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  • 11
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Comparative Biochemistry and Physiology -- Part B: Biochemistry and 45 (1973), S. 657-667 
    ISSN: 0305-0491
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 12
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Comparative Biochemistry and Physiology -- Part B: Biochemistry and 56 (1977), S. 249-254 
    ISSN: 0305-0491
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 13
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Comparative Biochemistry and Physiology -- Part B: Biochemistry and 67 (1980), S. 243-248 
    ISSN: 0305-0491
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 14
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Comparative Biochemistry and Physiology -- Part B: Biochemistry and 67 (1980), S. 249-256 
    ISSN: 0305-0491
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 15
    ISSN: 1432-1793
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The actions of exogenous arachidonic acid on the performance of the isolated and perfused systemic heart of Octopus vulgaris (collected in the Bay of Naples in 1992), and the potential of this heart for eicosanoid synthesis are described. Arachidonic acid induces positive chronotropic and inotropic effects. The positive inotropic effect is apparent only at the lowest concentration used (10−7 M) and in the paced heart preparations, in which a negative relationship between stroke volume and heart rate has been demonstrated. Using 10−5 M arachidonate, which induces the greatest chronotropic effect, a reduction of inotropism is evident which is due to the above negative relationship between stroke volume and heart rate. These effects are scarcely affected by the cyclooxygenase and lipoxygenase inhibitors, indomethacin (IM) and nordihydroguaiaretic acid (NDGA), respectively. On the coronary system of this heart arachidonic acid displays a potent vasoconstrictory action (ca. 100 percent increase of coronary resistance). This effect is potentiated by IM and reduced by NDGA. 14C-arachidonate is metabolized by the octopus ventricle homogenate into the lipoxygenase products (assayed as hydroxy acids) more actively than into cyclooxygenase products (prostanoids: PGE2, PGD2, PGF2α and 6-keto-PGF1α). On the other hand, the Ca-ionophore A23187 enhances the production of cyclooxygenase metabolites much more than of lipoxygenase metabolites.
    Type of Medium: Electronic Resource
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  • 16
    Electronic Resource
    Electronic Resource
    Springer
    Naturwissenschaften 72 (1985), S. 148-149 
    ISSN: 1432-1904
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Natural Sciences in General
    Type of Medium: Electronic Resource
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  • 17
    Electronic Resource
    Electronic Resource
    Springer
    Fish physiology and biochemistry 13 (1994), S. 249-261 
    ISSN: 1573-5168
    Keywords: rainbow trout ; perfused coronary non-working heart preparation ; catecholamines ; thromboxane ; prostacyclin ; coronary resistance
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract An isolated non-working trout heart, cannulated through the coronary artery and perfused with oxygenated saline with a coronary pressure head of 3.0 kPa has been used in this study. Effects on the coronar resistance of catecholamines, thromboxanes (TXs) and prostacyclin (PGI2) were analyzed. The effects of PGI2 and TXs in presence of noradrenaline were also evaluated. Both adrenaline and noradrenaline vasoconstrict the trout coronary system, noradrenaline being more potent than adrenaline. TXA2 induces 45% vasoconstriction at 10−6M, while TXB2 at the same concentration is a slight vasodilator. PGI2 acts as a weak vasodilator (about 20% decrease in resistance at 10−6M). In presence of 10−7M noradrenaline, 10−8M TXA2 reduces the vasoconstriction induced by the catecholamine alone from 60% to about 15%. Under similar conditions, 10−9M PGI2 potentiates the vasoconstrictive response induced by noradrenaline while a much higher PGI2 concentration (10−6M) completely abolishes the vasoconstriction. The β-receptor antagonist propranolol induces vasoconstriction, and 10−9M PGI2 in presence of propranolol further increases the vasoconstriction. The α-receptor antagonist phentolamine induces vasodilation and 10−9M PGI2 does not affect coronary resistance induced by phentolamine. These results imply a possible interaction between noradrenaline and prostanoids (TXs and PGI2) in the vasomotion of trout coronary system.
