@article{MuschiolikDraegerRaweletal.1995, author = {Muschiolik, Gerald and Dr{\"a}ger, Silke and Rawel, Harshadrai Manilal and Gunning, Paul and Clark, David C.}, title = {Preliminary investigations of the functions of whey protein preparations in O/W systems}, year = {1995}, language = {en} } @article{StarkWalzelOzierenskietal.1995, author = {Stark, Claudia and Walzel, Erwin and Ozierenski, B{\"a}rbel and Kroll, J{\"u}rgen}, title = {Die Wirkung von Pektin bei aktueller Bleiexposition}, year = {1995}, language = {de} } @article{StarkWalzelDongowskietal.1995, author = {Stark, Claudia and Walzel, Erwin and Dongowski, Gerhard and Ozierenski, B{\"a}rbel}, title = {Influence of pectin on lead incorporation in germ-free and conventionalized rats}, year = {1995}, language = {en} } @article{WalzelKroll1995, author = {Walzel, Erwin and Kroll, J{\"u}rgen}, title = {Kritische Spurenelemente in der Ern{\"a}hrung}, year = {1995}, language = {de} } @article{SchneiderWalzel1995, author = {Schneider, Elisabeth and Walzel, Erwin}, title = {Kritische Mineralstoffe in der Schwangerschaft sowie im S{\"a}uglings- und Kleinkindalter : Magnesium, Zink und Selen}, year = {1995}, language = {de} } @article{SchneiderWalzel1995, author = {Schneider, Elisabeth and Walzel, Erwin}, title = {Kritische Mineralstoffe in der Schwangerschaft sowie im S{\"a}uglings- und Kleinkindalter : Fluoride}, year = {1995}, language = {de} } @article{SchneiderWalzel1995, author = {Schneider, Elisabeth and Walzel, Erwin}, title = {Kritische Mineralstoffe in der Schwangerschaft sowie im S{\"a}uglings- und Kleinkindalter : Eisen}, year = {1995}, language = {de} } @article{SchneiderWalzel1995, author = {Schneider, Elisabeth and Walzel, Erwin}, title = {Kritische Mineralstoffe in der Schwangerschaft sowie im S{\"a}uglings- und Kleinkindalter : Calcium}, year = {1995}, language = {de} } @book{OPUS4-27408, title = {Aroma perception, formation, evaluation : proceedings of the 4th Wartburg Aroma Symposium}, editor = {Rothe, Manfred and Kruse, Hans-Peter}, publisher = {Eigenverl.}, address = {Bergholz-Rehbr{\"u}cke}, pages = {712 S.}, year = {1995}, language = {en} } @article{RawelKroll1995, author = {Rawel, Harshadrai Manilal and Kroll, J{\"u}rgen}, title = {Some aspects of reactions of benzyl isothiocyanate with bovine sarcoplasmic proteins}, year = {1995}, language = {en} } @article{RawelMuschiolik1995, author = {Rawel, Harshadrai Manilal and Muschiolik, Gerald}, title = {Changes in molecular structure and functionality during purification and denaturation of faba bean protein}, year = {1995}, language = {en} } @article{OzierenskiStarkWalzel1995, author = {Ozierenski, B{\"a}rbel and Stark, Claudia and Walzel, Erwin}, title = {Effects of pectin on lead-specific biomarkers and hepatic and extra hepatic biotransformation enzymes in lead- exposed rats}, year = {1995}, language = {en} } @article{MuellerRawelMuschiolik1995, author = {M{\"u}ller, Silke and Rawel, Harshadrai Manilal and Muschiolik, Gerald}, title = {Surface activity of modified soy proteins}, year = {1995}, language = {en} } @article{KruseKroll1995, author = {Kruse, Hans-Peter and Kroll, J{\"u}rgen}, title = {Fettaustauscher : lebensmittelchemische und ern{\"a}hrungsphysiologische Aspekte}, year = {1995}, language = {de} } @article{DraegerMuschiolikRawel1995, author = {Dr{\"a}ger, Silke and Muschiolik, Gerald and Rawel, Harshadrai Manilal}, title = {Molecular and emulsifying behaviour of pea proteins}, year = {1995}, language = {en} } @article{DraegerMuschiolikRawel1995, author = {Dr{\"a}ger, Silke and Muschiolik, Gerald and Rawel, Harshadrai Manilal}, title = {Behaviour of whey protein stabilised emulsions}, year = {1995}, language = {en} } @misc{HespelingPueschelJungermannetal.1995, author = {Hespeling, Ursula and P{\"u}schel, Gerhard Paul and Jungermann, Kurt and