Active Transport by the Cecropia Midgut

1968 ◽  
Vol 48 (1) ◽  
pp. 25-37
Author(s):  
J. A. HASKELL ◽  
W. R. HARVEY ◽  
R. M. CLARK

1. The electrical potential across the isolated midgut of five developmental stages of the Cecropia silkworm was studied by changing the concentration of single cations in solutions bathing each side of the midgut. The stages included feeding fourth-instar insects, insects moulting from the fourth to the fifth instar, feeding fifth-instar insects, insects which had evacuated their midguts, and insects spinning cocoons. 2. Average values of the initial maximal potential exhibited by the midgut in solutions containing K, Mg, and Ca but no Na, for the stages mentioned above, were 68, 83, 90, 124, and 2 mV., respectively. 3. In all of the developmental stages studied except the ‘spinning larva’, reducing the potassium concentration from 32 to 2 mM/l. on the blood-side of the isolated gut lowers the potential, on the lumen-side of the gut raises the potential and on both sides gives an intermediate value. 4. When the potential prior to a decrease in concentration of potassium on the blood-side is over 100 mV., the Nernst slope approaches 59 mV. 5. A tenfold reduction in the concentration of magnesium or the addition of 32 mM/l. sodium to the solutions bathing the isolated gut has no systematic effect on the potential. 6. A tenfold drop in the concentration of calcium in the solutions causes changes in the potential in the opposite direction from those predicted by the Nernst equation. 7. The pH of the midgut contents rises from early fourth instar to late fifth instar. The hydrogen-ion concentration of the blood is about 1000 times more than that of midgut contents in fifth-instar insects. 8. Neither synthetic ecdysone, partially purified natural ecdysone nor juvenile hormone has an effect on the potential or current of the isolated midgut over periods as long as 30 min.

1934 ◽  
Vol 17 (5) ◽  
pp. 629-656 ◽  
Author(s):  
Wallace O. Fenn ◽  
Doris M. Cobb

1. Analyses were made of the K and HCO3 content, the irritability, and weight change of isolated frog sartorius muscles after immersion for 5 hours in Ringer's solutions modified as to pH and potassium content. 2. At each pH a concentration of potassium in the solution was found which was in diffusion equilibrium with the potassium in the muscle. In greater concentrations potassium moved into the muscle against the concentration gradient and vice versa. 3. The greater the alkalinity of the solution the smaller the concentration of the potassium at equilibrium so that the product of the concentrations of OH and K in the solution at equilibrium tends to remain approximately constant. 4. The pH inside the muscle is approximately equal to that outside when first dissected but it tends to change during immersion so as to follow the changes in the pH of the solution. This finding is in direct conflict with the theory according to which the high potassium concentration inside should be accompanied by an equally high hydrogen ion concentration in relation to that outside. 5. The diffusion of potassium into the muscle makes its contents more alkaline but the increase in alkalinity is not always, nor usually, equivalent to the amount of potassium which has diffused and conversely, the pH inside can change in either direction according to the pH outside without there being any diffusion of potassium. Hence potassium is not the only penetrating ion. 6. The irritability of the muscles is at a maximum in concentrations of potassium which are greater than that in normal Ringer's solution, or about 20 mg. per cent potassium. This optimum does not seem to be a function of pH and is therefore not dependent upon the direction of movement of the potassium but probably on the ratio of potassium outside to that inside. 7. Swelling of the muscles occurs in solutions which injure the muscle so as to permit both cations and anions to enter without permitting the organic protein anions to escape. Anion impermeability is necessary to prevent this same osmotic swelling under normal conditions. 8. An increase in the CO2 tension in muscle and solution causes a greater increase in acidity in the solution than in the muscle and leads to a loss of potassium. One expects therefore a potassium shift from tissues to blood comparable to the chlorine shift from plasma to corpuscles.


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