Objectives:Death fear is the main subject in thanatology.Several researchers have defined different reasons for fear of death.This study aimed to explore the performance of the Farsi version of the Reasons for Death F...Objectives:Death fear is the main subject in thanatology.Several researchers have defined different reasons for fear of death.This study aimed to explore the performance of the Farsi version of the Reasons for Death Fear Scale(RDFS)among a convenience sample of Iranian nurses(n=106).Methods:The nurses were selected by the convenience sampling method and were asked to complete the RDFS,Death Concern Scale,Collett-Lester Fear of Death Scale,Death Anxiety Scale,Death Depression Scale,and Death Obsession Scale.Results:For the RDFS,the Cronbach's a coefficient was 0.90,and the 2-week test-retest reliability was 0.64.The RDFS was correlated at 0.34,0.39,0.50,0.35,and 0.39 to the above-mentioned five scales,indicating its good construct and criterion-related validity.Based on the exploratory factor analysis,the RDFS-identified four factors accounted for 66.20%of the variance and were labeled as"Fear of Pain and Punishment,""Fear of Losing Worldly Involvements,""Religious Transgressions and Failures,"and"Parting from Loved Ones."Conclusions:The RDFS presents good validity and reliability and can be used in clinical and research settings in Iran.展开更多
As a potent pleiotropic cytokine, tumor necrosis factor-alpha （TNF-ct） plays an important role in innate immune responses. The cDNA sequence and genomic structure of the TNF-α gene （AjTNF-c0 in the Japanese eel （...As a potent pleiotropic cytokine, tumor necrosis factor-alpha （TNF-ct） plays an important role in innate immune responses. The cDNA sequence and genomic structure of the TNF-α gene （AjTNF-c0 in the Japanese eel （Anguilla japonica） were identified and characterized. The full-length AjTNF-α cDNA was 1 546 bp, including a 5＇-untranslated region （UTR） of 13 bp, a 3＇-UTR of 879 bp and an open reading frame of 654 bp encoding a protein of 218 amino acids. The full-length genomic sequence of AjTNF-ct was 2 392 bp and included four exons and three introns. The putative AjTNF-α protein contained TNF family signature motifs, including a protease cleavage site, a transmembrane domain and two conserved cysteine residues. Quantitative real-time reverse transcription PCR analysis revealed AjTNF-α expression in a wide range of tissues, with predominant expression in blood and liver. Lower levels of expression were seen in spleen, gills, kidney, intestine, heart, and skin, with very low levels in muscle. The modulation of AjTNF-ct expression after injection of eels with lipopolysaccharide （LPS）, the viral mimic, poly I：C, or Aeromonas hydrophila was assessed in blood, liver, and kidney. In blood, TNF-α mRNA levels increased rapidly and then rapidly decreased after stimulation with LPS, poly I：C or A. hydrophila. However, the response to LPS and A. hydrophila peaked at 6 h while for poly I：C the peak was at 12 h. In liver, after injection with A. hydrophila, an up- and down-regulation of AjTNF-ct expression occurred twice, peaking at 6 h and 24 h, respectively. No remarkable increase of AjTNF-α expression appeared in liver until 72 h after LPS or poly I：C treatment. In kidney, ApiNF-α expression increased significantly only at 72 h post-stimulation with LPS orA. hydrophila. Our results suggest that AjTNF-α plays an important role in fish in the defense against viral and bacterial infection.展开更多
AIM:To assess the hepatic changes after induction of different periods of renal ischemia. METHODS:Rats were subjected to either sham operation or ischemia (30,45 and 60 min) followed by 60 min reperfusion. Liver and r...AIM:To assess the hepatic changes after induction of different periods of renal ischemia. METHODS:Rats were subjected to either sham operation or ischemia (30,45 and 60 min) followed by 60 min reperfusion. Liver and renal functional indices were measured. Hepatic glutathione (GSH) and ferric reducing antioxidant power levels and the concentration of interleukin (IL)-10 and tumor necrosis factor (TNF-α) were evaluated. Portions of liver and kidney tissues were fixed for histological evaluation. RESULTS:Forty-five minutes renal ischemia followed by 60 min reperfusion caused significant changes in liver structure and a significant reduction in renalfunction. These rats showed a significant decrease in liver GSH,as well as a significant increase in TNF-α and IL-10 concentrations. These results demonstrated that renal ischemia caused changes in liver histology,function,oxidative stress and inflammatory status,which led to a reduction in hepatic antioxidant capacity. With 30 min ischemia,the magnitude of these changes was less than those with 45 or 60 min ischemia.CONCLUSION:A minimum of 45 min ischemia is needed to study the effects of renal injury on the liver as a remote organ.展开更多
文摘Objectives:Death fear is the main subject in thanatology.Several researchers have defined different reasons for fear of death.This study aimed to explore the performance of the Farsi version of the Reasons for Death Fear Scale(RDFS)among a convenience sample of Iranian nurses(n=106).Methods:The nurses were selected by the convenience sampling method and were asked to complete the RDFS,Death Concern Scale,Collett-Lester Fear of Death Scale,Death Anxiety Scale,Death Depression Scale,and Death Obsession Scale.Results:For the RDFS,the Cronbach's a coefficient was 0.90,and the 2-week test-retest reliability was 0.64.The RDFS was correlated at 0.34,0.39,0.50,0.35,and 0.39 to the above-mentioned five scales,indicating its good construct and criterion-related validity.Based on the exploratory factor analysis,the RDFS-identified four factors accounted for 66.20%of the variance and were labeled as"Fear of Pain and Punishment,""Fear of Losing Worldly Involvements,""Religious Transgressions and Failures,"and"Parting from Loved Ones."Conclusions:The RDFS presents good validity and reliability and can be used in clinical and research settings in Iran.