    Type of Medium: Electronic Resource
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  • 18
    Electronic Resource
    Electronic Resource
    Springer
    Journal of comparative physiology 167 (1997), S. 98-104 
    ISSN: 1432-136X
    Keywords: Key words   Acetylcholine  ;  l-Arginine  ;  Nitroprusside  ; NOS inhibitors  ;  Serotonin
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract The effects of l-arginine, and its analogues N ω-nitro-l-arginine methyl ester and N ω-nitro-l-arginine on vascular resistance were investigated in the intact coronary system of an isolated non-working trout heart preparation. l-Arginine, at 10–8 mol · l–1induced a slight vasodilatory effect (max 10%). N ω-nitro-l-arginine methyl ester and N ω-Nitro-l-arginine in the range 10–8–10–4 mol · l–1 caused dose-dependent increases in coronary resistance. The vasodilatory action of l-arginine was abolished when the preparation was pretreated with 10–4 mol · l–1 N ω-nitro-l-arginine or N ω-nitro-l-arginine methyl ester. Nitroprusside alone at 1 mmol · l–1 induced a maximum vasodilation (30%) of the coronary system. Methylene blue a known inhibitor of guanylate cyclase, induced a strong vasoconstriction (already significant at 10–5 mol · l–1) and was able to overcome the vasodilative effect of nitroprusside. The endothelial nitric oxide agonists acetylcholine and serotonin, established in mammalian vessels, also mediate vasodilation in trout coronary system. In 50% of preparations, acetylcholine induced a biphasic response with vasodilation at low concentration (max 15% at 10–8 mol · l–1). Serotonin displayed a dose-response vasodilation in the range 10–8–10–4 mol · l–1 (max 20%). These vasodilative effects were reduced or abolished by 10–4 mol · l–1 l-NA. These data support the existence of NO-mediated vasodilation mechanisms in the trout coronary system.
    Type of Medium: Electronic Resource
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  • 19
    ISSN: 1432-136X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary 1. Phosphoenolpyruvate carboxykinase from four facultative anaerobic invertebrate species is shown to decarboxylate oxalacetate to phosphoenolpyruvate (Table 1). Knowledge of this reaction is of importance in the evaluation of gluconeogenic capacities of these organisms. 2. InTubifex the PEPCK-catalyzed decarboxylation reaction was characterized and its regulatory properties were studied. PEPCK mainly occurs in the cytosolic fraction and its absolute requirements in the decarboxylation direction are oxalacetate, Mn2+, nucleoside triphosphate (ITP) (Table 2). The pH optima for PEPCK-catalyzed decarboxylation and carboxylation reactions are 8.1 and 7.1, respectively (Fig. 1).K m values for oxalacetate and ITP were 0.25 and 0.39 mM, respectively (Fig. 2b and c). In presence of 0.5 mM AMP, the decarboxylation reaction was inhibited up to 50% of the control while even in presence of 5 mM AMP, the carboxylation reaction was unaffected (Fig. 3). Lombricine phosphate, one of the naturally occurring phosphagens inTubifex, activates the PEPCK-catalyzed decarboxylation reaction. 3-Mercaptopicolinic acid, a known specific inhibitor of vertebrate and invertebrate PEPCKs, also inhibitsTubifex PEPCK (Table 3). 3. UnlikeCrassostrea andAscaris, pyruvate carboxylase activity is present inTubifex tissues which will facilitate the conversion of C3 to C4 compounds and thus their eventual incorporation into glycogen. 4. Various gluconeogenic precursors when provided exogenously under aerobic conditions are incorporated into tissue glycogen by the intactTubifex (Table 4). 5. The potential roles of PEPCK regulatory properties under aerobic and anaerobic conditions are discussed with relation to gluconeogenesis and glycolysis inTubifex.
    Type of Medium: Electronic Resource
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  • 20
    ISSN: 1432-136X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary 1. During anaerobic exposure ofTubifex, lactate and alanine increase only within the first 24 h, while concentrations of succinate, propionate and also acetate continually increase under prevailing anaerobic conditions. Enzymes involved in anaerobic energy metabolism were isolated, and the effects of various metabolites and inorganic compounds on their catalytic properties studied. 2. The specific activities of the cytosolic enzymes LDH, PK, MDH, and PEPCK, and of mitochondrial malic enzyme and MDH are high. 3. Under conditions of high HCO 3 − (HCO 3 − +CO2 system), PEPCK is maximally active while PK is inhibited. 4. The catalytic properties of mitochondrial malic enzyme indicate that in vivo this enzyme operates in the direction of malate decarboxylation. 5. The cytosolic oxidoreductases LDH and MDH were examined with regard to the maintenance of redox state. Function of MDH is only subject to substrate availability, while the enzyme-substrate affinity of LDH might be affected by pH to a limited extent. 6. The data support the conclusion that total CO2, fructose-1,6-diphosphate concentration, the adenylate energy charge, and-only to a limited extent-the intracellular pH are regulatory signals which govern PEP metabolism inTubifex.
    Type of Medium: Electronic Resource
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