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The response of the villus and crypt cells of the mouse jejunum to secretagogues has been assessed through measurements of cellular composition with x-ray microanalysis. In nonstimulated tissues the Na concentration ([Na]c) of the crypt cells was significantly less, and the K ([K]c) and Cl ([Cl]c) concentrations were significantly greater, than that of the villus cells. There was also a decreasing gradient of [Na]c and increasing gradient of [K]c from the villus tip to crypt base due to a greater number of cells with a high [Na]c and low [K]c in the upper regions of the villi. Theophylline (10 mmol L-1) stimulated a sustained increase in bumetanide sensitive short circuit current (Isc) and significantly decreased the [Na]c of the villus cells. Similar, but smaller changes were seen in the crypt cells. Changes in villus cell [Na]c reflected a reduction in the number of cells with a high [Na]c. Inhibition of the apical Na/H exchanger (1 mmol L-1 amiloride) had little effect on basal Isc and the subsequent addition of theophylline increased Isc to a comparable extent as seen without amiloride. However, after amiloride treatment the only change in cellular composition was a reduction in the [Cl]c of both crypt and villus cells, suggesting that both regions are involved in the secretory response. These data suggest that the dominant response of the jejunum to secretagogues is an inhibition of Na absorption via Na/H exchange in the villi and the secretory response is distributed throughout the crypt/villus axis.

Growth and photosynthesis of Agrostis capillaris L. and Nardus stricta L. were measured for plants grown under ambient and elevated concentrations of CO2 (340 and 550 μl CO2 l(-1) respectively) and a range of nitrogen concentrations (0.01, 0.1, 1 and 5 mg N l(-1) ) supplied as either ammonium sulphate or sodium nitrate. After 42 d of growth for A. capillaris and 49 d of growth for N. stricta, the higher nitrogen concentrations resulted in stimulation of growth. The form of nitrogen did not affect the total dry weight attained by A. capillaris. However, ammonium-grown N. stricta attained a greater total dry weight than did nitrate-grown plants. Nitrogen form influenced leaf area ratio, which was greater in nitrate-grown A. capillaris and in ammonium-grown N. stricta. At the two lowest nitrogen concentrations there was no effect of elevated CO2 on total dry weight in either species, whilst at the two highest nitrogen concentrations positive growth responses to elevated C02 were observed. Photosynthetic capacity and carboxylation efficiency were lower in plants grown in elevated CO2 at the two lowest nitrogen concentrations, and were associated with greater leaf soluble carbohydrate content and lower foliar nitrogen concentrations. By contrast, the CO2 treatment did not affect these parameters at the two highest nitrogen concentrations employed.

Rabbit iris-ciliary bodies were preincubated in control and experimental Ringer's solutions before quick freezing, cryosectioning, dehydration and electron probe X-ray microanalysis. After preincubation in a baseline bicarbonate-free Cl- Ringer's solution, the ciliary epithelial intracellular Na+, K+ and Cl- concentrations were estimated to be 15 +/- 3, 162 +/- 14 and 46 +/- 5 mmol kg-1 intracellular water, respectively. The water and elemental Na, K, Cl and P contents were similar in the non-pigmented (NPE) and pigmented (PE) ciliary epithelial cells. As expected, inhibition of the Na,K-exchange pump by preincubation with ouabain markedly increased the intracellular Na content, and markedly reduced the intracellular K content, verifying the validity of the experimental analysis. The Cl- channels of the NPE cells likely play a critical role in determining the rate of aqueous humor formation. Therefore, we have examined the effects of altering Cl- transport on the intracellular composition in this initial microprobe study of the ciliary epithelium. As expected, exposure to bicarbonate increased the intracellular Cl and water contents. Replacement of external Cl- by NO3- was twice as effective as replacement by gluconate in leaching Cl- out of the intracellular compartment. An unexpected finding was that NO3- replacement of internal Cl- substantially increased the intracellular Na and decreased the intracellular K content, possibly by stabilizing the Na,K-pump in the E1P form and inhibiting enzyme activity.