基金Supported by the Ocean and Fishery Bureau of Fujian Province(No.201212140006)the Scientific Research Foundation of Jimei University,China(No.ZQ2008013)+1 种基金the National Natural Science Foundation of China(No.31272685)the Program of the Education Department of Fujian Province(No.JA11150)
文摘As a potent pleiotropic cytokine, tumor necrosis factor-alpha （TNF-ct） plays an important role in innate immune responses. The cDNA sequence and genomic structure of the TNF-α gene （AjTNF-c0 in the Japanese eel （Anguilla japonica） were identified and characterized. The full-length AjTNF-α cDNA was 1 546 bp, including a 5＇-untranslated region （UTR） of 13 bp, a 3＇-UTR of 879 bp and an open reading frame of 654 bp encoding a protein of 218 amino acids. The full-length genomic sequence of AjTNF-ct was 2 392 bp and included four exons and three introns. The putative AjTNF-α protein contained TNF family signature motifs, including a protease cleavage site, a transmembrane domain and two conserved cysteine residues. Quantitative real-time reverse transcription PCR analysis revealed AjTNF-α expression in a wide range of tissues, with predominant expression in blood and liver. Lower levels of expression were seen in spleen, gills, kidney, intestine, heart, and skin, with very low levels in muscle. The modulation of AjTNF-ct expression after injection of eels with lipopolysaccharide （LPS）, the viral mimic, poly I：C, or Aeromonas hydrophila was assessed in blood, liver, and kidney. In blood, TNF-α mRNA levels increased rapidly and then rapidly decreased after stimulation with LPS, poly I：C or A. hydrophila. However, the response to LPS and A. hydrophila peaked at 6 h while for poly I：C the peak was at 12 h. In liver, after injection with A. hydrophila, an up- and down-regulation of AjTNF-ct expression occurred twice, peaking at 6 h and 24 h, respectively. No remarkable increase of AjTNF-α expression appeared in liver until 72 h after LPS or poly I：C treatment. In kidney, ApiNF-α expression increased significantly only at 72 h post-stimulation with LPS orA. hydrophila. Our results suggest that AjTNF-α plays an important role in fish in the defense against viral and bacterial infection.
基金Supported by A grant from Tehran Medical Sciences University
文摘AIM:To assess the hepatic changes after induction of different periods of renal ischemia. METHODS:Rats were subjected to either sham operation or ischemia (30,45 and 60 min) followed by 60 min reperfusion. Liver and renal functional indices were measured. Hepatic glutathione (GSH) and ferric reducing antioxidant power levels and the concentration of interleukin (IL)-10 and tumor necrosis factor (TNF-α) were evaluated. Portions of liver and kidney tissues were fixed for histological evaluation. RESULTS:Forty-five minutes renal ischemia followed by 60 min reperfusion caused significant changes in liver structure and a significant reduction in renalfunction. These rats showed a significant decrease in liver GSH,as well as a significant increase in TNF-α and IL-10 concentrations. These results demonstrated that renal ischemia caused changes in liver histology,function,oxidative stress and inflammatory status,which led to a reduction in hepatic antioxidant capacity. With 30 min ischemia,the magnitude of these changes was less than those with 45 or 60 min ischemia.CONCLUSION:A minimum of 45 min ischemia is needed to study the effects of renal injury on the liver as a remote organ.
