PM processes that are time based. So, they may be used as a predictor of PMI. The slower degeneration of prostate DNA offers a preferable tool for forensic studies at delayed PMI than the histopathological examination of the same organ. | ||
| Keywords | ||
| prostate; Post mortem interval –DNA | ||
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