G Schelling — Page 3 | PubMed Health

PubMedDate not supplied

Breakpoint distribution in male-linked translocations in Anopheles stephensi Liston.

A series of translocations involving the male chromosome and chromosome 3 was analyzed in Anopheles stephensi. Using three genetic markers in 3R, namely sp, dp, and Bl, the recombination distance between the breakpoint and each of the three markers was assessed. On the basis of control recombination it was possible to assign the breakpoint to the chromosome relative to the three markers. It was shown that the majority of breakpoints were located in the vicinity of dp-Bl and translocations were identified that showed complete linkage with each of the markers. The results are compared with the published data on radiation-induced breakage and used to interpret the difficulties that have been experienced in producing a genetic sexing system in this species.

Animals↗

PubMedDate not supplied

Improvement of lung preservation -- from experiment to clinical practice.

BACKGROUND: Reperfusion injury represents a severe early complication following lung transplantation. Among the pathogenetic factors, the high potassium content of Euro-Collins(reg) solution is discussed. MATERIAL AND METHODS: In a pig model of orthotopic left-sided lung transplantation we investigated the effect of Euro-Collins solution (EC: n = 6) versus low potassium dextran (LPD: Perfadex: n = 6). Sham-operated (n = 6) animals served as control. Transplant function, cellular energy metabolism and endothelial morphology served as parameters. In a clinical investigation, 124 patients were evaluated following single (EC: n = 31; LPD n = 37) or double (EC: n = 17; LPD n = 39) lung transplantation, whose organs where preserved with EC (n = 48) or LPD (n = 76). Duration of ischemia, duration of ventilation and stay on ICU were registered. Primary transplant function was evaluated according to AaDO(2) values. Cause of early death (30 days) was declared. RESULTS: Experimental results: After flush with EC and 18 h ischemia, a reduction of tissue ATP content (p < 0.01 vs inital value and LPD) was noted. Endothelial damage after ischemia was severe (p < 0.05 vs control), paO(2) was significantly decreased. CLINICAL RESULTS: In the LPD group, duration of ischemia was longer for the grafts transplanted first (SLTx and DLTx: p = 0.0009) as well as second (2. organ DLTx: p = 0.045). Primary transplant function was improved (day 0: SLTx: p = 0.0015; DLTx: p = 0.0095, both vs EC). Duration of ventilation and stay on ICU were shorter (n.s.). Reperfusion injury-associated death was reduced from 8% (EC) to 0 (LPD). CONCLUSION: In experimental lung preservation, LPD lead to an improved graft function. These results were confirmed in clinical lung transplantation. Clinical lung preservation, therefore, should be carried out by use of LPD.

Adult↗