scholarly journals RELATION OF METABOLISM OF FROG SKIN TO CELLULAR INTEGRITY AND ELECTROLYTE TRANSFER

1953 ◽  
Vol 36 (5) ◽  
pp. 607-615 ◽  
Author(s):  
Norman G. Levinsky ◽  
Wilbur H. Sawyer

1. The transport of sodium by frog skin and the maintenance of normal potassium levels within the cells of the skin are both dependent on metabolism and on a supply of phosphate bond energy. 2. Except for the common requirement of phosphate bond energy, the transfer mechanism for sodium and the mechanism for maintaining intracellular potassium appear to be independent. 3. The xanthines specifically inhibit the sodium transfer mechanism; at higher concentrations, they depress metabolism and cause loss of potassium from the skin.

Nature ◽  
1953 ◽  
Vol 171 (4365) ◽  
pp. 1147-1149 ◽  
Author(s):  
R. J. GILLESPIE ◽  
G. A. MAW ◽  
C. A. VERNON
Keyword(s):  

2020 ◽  
pp. 281-296
Author(s):  
Hans-Martin Gärtner ◽  
Jens Michaelis

This chapter revisits previous work (Gärtner and Michaelis 2010), which discusses the prospects of theories that derive the distribution of V2-declaratives from their affinity with assertive illocutionary force (potential). It reiterates the challenge disjunctive coordination of V2-declaratives poses to commitment-based contruals of assertion. Likewise, it restates the take on this challenge in earlier work which ‘weakens assertion’ to proposition-level intersection with the common ground. Against the backdrop of this proposal, two recent approaches to the ‘disjunction challenge’ are analysed: (i) a feature-transfer mechanism proposed by Julien (2015), which exempts V2-disjuncts from being directly asserted; (ii) a discourse model developed by Antomo (2016), which discards assertion and, instead, requires the content of V2-declaratives to be relevant to the current question(s) under discussion. The chapter shows that both these approaches run up against serious obstacles, compositionality in the former case, the hard to control flexibility of question-answer relations in context in the latter (among other things). It goes on to conclude that the ‘disjunction challenge’ to accounts of the distribution of V2-declaratives still stands.


1957 ◽  
Vol 35 (1) ◽  
pp. 835-843 ◽  
Author(s):  
D. P. Burma ◽  
D. C. Mortimer

Disks of sugar beet leaf that had assimilated C14O2 in light for 10 to 30 seconds were exposed to C12O2 in light or darkness, or in combinations of both for periods of 4 to 25 minutes. The changes in distribution of C14 among the compounds soluble in 80% ethanol were examined as a function of time for each "flush" treatment. In light, most of the C14 ultimately accumulates in sucrose, while phosphoglycerate, phosphoenolpyruvate, sugar phosphates, glycine, and serine have more transitory roles. In dark, sucrose is formed much more slowly than in light while alanine becomes the main repository of C14. In light following darkness, the accumulation of C14 in alanine is reversed in favor of its accumulation in sucrose, with the sugar phosphates acting as intermediates. In dark following light, the converse does not occur; sugar phosphates and alanine lose, rather than gain, C14, and sucrose shows little tendency to be metabolized. It is suggested that one of the factors directing the course of these interconversions is the level of light-produced phosphate bond energy needed for sucrose synthesis.


1957 ◽  
Vol 35 (10) ◽  
pp. 835-843 ◽  
Author(s):  
D. P. Burma ◽  
D. C. Mortimer

Disks of sugar beet leaf that had assimilated C14O2 in light for 10 to 30 seconds were exposed to C12O2 in light or darkness, or in combinations of both for periods of 4 to 25 minutes. The changes in distribution of C14 among the compounds soluble in 80% ethanol were examined as a function of time for each "flush" treatment. In light, most of the C14 ultimately accumulates in sucrose, while phosphoglycerate, phosphoenolpyruvate, sugar phosphates, glycine, and serine have more transitory roles. In dark, sucrose is formed much more slowly than in light while alanine becomes the main repository of C14. In light following darkness, the accumulation of C14 in alanine is reversed in favor of its accumulation in sucrose, with the sugar phosphates acting as intermediates. In dark following light, the converse does not occur; sugar phosphates and alanine lose, rather than gain, C14, and sucrose shows little tendency to be metabolized. It is suggested that one of the factors directing the course of these interconversions is the level of light-produced phosphate bond energy needed for sucrose synthesis.


1955 ◽  
Vol 38 (6) ◽  
pp. 867-888 ◽  
Author(s):  
Ernst G. Huf ◽  
Joyce P. Wills ◽  
Mary F. Arrighi

1. The "chloride space" in frog skin was determined and found to be 69.7 per cent by weight of wet skin. The chloride space occupies about 94 per cent of the total water space of skin. From this and other information, it appears that the "non-chloride space" measures only a part of the space occupied by the structural elements of skin. This space is referred to here as the intracellular compartment and the remainder as the extracellular compartment of frog skin. On this basis, potassium and sodium in skin are distributed as follows: total sodium, 60 to 75 µeq./gm. of wet skin; all sodium is probably extracellular; total potassium, 39 to 49 µeq./gm.; intracellular potassium, 37 to 47 µeq./gm. 2. Skins were immersed in solutions differing from each other in their sodium and potassium concentrations. Three levels of NaCl were studied: 48, 119, and 169 µeq./ml. For each of these solutions (referred to below as diluted, physiological, and concentrated saline), the potassium levels were varied from 0.1 to 20 µeq./ml. For skins in solutions low in potassium and high in sodium, it was found that an exchange of intracellular potassium against extracellular sodium occurs. The ratio for the number of potassium ions lost/number of sodium ions gained was 4:1,4:6, and 4:8 for skin in K+-free diluted, physiological, and concentrated saline, respectively. 3. Uptake of NaCl by the epithelium of frog skin is dependent on the potassium concentration of the environment. For skins in physiological saline, net uptake of NaCl was optimal (0.90 µeq. x cm.–2 x hr.–1) at 1 to 5 µeq. K+/ml. For skins in diluted and concentrated saline optimal NaCl uptake was seen at potassium concentrations of approximately 5 and 10 µeq. K+/ml., respectively. Net uptake of NaCl by the skin is also discussed, with relation to the potassium balance of skin. 4. Skin potentials decreased with increasing extracellular potassium concentration when diluted saline solutions were used. The opposite of this was found for skins in concentrated saline. For skins in physiological saline, skin potentials rose sharply from rather low values, when placed in solutions very low in potassium, to relatively high values, when immersed in solutions containing 1 to 5 µeq. K+/ml. Further increase in potassium concentration of the bath led to slight reductions in skin potentials. The highest potentials observed were of the order of 40 mv. In all cases studied, the inside was positive with relation to the outside. 5. It can be shown that values for intracellular potassium concentration as a function of extracellular potassium concentration satisfy, at a first but good approximation, Freundlich's isotherm. A modification of Freundlich's isotherm, recently introduced by Sips, may also be used to correlate the experimental data quantitatively. Since the latter isotherm has a rational interpretation, it is suggested that this be used, rather than Freundlich's isotherm, to express quantitatively the dependence of intracellular on extracellular potassium in frog skin.


1974 ◽  
Vol 47 (1) ◽  
pp. 89-92
Author(s):  
J. N. Norman ◽  
J. R. Shearer ◽  
G. Smith

1. The effect of high oxygen pressures on sodium transport across the isolated frog skin was investigated. 2. No effect on sodium transport was found when the skin was exposed to oxygen at 2 atmospheres pressure for 1 h.


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