G{\"o}tze, Otto and Zwirner, J{\"o}rg}, title = {Stimulation of glycogen phosphorylase in rat hepatocytes via prostanoid release from Kupffer cells by recombinant rat anaphylatoxin C5a but not by native human C5a in hepatocyte/Kupffer cell co-cultures}, url = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-45909}, year = {1995}, abstract = {Human anaphylatoxin C3a had previously been shown to increase glycogenolysis in perfused rat liver and prostanoid formation in rat liver macrophages. Surprisingly, human C5a, which in other systems elicited stronger responses than C3a, did not increase glycogenolysis in perfused rat liver. Species incompatibilities within the experimental system had been supposed to be the reason. The current study supports this hypothesis: (1) In rat liver macrophages that had been maintained in primary culture for 72 h recombinant rat anaphylatoxin C5a in concentrations between 0.1 and 10 pg/ml increased the formation of thromboxane A₂, prostaglandin D₂, E₂ and F₂α6- to 12-fold over basal within 10 min. In contrast, human anaphylatoxin C5a did not increase prostanoid formation in rat Kupffer cells. (2) The increase in prostanoid formation by recombinant rat C5a was specific. It was inhibited by a neutralizing monoclonal antibody. (3) In co-cultures of rat hepatocytes and rat Kupffer cells but not in hepatocyte mono-cultures recombinant rat C5a increased glycogen phosphorylase activity 3-fold over basal. This effect was inhibited by incubation of the co-cultures with 500 μM acetylsalicyclic acid. Thus, C5a generated either locally in the liver or systemically e.g. in the course of sepsis, may increase hepatic glycogenolysis by a prostanoid-mediated intercellular communication between Kupffer cells and hepatocytes.}, language = {en} } @misc{HespelingJungermannPueschel1995, author = {Hespeling, Ursula and Jungermann, Kurt and P{\"u}schel, Gerhard Paul}, title = {Feedback-inhibition of glucagon-stimulated glycogenolysis in hepatocyte/kupffer cell cocultures by glucagon-elicited prostaglandin production in kupffer cells}, url = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-16697}, year = {1995}, abstract = {Prostaglandins, released from Kupffer cells, have been shown to mediate the increase in hepatic glycogenolysis by various stimuli such as zymosan, endotoxin, immune complexes, and anaphylotoxin C3a involving prostaglandin (PG) receptors coupled to phospholipase C via a G(0) protein. PGs also decreased glucagon-stimulated glycogenolysis in hepatocytes by a different signal chain involving PGE(2) receptors coupled to adenylate cyclase via a G(i) protein (EP(3) receptors). The source of the prostaglandins for this latter glucagon-antagonistic action is so far unknown. This study provides evidence that Kupffer cells may be one source: in Kupffer cells, maintained in primary culture for 72 hours, glucagon (0.1 to 10 nmol/ L) increased PGE(2), PGF(2 alpha), and PGD(2) synthesis rapidly and transiently. Maximal prostaglandin concentrations were reached after 5 minutes. Glucagon (1 nmol/L) elevated the cyclic adenosine monophosphate (cAMP) and inositol triphosphate (InsP(3)) levels in Kupffer cells about fivefold and twofold, respectively. The increase in glyco gen phosphorylase activity elicited by 1 nmol/L glucagon was about twice as large in monocultures of hepatocytes than in cocultures of hepatocytes and Kupffer cells with the same hepatocyte density. Treatment of cocultures with 500 mu mol/L acetylsalicylic acid (ASA) to irreversibly inhibit cyclooxygenase (PGH-synthase) 30 minutes before addition of glucagon abolished this difference. These data support the hypothesis that PGs produced by Kupffer cells in response to glucagon might participate in a feedback loop inhibiting glucagon-stimulated glycogenolysis in hepatocytes.}, language = {en} }