Laboratory incubation experiment was conducted to study the effect of lime nitrogen(LN) on transfor-mation of iirea-N in three paddy soils. The results showed that LN had an inhibitory effect on urease activityin thes...Laboratory incubation experiment was conducted to study the effect of lime nitrogen(LN) on transfor-mation of iirea-N in three paddy soils. The results showed that LN had an inhibitory effect on urease activityin these soils especially in the first 5 days, and that in the first 20 days of incubation, the amount of NH-Nderived from urea was lower in the soil with LN than in the soil without LN. While after 30 days the ainountof NH-N was higher in the mature haplic paddy soil developed on Quaternary red clay(MHPS) with LNthan that in the soil without LN. The amonnt of NH_3-N volatilized was decreased in the earlier stage andincreased in the later stage of incubation in the MHPS by the addition of LN.展开更多
Objective To investigate the relationship between expression of somatostatin receptors(SSTRs) and activation of rat hepatic stellate cell (HSC). Methods HSCs were isolated from rats by in situ perfusion and single-ste...Objective To investigate the relationship between expression of somatostatin receptors(SSTRs) and activation of rat hepatic stellate cell (HSC). Methods HSCs were isolated from rats by in situ perfusion and single-step density gradient centrifugation, and then SSTR1-5 mRNA levels in the differentiated first passage HSCs were detected by means of reverse transcription polymerase chain reaction. On the other hand, hepatic fibrosis was induced in adult male Sprague-Dawley rats by carbon tetrachloride intoxication, and the expression of SSTR1-5 in normal as well as fibrotic liver was measured by immunohistochemical staining. Results SSTR mR-NA and SSTR could not be found in freshly isolated rat HSCs and normal rat liver. But SSTR1-3 mRNA appeared as HSCs became wholly activated, and SSTR1-3 could also be identified on the membrane of activated HSCs in the peri-sinusoid space, fibrous septa, etc. Conclusion The expression of SSTR1-3 in the rat HSC is closely related to its activation. This may reflect one of the main negative regulation mechanisms in the course of HSC activation.展开更多
文摘Laboratory incubation experiment was conducted to study the effect of lime nitrogen(LN) on transfor-mation of iirea-N in three paddy soils. The results showed that LN had an inhibitory effect on urease activityin these soils especially in the first 5 days, and that in the first 20 days of incubation, the amount of NH-Nderived from urea was lower in the soil with LN than in the soil without LN. While after 30 days the ainountof NH-N was higher in the mature haplic paddy soil developed on Quaternary red clay(MHPS) with LNthan that in the soil without LN. The amonnt of NH_3-N volatilized was decreased in the earlier stage andincreased in the later stage of incubation in the MHPS by the addition of LN.
基金Supported by the Scientific Development Programs of Science and Technology Commission Foundation of Shanghai (004119047).
文摘Objective To investigate the relationship between expression of somatostatin receptors(SSTRs) and activation of rat hepatic stellate cell (HSC). Methods HSCs were isolated from rats by in situ perfusion and single-step density gradient centrifugation, and then SSTR1-5 mRNA levels in the differentiated first passage HSCs were detected by means of reverse transcription polymerase chain reaction. On the other hand, hepatic fibrosis was induced in adult male Sprague-Dawley rats by carbon tetrachloride intoxication, and the expression of SSTR1-5 in normal as well as fibrotic liver was measured by immunohistochemical staining. Results SSTR mR-NA and SSTR could not be found in freshly isolated rat HSCs and normal rat liver. But SSTR1-3 mRNA appeared as HSCs became wholly activated, and SSTR1-3 could also be identified on the membrane of activated HSCs in the peri-sinusoid space, fibrous septa, etc. Conclusion The expression of SSTR1-3 in the rat HSC is closely related to its activation. This may reflect one of the main negative regulation mechanisms in the course of HSC activation.
