Objective By establishing the rat model of positive acceleration adaptive training and observing the effects of adaptive training on gastric mucosal injury after positive acceleration in rats.The TXB2、6-Keto-PGF1a、PGE2、COX-1 mRNA and COX-2mRNA content in gastric mucosa were detected,and the TXB2/6-K-PGF1 a ratio were calculated.To assess the protective mechanism of positive acceleration adaptive training on gastric mucosa in rats and to provide theoretical basis for the prevention of gastric mucosal injury-related diseases for pilots and astronauts.Methods Forty male SD rats were randomly divided into five groups:A、B、C、D and E.Group A was the control group,and did not undergo any treatment.Group B was exposed to +5 Gz for 5 minutes per day over 5 consecutive days.Group C was exposed to +10 Gz for 5 minutes per day over 5 consecutive days.Group D was exposed to +4Gz for 3 minutes per day over 5 consecutive days and +5 Gz for 5minutes per day over another 5 consecutive days.Group E was exposed to +4 Gz for3 minutes per day over 5 consecutive days and +10 Gz for 5 minutes per day over another 5 consecutive days.The damage to the gastric mucosa was then observed grossly and under a microscope to calculate the damage index.The TXB2 、6-Keto-PGF1 a and PGE2 content in gastric mucosa was detected by ELISA,the TXB2/6-K-PGF1 a ratio were calculate,the COX-1 mRNA and COX-2 mRNA content were detected by PT-PCR.Results(1)On unaided visual and microscopic observations,all groups developed mucosa damage,with the exception of group A.The lesion index was significantly higher in group C than in group B(5.625±1.767 vs 1.750±0.707,P < 0.05).After adaptive training,the lesion index was significantly lower in group D than in group B(0.875±0.641 vs 1.750±0.707,P<0.05)and in group E than in group C(2.250±1.035 vs 5.625±1.767,P<0.05).(2)The content of TXB2 was significantly higher in group B than in group A(251.018pg/ml±50.845 pg/ml vs 121.400 pg/ml±41.629 pg/ml,P<0.05),and in group C than in group B(331.538 pg/ml±79.102 pg/ml vs 251.018 pg/ml±50.845 pg/ml,P<0.05).After adaptive training,the content of TXB2 was significantly lower in group D than in group B(159.588 pg/m L ± 36.216 pg/m L vs 251.018 pg/m L ± 50.845 pg/m L,P <0.01),and in group E than in group C(150.476 pg/m L ± 48.589 pg/m L vs 331.538pg/m L ± 79.102 pg/m L,P < 0.01).The content of 6-K-PGF1α was significantly lower in group B than in group A(52.015pg/ml±11.827 pg/ml vs 106.322 pg/ml±16.909 pg/ml,P<0.05),and in group C than in group A(44.726 pg/ml±18.867 pg/ml vs 106.322 pg/ml±16.909 pg/ml,P<0.05).After adaptive training,the content of 6-K-PGF1α was significantly higher in group D than in group B(72.242 pg/m L ±12.413 pg/m L vs 52.015 pg/m L ± 11.827 pg/m L,P <0.05),and in group E than in group C(87.426 pg/m L ± 15.833 pg/m L vs 44.726pg/m L ± 18.867 pg/m L,P < 0.05).The ratio of TXB2/6-K-PGF1α was significantly higher in group B than in group A(5.128±1.788 vs 1.199±0.545,P < 0.05),and in group C than in group B(8.599±4.157 vs 5.128±1.788,P < 0.05).After adaptive training,the ratio of TXB2/6-K-PGF1α was significantly lower in group D than in group B(2.283 ± 0.705 vs 5.128 ± 1.788,P < 0.01),and in group E than in group C(2.250 ± 1.035 vs 8.599 ±4.157,P < 0.01).(3)The content of PGE2 was significantly lower in group B than in group A(60.468pg/ml±9.697 pg/ml vs 81.462 pg/ml±20.340 pg/ml,P<0.05),and in group C than in group B(24.598 pg/ml±6.017 pg/ml vs 60.468 pg/ml±9.697 pg/ml,P<0.05).After adaptive training,the content of PGE2 was significantly higher in group E than in group C(46.165 pg/ml±13.996 pg/ml vs 24.598 pg/ml±6.017 pg/ml,P<0.05).(4)There was no significant differences on the expression of COX-1 mRNA in all groups(P>0.05).The expression of COX-2 mRNA was significantly higher in group B than in group A(1.492±0.281 vs 0.978±0.109,P<0.05),and in group C than group B and group A(2.642±0.320 vs 0.978±0.109,P<0.05;2.642±0.320 vs 1.492±0.281,P<0.05).After adaptive training,the expression of COX-2 mRNA was significantly higher in group D than in group B and in group E than group C(1.782±0.099 vs1.492±0.281,P<0.05;3.268±0.083 vs 2.642±0.320,P<0.05).(5)The content of 6-Keto-PGF1α and the expression of COX-1 mRNA,and the expression of COX-2 mRNA,had no significant correlation(P<0.05).The content of PGE2 and the expression of COX-1 mRNA,and the expression of COX-2 mRNA,had no significant correlation(P<0.05).Conclusion Adaptive training can significantly reduce the gastric mucosal damage caused by high +Gz value,and its mechanism is related to the increase in PGI2、PGE2content,and the reduce in TXA2 content、 TXA2/PGI2 ratio,and expression increase of COX-2 mRNA. |