Sleep of two inbred rat strains

1969 ◽  
Author(s):  
W. B. Webb ◽  
J. K. Friedmann
2003 ◽  
Vol 196 (2) ◽  
pp. 135-141 ◽  
Author(s):  
Satoshi Ishizuka ◽  
Ayumu Takeuchi ◽  
Masahito Hagio ◽  
Mayuko Mohara ◽  
Hiroaki Sakai ◽  
...  

1965 ◽  
pp. 197-203 ◽  
Author(s):  
B. Frenzl ◽  
R. Brdička ◽  
V. Křen ◽  
O. Štark

1965 ◽  
pp. 197-203 ◽  
Author(s):  
B. Frenzl ◽  
R. Brdička ◽  
V. Křen ◽  
O. Štark

1993 ◽  
Vol 74 (2) ◽  
pp. 538-544 ◽  
Author(s):  
R. J. Dandurand ◽  
L. J. Xu ◽  
J. G. Martin ◽  
D. H. Eidelman

To investigate if airway-parenchymal interdependence may account for differing bronchial responsiveness between inbred rat strains, Fisher and Lewis 12-wk-old male rats were anesthetized, tracheostomized, and placed in a pressure plethysmograph. Functional residual capacity, total lung capacity [lung volume at transpulmonary pressure (PL) of 30 cmH2O], and specific compliance were determined and were found to be similar. Rats were paralyzed and mechanically ventilated. Concentration-response curves were constructed by calculating lung resistance (RL) and lung elastance (EL) after nebulization of saline and then doubling doses of methacholine (0.0625–512 mg/ml). In Fisher (n = 8) and Lewis (n = 7) rats RL and EL were again determined at a lung volume corresponding to 2 cmH2O PL above FRC. The doubling, maximal, and half-maximal effective concentrations were determined for RL and EL. The doubling of effective concentrations of RL and EL were significantly less for Fisher rats. Other groups of Fisher (n = 5) and Lewis (n = 5) rats were similarly exposed to three concentrations of methacholine (64, 128, and 256 mg/ml), and determinations of RL and EL were made at lung volume corresponding to PL of 0, 2, 4, and 8 cmH2O. In both groups, Lewis rats exhibited a significant effect of volume on maximal RL and EL, whereas Fisher rats did not. The absence of volume effect on bronchoconstriction in the hyperresponsive Fisher strain is consistent with the hypothesis that altered airway-parenchymal interdependence contributes to bronchial hyperresponsiveness.


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