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  • 1955-1959  (10)
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  • 1955-1959  (10)
Year
Subjects(RVK)
  • 1
    Online Resource
    Online Resource
    American Physiological Society ; 1957
    In:  Journal of Applied Physiology Vol. 11, No. 2 ( 1957-09), p. 143-147
    In: Journal of Applied Physiology, American Physiological Society, Vol. 11, No. 2 ( 1957-09), p. 143-147
    Type of Medium: Online Resource
    ISSN: 8750-7587 , 1522-1601
    RVK:
    RVK:
    Language: English
    Publisher: American Physiological Society
    Publication Date: 1957
    detail.hit.zdb_id: 1404365-8
    SSG: 12
    SSG: 31
    Location Call Number Limitation Availability
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  • 2
    Online Resource
    Online Resource
    American Physiological Society ; 1956
    In:  American Journal of Physiology-Legacy Content Vol. 188, No. 1 ( 1956-12-31), p. 66-70
    In: American Journal of Physiology-Legacy Content, American Physiological Society, Vol. 188, No. 1 ( 1956-12-31), p. 66-70
    Abstract: The addition of pectin and a protopectin preparation containing galactose and arabinose to a noncholesterol-containing basal diet increased the fecal excretion of saponifiable lipids; the absorption of endogenous cholesterol and the excretion of nonsaponifiable lipids were uninfluenced. The addition of pectin to a basal diet containing cholesterol increased the excretion of fecal saponifiable and nonsaponifiable lipids and decreased the absorption of exogenous cholesterol. The addition of the protopectin preparation to the same diet had no significant effect on the excretion of saponifiable lipids, but the excretion of cholesterol was decidely reduced and, in two experiments out of three, there occurred an approximately equivalent increase in noncholesterol nonsaponifiable material. The addition of gum arabic or arabinose to this ration produced practically no changes in the amount of saponifiable and nonsaponifiable fecal lipids and in the recovery of exogenous cholesterol in the feces. Only very small quantities of noncolor-developing sterols were eliminated either on the cholesterol basal diet or when this diet was supplemented with pectin, protopectin, gum arabic or arabinose.
    Type of Medium: Online Resource
    ISSN: 0002-9513
    RVK:
    RVK:
    Language: English
    Publisher: American Physiological Society
    Publication Date: 1956
    detail.hit.zdb_id: 1477334-X
    detail.hit.zdb_id: 2065807-2
    detail.hit.zdb_id: 1477287-5
    detail.hit.zdb_id: 1477308-9
    detail.hit.zdb_id: 1477297-8
    detail.hit.zdb_id: 1477331-4
    detail.hit.zdb_id: 1477300-4
    detail.hit.zdb_id: 1477329-6
    SSG: 12
    Location Call Number Limitation Availability
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  • 3
    Online Resource
    Online Resource
    American Physiological Society ; 1956
    In:  American Journal of Physiology-Legacy Content Vol. 188, No. 1 ( 1956-12-31), p. 61-65
    In: American Journal of Physiology-Legacy Content, American Physiological Society, Vol. 188, No. 1 ( 1956-12-31), p. 61-65
    Abstract: A fat balance study was conducted on 12 rats with and 12 without exclusion of the pancreatic juice, using tripalmitin, trielaidin, triolein, tallow and corn oil, or fats varying in regard to melting point, saturation, and cis and trans isomerism. Exclusion of pancreatic juice decreased the utilization of these fats. The decrement ranged from 14 to 18% of the intake of the different fats when fed at a level of 8% of the dry weight of the diet. The extent of impairment expressed as millimols could not be correlated with the physical and chemical characteristics of the fats; but if expressed as percentage of fat absorbed, the impairment was related to the melting point of the fat. The fecal elimination of soap was increased significantly by the exclusion of pancreatic juice in the case of corn oil, triolein and tallow; was not significantly increased in the case of trielaidin; and was decreased in the case of tripalmitin, due probably to decreased hydrolysis. Exclusion of pancreatic juice increased the elimination of endogenous total lipid and of soap. Fat utilization was correlated more closely with the melting point of the fats than with their saturation, suggesting that the melting point is concerned in determining utilization more than any other characteristic of the fat.
    Type of Medium: Online Resource
    ISSN: 0002-9513
    RVK:
    RVK:
    Language: English
    Publisher: American Physiological Society
    Publication Date: 1956
    detail.hit.zdb_id: 1477334-X
    detail.hit.zdb_id: 2065807-2
    detail.hit.zdb_id: 1477287-5
    detail.hit.zdb_id: 1477308-9
    detail.hit.zdb_id: 1477297-8
    detail.hit.zdb_id: 1477331-4
    detail.hit.zdb_id: 1477300-4
    detail.hit.zdb_id: 1477329-6
    SSG: 12
    Location Call Number Limitation Availability
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  • 4
    Online Resource
    Online Resource
    American Physiological Society ; 1956
    In:  American Journal of Physiology-Legacy Content Vol. 186, No. 2 ( 1956-08-01), p. 231-238
    In: American Journal of Physiology-Legacy Content, American Physiological Society, Vol. 186, No. 2 ( 1956-08-01), p. 231-238
    Abstract: Aminoguanidine, a diamine oxidase inhibitor, in a dose of 0.4–1.0 mg/kg/ min. given intravenously during a period of from 20–25 minutes stimulates the gastric acid secretory mechanism of a Heidenhain and Ivy pouch dog secreting no free acid after a latent period of from 20–30 minutes for a period of 1–4 hours, depending on the dose. A rough dose-response relationship exists until evidences of toxicity occur at a dose of 4–5 mg/kg/min. is given. The administration of an intravenous threshold dose of aminoguanidine decidedly augments the gastric secretory response to a 0.05-mg dose of histamine diphosphate given subcutaneously to such dogs every 10 minutes. The existing evidence suggests that the augmentory effect is an additive effect due to the accumulation of histamine resulting from the action of aminoguanidine on histaminase.
