scholarly journals Effect of hurdling step strategy on the kinematics of the hurdle clearance technique

2021 ◽  
pp. 1-15
Author(s):  
Lee J. Rowley ◽  
Sarah M. Churchill ◽  
Marcus Dunn ◽  
Jon Wheat
Keyword(s):  
1997 ◽  
Vol 99 (2) ◽  
pp. 493-505 ◽  
Author(s):  
Hans-Guenther Machens ◽  
Peter Mailaender ◽  
Ralf Reimer ◽  
Norbert Pallua ◽  
Yuan Lei ◽  
...  

2017 ◽  
Vol 16 ◽  
pp. S132
Author(s):  
K.A. Lavery ◽  
D. O'Gorman ◽  
C. Devine ◽  
L. Carson ◽  
J. Rendall

1986 ◽  
Vol 6 (3) ◽  
pp. 338-341 ◽  
Author(s):  
Nicholas V. Todd ◽  
Piero Picozzi ◽  
H. Alan Crockard

CBF obtained by the hydrogen clearance technique and cerebral blood volume (CBV) calculated from the [14C]dextran space were measured in three groups of rats subjected to temporary four-vessel occlusion to produce 15 min of ischaemia, followed by 60 min of reperfusion. In the control animals, mean CBF was 93 ± 6 ml 100 g−1 min−1, which fell to 5.5 ± 0.5 ml 100 g−1 min−1 during ischaemia. There was a marked early postischaemic hyperaemia (262 ± 18 ml 100g−1 min−1), but 1 h after the onset of ischaemia, there was a significant hypoperfusion (51 ± 3 ml 100 g−1 min−1). Mean cortical dextran space was 1.58 ± 0.09 ml 100 g−1 prior to ischaemia. Early in reperfusion there was a significant increase in CBV (1.85 ± 0.24 ml 100 g−1) with a decrease during the period of hypoperfusion (1.33 ± 0.03 ml 100 g−1). Therefore, following a period of temporary ischaemia, there are commensurate changes in CBF and CBV, and alterations in the permeability–surface area product at this time may be due to variations in surface area and not necessarily permeability.


1963 ◽  
Vol 205 (3) ◽  
pp. 489-493 ◽  
Author(s):  
Agamemnon Despopoulos ◽  
Lloyd H. Pendergrass ◽  
John M. Stoeckinger

Analogues of phenylbutazone were tested for inhibitory potency in the renal transport mechanism for 4-aminohippurate. In a series of ten compounds examined by an in vitro technique, no correlation could be demonstrated between inhibitory potency and acidic strength of the inhibitor either in rabbit or in dog tissues. In a further series of 16 paired analogues, the hydroxylated member of each pair was 3–4 times less potent than its unhydroxylated counterpart. Correlations between molecular structure and pharmacological activity are suggested. In contrast to these observations, each of three selected phenylbutazone analogues (phenylbutazone, metabolite II, and sulfinpyrazone) depressed the maximum tubular excretory rate for 4-aminohippurate in intact dogs, but apparent inhibitory potencies by the clearance technique were unrelated to inhibitory potencies in dog kidney slices. Differences in relative potencies thus obtained are attributed to differences in metabolic alteration of each compound at extrarenal sites in intact dogs.


1974 ◽  
Vol 348 (1) ◽  
pp. 51-57 ◽  
Author(s):  
Meral T. Ercan ◽  
Naci M. Bor ◽  
Co?kun F. Bekdik ◽  
G�lsen �ner

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