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  • 1975-1979  (2)
  • Ca2+ dependency  (1)
  • Manganese  (1)
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  • 1975-1979  (2)
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  • 1
    ISSN: 1432-2013
    Keywords: Parotid ; Amylase secretion ; Calcium ; Manganese ; α- and β-Adrenoceptor ; Acetylcholine
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary 1. The output of amylase from superfused mouse parotid segments was monitored by an on-line automated fluorometric method. 2. During exposure to Ca2+-free solution, containing the Ca2+-chelating agent EGTA, excitation of α-adrenoceptors or cholinergic receptors only resulted in a very small and transient increase in amylase output. Admission of Ca2+ during sustained stimulation caused a marked rise in amylase output which was sustained. 3. During exposure to Ca2+-free solution containing EGTA excitation of β-adrenoceptors caused the usual very marked rise in amylase output and the enhanced amylase secretion was sustained. Admission of Ca2+ during sustained isoprenaline stimulation only caused a small transient rise in amylase output. 4. The effect of ACh on amylase output varied with the extracellular Ca2+ concentration, being reduced at subnormal extracellular levels and enhanced during superfusion with fluid containing 20 mM Ca2+. 5. 5 mM Mn2+ acted as a stimulant of amylase secretion even in the presence of blocking agents for the cholinergic, α- and β-adrenergic receptor sites. The effect of Mn2+ was biphasic; an initial transient increase in amylase output followed by a slowly developing sustained increase in secretion. The initial response was abolished after pretreatment with EGTA in a Ca2+-free solution. 6. Adding Mn2+ (5 mM) just after addition of ACh had caused maximal amylase secretion resulted in an immediate reduction in amylase output. Adding Mn2+ and ACh simultaneously to the superfusion solution resulted in a response smaller than that expected for ACh alone. The effect of ACh during continued exposure to Mn2+ (5 mM) was greatly reduced compared to control conditions. Stimulation with Mn2+ during continued exposure to isoprenaline resulted in a marked transient increase in amylase output. 7. The action of stimulants exciting cholinergic and α-adrenergic receptors is entirely dependent on extracellular Ca2+ whereas the action of stimulants exciting adrenergic β-receptors is relatively independent of Ca2+. Mn2+ immediately inhibits ACh-evoked amylase secretion probably by reducing Ca2+-influx. Mn2+ is, however also a stimulant of amylase secretion probably acting by displacing membrane-bound cell Ca2+.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Pflügers Archiv 370 (1977), S. 179-183 
    ISSN: 1432-2013
    Keywords: Pancreas ; Fluid secretion ; Amylase secretion ; Ca2+ dependency ; Caerulein ; Secretin
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary In the perfused rat pancreas fluid and amylase secretion was measured in the absence of stimulation and during stimulation with caerulein or secretin. Taking away perfusion fluid Ca2+ only slightly reduced spontaneous fluid secretion, but caused a marked reduction in the amylase output. In experiments where the CO2/HCO 3 − -buffer had been replaced by a tris buffer removal of perfusion fluid Ca2+ abolished spontaneous fluid and amylase secretion. Taking away perfusion fluid Ca2+ during continuous stimulation with caerulein caused an immediate rapid reduction in fluid and amylase secretion which was reversible upon readmission of Ca2+. Removal of perfusion fluid Ca2+ and addition of EGTA during stimulation with secretin had no effect on fluid secretion for the first half an hour after start of Ca2+ deprivation. Thereafter a gradual reduction in fluid flow occurred which was non-reversible upon Ca2+ readmission. During stimulation with monobutyryl cyclic AMP Ca2+-deprivation failed to reduce fluid secretion within a period of half an hour. Augmenting the perfusion fluid [Ca2+] to 20 mM during stimulation with caerulein caused a sharp reduction in fluid secretion and a small decrease in amylase output. These effects were partially reversible if the period of exposure to the high Ca2+ solution was less than 20 min. It is concluded that extracellular Ca2+ is important for caerulein-evoked but not for secretin-evoked fluid secretion.
    Type of Medium: Electronic Resource
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