    Type of Medium: Online Resource
    ISSN: 0002-9513
    RVK:
    RVK:
    Language: English
    Publisher: American Physiological Society
    Publication Date: 1956
    detail.hit.zdb_id: 1477334-X
    detail.hit.zdb_id: 2065807-2
    detail.hit.zdb_id: 1477287-5
    detail.hit.zdb_id: 1477308-9
    detail.hit.zdb_id: 1477297-8
    detail.hit.zdb_id: 1477331-4
    detail.hit.zdb_id: 1477300-4
    detail.hit.zdb_id: 1477329-6
    SSG: 12
    Location Call Number Limitation Availability
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  • 5
    Online Resource
    Online Resource
    American Physiological Society ; 1957
    In:  American Journal of Physiology-Legacy Content Vol. 190, No. 2 ( 1957-08-01), p. 214-220
    In: American Journal of Physiology-Legacy Content, American Physiological Society, Vol. 190, No. 2 ( 1957-08-01), p. 214-220
    Abstract: The exclusion of pancreatic juice had no significant effect on elimination of endogenous cholesterol in the rat but increased it slightly in three dogs. Forty per cent of the dietary cholesterol was absorbed without and with pancreatic exclusion in the presence of a fat-free diet. Hence, pancreatic juice is not specifically necessary for the absorption of cholesterol. Pancreatic exclusion had no effect on the absorption of either dietary cholesterol or fatty acid, or both, when oleic and palmitic acid were fed. This indicates that any effect pancreatic exclusion may exert on cholesterol absorption when a fat containing diet is fed depends on the change in the utilization of the fat resulting from the exclusion. In the case of corn oil, triolein, trielaidin and tallow but not with tripalmitin, pancreatic exclusion was followed by an increased fecal elimination of both fatty acid and cholesterol. The increment of fatty acid elimination was large enough to dissolve the excess cholesterol excreted in the rats with pancreatic exclusion, except in the case of trielaidin. The only statistically significant decrease in the absorption of dietary cholesterol which resulted from pancreatic exclusion occurred when one of the unsaturated fatty acid esters, namely, corn oil, triolein, or trielaidin was the fat fed. These observations fail to show that pancreatic cholesterol esterase plays a specifically essential role in the absorption of free dietary cholesterol.
    Type of Medium: Online Resource
    ISSN: 0002-9513
    RVK:
    RVK:
    Language: English
    Publisher: American Physiological Society
    Publication Date: 1957
    detail.hit.zdb_id: 1477334-X
    detail.hit.zdb_id: 2065807-2
    detail.hit.zdb_id: 1477287-5
    detail.hit.zdb_id: 1477308-9
    detail.hit.zdb_id: 1477297-8
    detail.hit.zdb_id: 1477331-4
    detail.hit.zdb_id: 1477300-4
    detail.hit.zdb_id: 1477329-6
    SSG: 12
    Location Call Number Limitation Availability
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  • 6
    Online Resource
    Online Resource
    American Physiological Society ; 1957
    In:  Journal of Applied Physiology Vol. 11, No. 1 ( 1957-07), p. 1-7
    In: Journal of Applied Physiology, American Physiological Society, Vol. 11, No. 1 ( 1957-07), p. 1-7
    Type of Medium: Online Resource
    ISSN: 8750-7587 , 1522-1601
    RVK:
    RVK:
    Language: English
    Publisher: American Physiological Society
    Publication Date: 1957
    detail.hit.zdb_id: 1404365-8
    SSG: 12
    SSG: 31
    Location Call Number Limitation Availability
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  • 7
    Online Resource
    Online Resource
    Wiley ; 1957
    In:  Acta Physiologica Scandinavica Vol. 38, No. 3-4 ( 1957-08), p. 207-219
    In: Acta Physiologica Scandinavica, Wiley, Vol. 38, No. 3-4 ( 1957-08), p. 207-219
    Type of Medium: Online Resource
    ISSN: 0001-6772 , 1365-201X
    URL: Issue
    RVK:
    Language: English
    Publisher: Wiley
    Publication Date: 1957
    detail.hit.zdb_id: 2012166-0
    detail.hit.zdb_id: 2219379-0
    SSG: 12
    Location Call Number Limitation Availability
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  • 8
    Online Resource
    Online Resource
    American Physiological Society ; 1955
    In:  American Journal of Physiology-Legacy Content Vol. 181, No. 2 ( 1955-05-01), p. 439-440
    In: American Journal of Physiology-Legacy Content, American Physiological Society, Vol. 181, No. 2 ( 1955-05-01), p. 439-440
    Type of Medium: Online Resource
    ISSN: 0002-9513
    RVK:
    RVK:
    Language: English
    Publisher: American Physiological Society
    Publication Date: 1955
    detail.hit.zdb_id: 1477334-X
