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1.
J Biol Chem ; 270(4): 1575-82, 1995 Jan 27.
Artigo em Inglês | MEDLINE | ID: mdl-7829487

RESUMO

Purification of a material immunoreactive to an antiserum against angiotensin II and present in the central nervous system of the pharyngobdellid leech Erpobdella octoculata was performed by reversed-phase high pressure liquid chromatography combined with both enzyme-linked immunosorbent assay and dot immunobinding assays for angiotensin II. Establishment of the amino acid sequence by Edman degradation, electrospray, and fast atom bombardement mass spectrometry measurements and enzymatic treatment by carboxypeptidase A indicated that this "central" angiotensin II-like material, the first one fully characterized in the animal kingdom, is an angiotensin II amide. This finding constitutes also the first biochemical characterization of a peptide of the angiotensin family in an invertebrate. Synthetic angiotensin II amide exerts, when injected in leeches, a diuretic effect and is, 1 and 2 h postinjection, 100-fold more potent than vertebrate angiotensin II. An identification of the proteins immunoreactive to an antiserum against angiotensin II performed at the level of both central nervous system extracts and in vitro central nervous system-translated RNA products indicated that in the two cases, two proteins were detected. Their molecular masses, which were, respectively, approximately 14 and approximately 18 kDa for the central nervous system extracts and approximately 15 and approximately 19 kDa for in vitro central nervous system-translated RNA products, differ from that of angiotensinogen (approximately 60 kDa), the precursor of vertebrate angiotensin II.


Assuntos
Angiotensina II/análogos & derivados , Diuréticos/isolamento & purificação , Sanguessugas , Proteínas do Tecido Nervoso/química , Proteínas do Tecido Nervoso/isolamento & purificação , Sistema Nervoso/química , Sequência de Aminoácidos , Angiotensina II/química , Angiotensina II/isolamento & purificação , Angiotensina II/farmacologia , Animais , Cromatografia Líquida de Alta Pressão , Ensaio de Imunoadsorção Enzimática , Soros Imunes , Immunoblotting , Sanguessugas/efeitos dos fármacos , Dados de Sequência Molecular , Peso Molecular , Proteínas do Tecido Nervoso/farmacologia , Espectrometria de Massas de Bombardeamento Rápido de Átomos
2.
FEBS Lett ; 348(1): 102-6, 1994 Jul 04.
Artigo em Inglês | MEDLINE | ID: mdl-8026574

RESUMO

This paper reports the purification of a novel pro-opiomelanocortin derivative peptide (a gamma-melanocyte stimulating hormone-like (gamma-MSH-like) molecule) from the brain of the leech Theromyzon tessulatum. After reverse-phase HPLC purification, the sequence of the gamma-MSH-like peptide (YVMGHFRWDKFamide) was established by a combination of automated Edman degradation, electrospray mass spectrometry measurement, enzymatic treatment and co-elution experiments in reverse-phase HPLC with synthetic peptides.


Assuntos
Química Encefálica , Hormônios Estimuladores de Melanócitos/isolamento & purificação , Sequência de Aminoácidos , Animais , Humanos , Sanguessugas , Hormônios Estimuladores de Melanócitos/química , Hormônios Estimuladores de Melanócitos/fisiologia , Dados de Sequência Molecular , Peptídeos/química , Peptídeos/isolamento & purificação , Peptídeos/fisiologia , Homologia de Sequência de Aminoácidos
3.
Eur J Biochem ; 221(1): 269-75, 1994 Apr 01.
Artigo em Inglês | MEDLINE | ID: mdl-8168516

RESUMO

Using enzyme-linked immunosorbent assays, a dot-immunobinding assay and a three-step reverse-phase HPLC separation, four Arg-Phe-amide (RFamide) peptides were purified from sex segmental ganglia extracts of the leech Erpobdella octoculata; FMRFamide, FM(O)RFamide, FLRFamide and GDPFLRFamide. Their amino acid sequences were elucidated by means of a combined approach using antiserum specificity, synthetic-peptide coelution, automated Edman degradation and electrospray mass spectrometry. One of these peptides, GDPFLRFamide, is a novel leech RFamide neuropeptide. Two of the above RFamide peptides are involved in the control of leech hydric balance; one (GDPFLRFamide) is diuretic, the other (FMRFamide) is anti-diuretic. Titration of each purified RFamide peptide indicated a similar amount of each tetrapeptide and of tetrapeptides and heptapeptides. A comparison between RFamide peptides of E. octoculata and molluscs reveals structural similarities supporting the hypothesis for the existence of an ancestral RFamide peptide gene common to leeches and molluscs.


