A Comparison of the Effects of Metabolic Inhibitors on Chloride Uptake and Photosynthesis In Chara Oorallina

A comparative study has been made of the effects of four metabolic inhibitors on chloride uptake and photosynthetic 14C02 fixation by cells of O. corallina, and on oxygen evolution by chloropl<1sts isolated from the cells. Low concentrations of phlorizin and Dio-9 inhibited chloride uptake, but this was not accompanied by an inhibition of photosynthesis in vivo, and could not be correlated with the measured inhibition of electron flow in vitro. Low concentrations of imidazole stimulated the chloride influx in light, but there was again no effect on photosynthetic 14C02 fixation, although imidazole did uncouple electron flow in vitro. The effect of imidazole was dependent on the pH of the external solution. Increasing concentrations of carbonyl cyanide m-chlorophenylhydrazone progressively reduced the chloride influx and 14C02 fixation, and uncoupled electron flow in vitro. The work provides no evidence to support the view that chloride uptake is directly linked to electron flow rather than phosphorylation.

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Steroid effects on permeability of rat thymic lymphocytes to α-aminoisobutyrate

American Journal of Physiology-Legacy Content ◽

10.1152/ajplegacy.1963.205.3.446 ◽

1963 ◽

Vol 205 (3) ◽

pp. 446-452 ◽

Cited By ~ 2

Author(s):

Melvin Blecher

Keyword(s):

Skeletal Muscle ◽

Extracellular Fluid ◽

In Vivo Studies ◽

Metabolic Inhibitors ◽

Active Process ◽

Low Concentrations ◽

Significant Difference ◽

Adrenalectomized Rats

In vitro studies of the flux of α-aminoisobutyrate-1-C14 (AIB) between rat thymic lymphocytes and extracellular fluid have revealed that: a) the amino acid enters cells but is not further metabolized; b) at low concentrations, similar to those of amino acids in plasma, the net influx and efflux of AIB exhibit properties of an active process; and c) influx of AIB is inhibited, and efflux stimulated, by deoxycorticosterone (DOC), by metabolic inhibitors, and by other specific steroids. In vivo studies of the distribution of AIB between serum and tissue demonstrated that administration of DOC to adrenalectomized rats inhibited concentration of AIB by thymus, diaphragm, and skeletal muscle, augmented uptake by liver, and increased the serum level of AIB. Prior adrenalectomy of donor rats resulted in no change from normal in the in vitro capacity of thymic lymphocytes to take up AIB. There was no significant difference from normal in the in vivo concentration of AIB by thymus, liver, and skeletal muscle of adrenalectomized rats, although uptake by diaphragm was decreased compared to normal control animals.

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Absorption of pantothenic acid in rat and chick intestine

AJP Gastrointestinal and Liver Physiology ◽

10.1152/ajpgi.1986.250.2.g155 ◽

1986 ◽

Vol 250 (2) ◽

pp. G155-G160

Author(s):

D. K. Fenstermacher ◽

R. C. Rose

Keyword(s):

Pantothenic Acid ◽

Potential Gradient ◽

Metabolic Inhibitors ◽

Transepithelial Transport ◽

Simple Diffusion ◽

Low Concentrations ◽

Saturation Kinetics ◽

Sodium Dependent

Pantothenic acid absorption was evaluated in the intestine of rat and chicken to reevaluate the concept that this nutrient crosses the mucosa by simple diffusion. Unidirectional influx of [3H]pantothenic acid (0.9 microM) across the brush-border membrane of rat jejunum in vitro demonstrates sodium dependence and saturation kinetics. Net transepithelial transport (absorption) of pantothenic acid takes place in everted sacs of jejunum against an electrochemical potential gradient. This accumulation does not occur in tissue exposed to metabolic inhibitors. Also, pantothenic acid accumulates in the transport cells of both rat and chicken intestine against a 9- to 10-fold concentration gradient. Recently absorbed pantothenic acid is freely diffusible from isolated chicken enterocytes. No metabolic conversion of pantothenic acid was detected during absorption in the intestine of either species under conditions in vitro or in vivo. The present results indicate that pantothenic acid present at low concentrations is absorbed in the intestine by a specific transport mechanism; the process is best described as sodium-dependent, secondary active transport.

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Kinetics of Various 99mTc-Sn-Pyrophosphate Compounds in the Rat

Nuklearmedizin ◽

10.1055/s-0037-1620623 ◽

1977 ◽

Vol 16 (04) ◽

pp. 157-162 ◽

Cited By ~ 1

Author(s):

C. Schümichen ◽

B. Mackenbrock ◽

G. Hoffmann

Keyword(s):

Normal Saline ◽

Half Life ◽

Compound A ◽

Short Half Life ◽

Low Concentrations ◽

The Stability ◽

Kinetics Of ◽

In Vitro Stability

SummaryThe bone-seeking 99mTc-Sn-pyrophosphate compound (compound A) was diluted both in vitro and in vivo and proved to be unstable both in vitro and in vivo. However, stability was much better in vivo than in vitro and thus the in vitro stability of compound A after dilution in various mediums could be followed up by a consecutive evaluation of the in vivo distribution in the rat. After dilution in neutral normal saline compound A is metastable and after a short half-life it is transformed into the other 99mTc-Sn-pyrophosphate compound A is metastable and after a short half-life in bone but in the kidneys. After dilution in normal saline of low pH and in buffering solutions the stability of compound A is increased. In human plasma compound A is relatively stable but not in plasma water. When compound B is formed in a buffering solution, uptake in the kidneys and excretion in urine is lowered and blood concentration increased.It is assumed that the association of protons to compound A will increase its stability at low concentrations while that to compound B will lead to a strong protein bond in plasma. It is concluded that compound A will not be stable in vivo because of a lack of stability in the extravascular space, and that the protein bond in plasma will be a measure of its in vivo stability.

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