    detail.hit.zdb_id: 2065807-2
    detail.hit.zdb_id: 1477287-5
    detail.hit.zdb_id: 1477308-9
    detail.hit.zdb_id: 1477297-8
    detail.hit.zdb_id: 1477331-4
    detail.hit.zdb_id: 1477300-4
    detail.hit.zdb_id: 1477329-6
    SSG: 12
    Location Call Number Limitation Availability
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  • 9
    Online Resource
    Online Resource
    American Physiological Society ; 1956
    In:  American Journal of Physiology-Legacy Content Vol. 186, No. 2 ( 1956-08-01), p. 239-244
    In: American Journal of Physiology-Legacy Content, American Physiological Society, Vol. 186, No. 2 ( 1956-08-01), p. 239-244
    Abstract: 1-Isonicotinyl-2-isopropylhydrazine, ‘Marsilid,’ and isonicotinylhydrazine, ‘Rimifon,’ stimulate gastric secretion in a Heidenhain and Ivy transplanted pouch dog when given intravenously during the fasting basal state. The secretory threshold for these compounds, especially ‘Rimifon,’ is close to a toxic dose. Aminoguanidine given intravenously stimulates gastric secretion in the anesthetized dog and cat in doses which do not reduce blood pressure and do not give rise to evidences of toxicity. In the Heidenhain and Ivy transplanted pouch dog an intravenous threshold dose of aminoguanidine, an inhibitor of histaminase or histamine metabolizing enzyme I, decidedly augments the gastric secretory response to a small test-meal, even when the test-meal contains little or no histamine. Assuming on the basis of evidence published by Schayer and his colleagues (13–16) that aminoguanidine does not act directly on the parietal cell, it is concluded that histamine (or a substance inactivated by diamine oxidase) acts directly and physiologically to stimulate gastric secretion either by being released into the blood stream or by being released in the region of the parietal cell by a nonhistamine gastrin.
    Type of Medium: Online Resource
    ISSN: 0002-9513
    RVK:
    RVK:
    Language: English
    Publisher: American Physiological Society
    Publication Date: 1956
    detail.hit.zdb_id: 1477334-X
    detail.hit.zdb_id: 2065807-2
    detail.hit.zdb_id: 1477287-5
    detail.hit.zdb_id: 1477308-9
    detail.hit.zdb_id: 1477297-8
    detail.hit.zdb_id: 1477331-4
    detail.hit.zdb_id: 1477300-4
    detail.hit.zdb_id: 1477329-6
    SSG: 12
    Location Call Number Limitation Availability
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  • 10
    Online Resource
    Online Resource
    American Physiological Society ; 1957
    In:  American Journal of Physiology-Legacy Content Vol. 189, No. 1 ( 1957-03-31), p. 113-116
    In: American Journal of Physiology-Legacy Content, American Physiological Society, Vol. 189, No. 1 ( 1957-03-31), p. 113-116
    Abstract: Tripalmitin, a saturated, and triolein, an unsaturated fat, and their respective fatty acids were fed at a level of 8% by dry weight of the diet to 12 sham operated control and 12 pancreatic duct ligated rats. It was found that exclusion of pancreatic juice significantly decreased the utilization of both triolein and tripalmitin. Thus, the pancreatic juice is essential for the utilization of both saturated and unsaturated fat. It was found also that exclusion of pancreatic juice did not influence the absorption of oleic and palmitic acid. Therefore, it is concluded that pancreatic alkali does not exert any significant effect on the absorption of fatty acid in the amounts fed whether saturated or unsaturated, and that pancreatic lipase and/or the facilitation by pancreatic alkali of the hydrolysis of fat by any lipase present in the intestine is the factor (or factors) in pancreatic juice which is essential for the complete utilization of both saturated and unsaturated fat. The observed decrease in the utilization of tripalmitin produced by the exclusion of pancreatic juice was not larger than the decrease in the utilization of triolein; therefore, it is concluded that a desaturation of fat by a pancreatic dehydrogenase is not essential for the absorption of saturated fat.
    Type of Medium: Online Resource
    ISSN: 0002-9513
    RVK:
    RVK:
    Language: English
    Publisher: American Physiological Society
    Publication Date: 1957
    detail.hit.zdb_id: 1477334-X
    detail.hit.zdb_id: 2065807-2
    detail.hit.zdb_id: 1477287-5
    detail.hit.zdb_id: 1477308-9
    detail.hit.zdb_id: 1477297-8
    detail.hit.zdb_id: 1477331-4
    detail.hit.zdb_id: 1477300-4
    detail.hit.zdb_id: 1477329-6
    SSG: 12
    Location Call Number Limitation Availability
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