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1.
Arch Insect Biochem Physiol ; 74(2): 114-26, 2010 Jun.
Article in English | MEDLINE | ID: mdl-20513059

ABSTRACT

A dose-dependent inhibition of endogenous trypsin and aminopeptidase occurs in the lumen of Spodoptera frugiperda after feeding L6 larvae exogenous inhibitors soybean trypsin inhibitor (SBTI), tosyl-L-lysine chloromethyl ketone-HCl (TLCK), or bestatin, respectively, for 3 days. TLCK inhibits trypsin in tissue extracts and in secretions more strongly than SBTI. The aminopeptidase released into the lumen (containing the peritrophic membrane) is strongly inhibited by bestatin, but the membrane-bound enzyme is not. A bound enzyme may be more resistant to an inhibitor than unbound. A cross-class elevation of aminopeptidase activity occurs in response to ingested trypsin inhibitor, but there was no cross-class effect of aminopeptidase inhibitor (bestatin) on trypsin activity. An endogenous trypsin and aminopeptidase inhibitor is present in the lumen and ventricular cells. The strength of the endogenous trypsin inhibition seems to be in the same range as that resulting from ingestion of the exogenous inhibitor SBTI. In some insect species, considerable trypsin secretion occurs in unfed as well as in fed animals, and endogenous protease inhibitors might function to protect the ventricular epithelium by inactivation of trypsin when less food is available.


Subject(s)
Aminopeptidases/antagonists & inhibitors , Spodoptera/metabolism , Trypsin Inhibitors/genetics , Trypsin Inhibitors/metabolism , Aminopeptidases/metabolism , Animals , Larva/genetics , Larva/metabolism , Spodoptera/drug effects , Spodoptera/genetics , Trypsin/metabolism , Trypsin Inhibitors/pharmacology
2.
Arch Insect Biochem Physiol ; 73(1): 14-29, 2010 Jan.
Article in English | MEDLINE | ID: mdl-19771560

ABSTRACT

There is a basal level of enzyme activity for trypsin, aminopeptidase, amylase, and lipase in the gut of unfed larval (L6) Spodoptera frugiperda. Trypsin activity does not decrease with non-feeding, possibly because of the low protein levels in plants along with high amino acid requirements for growth and storage (for later reproduction in adults). Therefore, trypsin must always be present so that only a minimal protein loss via egestion occurs. Larvae, however, adjust amylase activity to carbohydrate ingestion, and indeed amylase activity is five-fold higher in fed larvae compared to unfed larvae. Gut lipase activity is low, typical of insects with a high carbohydrate diet. A flat-sheet preparation of the ventriculus was used to measure the release of enzymes in response to specific nutrients and known brain/gut hormones in S. frugiperda. Sugars greatly increase (>300%) amylase release, but starch has no effect. Proteins and amino acids have little or no effect on trypsin or aminopeptidase release. The control of enzyme release in response to food is likely mediated through neurohormones. Indeed, an allatostatin (Spofr-AS A5) inhibits amylase and trypsin, and allatotropin (Manse- AT) stimulates amylase and trypsin release. Spofr-AS A5 also inhibits ileum myoactivity and Manse-AT stimulates myoactivity. The epithelial secretion rate of amylase and trypsin was about 20% of the amount of enzyme present in the ventricular lumen, which, considering the efficient counter-current recycling of enzymes, suggests that the secretion rate is adequate to replace egested enzymes.


Subject(s)
Aminopeptidases/metabolism , Amylases/metabolism , Digestive System/enzymology , Insect Hormones/metabolism , Insect Proteins/metabolism , Larva/physiology , Lipase/metabolism , Neuropeptides/metabolism , Neurotransmitter Agents/metabolism , Spodoptera/physiology , Trypsin/metabolism , Animals , Food , Ileum/metabolism , In Vitro Techniques , Larva/anatomy & histology , Muscle, Smooth/physiology
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