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Updated: Aug 19, 2026

Lavage-induced Surfactant Depletion in Pigs As a Model of the Acute Respiratory Distress Syndrome (ARDS)
Published on: September 7, 2016
A quantitative RT-PCR assay of surfactant-associated protein A1 and A2 mRNA transcripts as a diagnostic tool for
Kaori Ishida1, Bao-Li Zhu, Hitoshi Maeda
1Department of Legal Medicine, Osaka City University Medical School, Abeno, Japan. ishida@med.osaka-cu.ac.jp
Abstract:
Although an immunohistochemical investigation of pulmonary surfactant-associated protein A (SP-A) suggested a characteristic increase in fatal asphyxiation, no particular change was observed in the total amount of SP-A mRNA. SP-A is encoded by two highly similar genes, SP-A1 and SP-A2, which are differentially regulated in the expression. In the present study, to investigate the molecular pathology of SP-A, we established a method for quantitative RT-PCR assay of SP-A1 and SP-A2 mRNA transcripts. Using this method, fatalities from acute mechanical asphyxia (n=12) and drowning (n=9) were examined in comparison with control groups (n=17) of acute myocardial infarction (n=11) and peracute death due to brain lacerations (n=6). The SP-A1/A2 ratio (mean value) was markedly elevated in mechanical asphyxia (6.72) and drowning (5.64), whereas it was low in controls (acute myocardial infarction, 2.80; brain lacerations, 2.56). The analysis of the SP-A1/A2 ratio may assist interpretation of the molecular alterations of SP-A related to acute asphyxial death.
Insights
The ratio of surfactant protein A (SP-A) gene transcripts, SP-A1 and SP-A2, is significantly elevated in deaths from mechanical asphyxia and drowning. This finding may help identify molecular changes in SP-A related to acute asphyxial fatalities.
Area of Science:
- Forensic Pathology
- Molecular Biology
- Genetics
Background:
- Pulmonary surfactant-associated protein A (SP-A) shows increased levels in fatal asphyxiation via immunohistochemistry, but total mRNA levels remain unchanged.
- SP-A is encoded by two distinct genes, SP-A1 and SP-A2, with differential gene expression.
Purpose of the Study:
- To establish a quantitative RT-PCR assay for SP-A1 and SP-A2 mRNA transcripts.
- To investigate the molecular pathology of SP-A in cases of acute mechanical asphyxia and drowning.
Main Methods:
- Developed a quantitative RT-PCR assay to measure SP-A1 and SP-A2 mRNA levels.
- Analyzed fatalities from acute mechanical asphyxia (n=12) and drowning (n=9).
- Compared findings with control groups: acute myocardial infarction (n=11) and brain lacerations (n=6).
Main Results:
- The SP-A1/A2 mRNA ratio was markedly elevated in mechanical asphyxia (mean 6.72) and drowning (mean 5.64).
- Control groups showed lower SP-A1/A2 ratios: acute myocardial infarction (mean 2.80) and brain lacerations (mean 2.56).
Conclusions:
- The SP-A1/A2 mRNA ratio is a potential biomarker for differentiating acute asphyxial deaths.
- Analysis of the SP-A1/A2 ratio can aid in interpreting molecular alterations of SP-A in asphyxial fatalities.
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