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1.
Peptides ; 34(1): 258-61, 2012 Mar.
Article in English | MEDLINE | ID: mdl-21524674

ABSTRACT

The effects of analogs of the diuretic peptides Locmi-DH, Dippu-DH(46) and Dippu-DH(31) on two aspects of appetitive behavior are investigated in previously food-deprived nymphs of Locusta migratoria. The analogs tested are the C-terminal 15-mer and nonapeptides and their corresponding cyclic analogs. At a nominal dose of 1pmol injected per nymph, the linear fragments and their cyclic analogs of Dippu-DH(46) display no significant effects on the latency to feed or on the length of the first meal in nymphs. However, at the same dose, the linear fragments of Dippu-DH(31) and their cyclic analogs, and analogs of Locmi-DH modulate appetitive behavior: they are anorexigenic in reducing the duration of the first meal, and generally increasing the latency to feed. The cyclic analogs of Dippu-DH(31) are at least as effective as their linear counterparts in influencing these aspects of appetitive behavior in locust nymphs.


Subject(s)
Appetitive Behavior/drug effects , Insect Hormones/chemistry , Insect Hormones/pharmacology , Locusta migratoria/drug effects , Peptides/chemistry , Peptides/pharmacology , Amino Acid Sequence , Animals , Diuretics/chemistry , Diuretics/pharmacology , Molecular Sequence Data
2.
Peptides ; 30(3): 603-7, 2009 Mar.
Article in English | MEDLINE | ID: mdl-18760318

ABSTRACT

We have investigated the effect of analogs of the two Dippu diuretic hormones, Dippu-DH(46) and Dippu-DH(31), on fluid secretion by Malpighian tubules of male Diploptera punctata. We synthesized analogs containing the amino acid methyl-homoserine, to replace methionine residues, to render these modified peptides less subject to oxidation. We have also synthesized C-terminal fragments and their corresponding cyclic analogs to determine their effect on fluid secretion in D. punctata. Our results indicate that the modified peptides retain significant activity in the Ramsay secretion assay. The linear fragments displayed no activity or some inhibitory activity whereas the cyclic analog fragments showed stimulatory activity, in the case of DH(46), or slight inhibitory activity, in the case of DH(31).


Subject(s)
Insect Hormones/chemical synthesis , Insect Proteins/chemical synthesis , Peptides, Cyclic/chemical synthesis , Amino Acid Sequence , Animals , Cockroaches , Diuretics/pharmacology , Insect Hormones/pharmacology , Insect Proteins/pharmacology , Male , Malpighian Tubules/drug effects , Malpighian Tubules/metabolism , Peptides, Cyclic/pharmacology
3.
Peptides ; 24(10): 1607-13, 2003 Oct.
Article in English | MEDLINE | ID: mdl-14706540

ABSTRACT

The synthesis is described of an analogue of the locust CRF-like diuretic peptide in which methionine in positions 1,3, and 13 is replaced by isosteric methyl-homoserine residues. This analogue has been tested for biological activity on Malpighian tubules in vitro, and feeding behavior in vivo. It is highly active in stimulating fluid secretion and accumulation of cAMP in tubules, and on increasing the latency to feed and reducing meal duration. A 15 residue fragment from the C-terminus of the CRF-like peptide, Locmi-DP(32-46), is fully active in the feeding assay, but has only weak ability to stimulate the accumulation of cAMP in tubules. Two smaller fragments, Locmi-DP(32-37) and Locmi-DP(41-46), were tested but neither had consistent biological activity in any of the assays used here. None of the peptides tested have any substantive activity in increasing cGMP in tubules.


Subject(s)
Corticotropin-Releasing Hormone/chemistry , Corticotropin-Releasing Hormone/pharmacology , Diuretics/chemical synthesis , Grasshoppers/chemistry , Insect Proteins/chemical synthesis , Insect Proteins/pharmacology , Amino Acid Sequence , Animals , Corticotropin-Releasing Hormone/analogs & derivatives , Corticotropin-Releasing Hormone/chemical synthesis , Diuretics/chemistry , Diuretics/pharmacology , Feeding Behavior/drug effects , In Vitro Techniques , Injections , Insect Proteins/chemistry , Malpighian Tubules/drug effects , Molecular Sequence Data , Peptide Fragments/chemical synthesis , Peptide Fragments/chemistry , Peptide Fragments/pharmacology
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