Assuntos
Sanguessugas/química , Neuropeptídeos/isolamento & purificação , Sequência de Aminoácidos , Animais , Cromatografia Líquida de Alta Pressão , Gânglios dos Invertebrados/química , Sanguessugas/fisiologia , Dados de Sequência Molecular , Neuropeptídeos/química , Neuropeptídeos/fisiologia , Análise de Sequência , Equilíbrio Hidroeletrolítico/fisiologia
4.
Brain Res ; 631(2): 247-55, 1993 Dec 24.
Artigo em Inglês | MEDLINE | ID: mdl-7510576

RESUMO

The peptides contained in neurons localized in the brain of the leech Theromyzon tessulatum (Hirudinae, Rhynchobdellida) and showing an immunopositive reaction with an antibody directed against angiotensin II (AII), were purified by reversed-phase HPLC. Three AII-like peptides (P1, P2 and P3) which exhibited the same retention times and chromatographic behaviors as synthetic AVII (fragment 6-8 of AII), AIV (fragment 3-8 of AII) and AII, respectively, were resolved in brain extracts. An identification of the proteins immunoreactive to an anti-AII was performed at the level of both brain extracts and in vitro brain-translated RNA products. The protein detected at the level of the brain extracts (of a molecular mass of approximately 18 kDa) is multipeptidic as it is also recognized by two other antisera, a polyclonal one directed against gamma-MSH and a monoclonal one (Tt159) raised against a leech brain epitope. It could be the pro-AII-like precursor. The protein detected at the level of in vitro brain-translated RNA products (of a molecular mass of approximately 19 kDa) could be the prepro-AII-like precursor.


Assuntos
Angiotensina II/metabolismo , Química Encefálica/fisiologia , Sanguessugas/metabolismo , Angiotensina II/imunologia , Animais , Anticorpos Monoclonais , Cromatografia Líquida de Alta Pressão , Eletroforese em Gel de Poliacrilamida , Ensaio de Imunoadsorção Enzimática , Immunoblotting , Proteínas do Tecido Nervoso/análise , Fragmentos de Peptídeos/análise , Peptídeos/análise , RNA/análise
5.
Comp Biochem Physiol Comp Physiol ; 104(1): 75-81, 1993 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-7679619

RESUMO

1. Using direct, inhibiting and competitive enzyme-linked immunosorbent assay (ELISA), two steps were involved in the mapping of the recognition site of a polyclonal antibody against oxytocin (OT). 2. The percentage of cross-reactivity between OT and the N-terminal or the C-terminal fragment of OT demonstrated that the C-terminal fragment is the antigenic part of OT. 3. The percentage of cross-reactivity between OT and other molecules of the OT family indicated that the amino acid in the 8-position and the C-terminal amide of the OT molecule contribute to the recognition. 4. In the two sex segmental ganglia of the leech Erpobdella octoculata, where cells immunoreactive to the anti-OT are detected, the antibody has allowed to characterize an epitope close to the mammalian OT by its C-terminal part.


Assuntos
Anticorpos/química , Epitopos/química , Sanguessugas/química , Neuropeptídeos/química , Ocitocina/química , Ocitocina/imunologia , Sequência de Aminoácidos , Animais , Formação de Anticorpos , Ligação Competitiva , Ensaio de Imunoadsorção Enzimática , Epitopos/imunologia , Gânglios/química , Gânglios/imunologia , Gônadas/inervação , Indicadores e Reagentes , Sanguessugas/anatomia & histologia , Dados de Sequência Molecular , Neuropeptídeos/imunologia , Mapeamento de Peptídeos , Titulometria
6.
Brain Res ; 601(1-2): 173-84, 1993 Jan 22.
Artigo em Inglês | MEDLINE | ID: mdl-7679306

RESUMO

A large number of oxytocin (OT)-like neurons were detected in the sex segmental ganglia (SG5, SG6) of three species of leeches belonging to different orders: Theromyzon tessulatum, Hirudo medicinalis and Erpobdella octoculata. In this latter species, an epitope close to the vertebrate OT by its C-terminal part (MSH release inhibiting factor: MIF), localized in granules of a size diameter of ca 120 nm and colocalized with FMRFamide(FMRFa)-like material was demonstrated. With reverse phase-high performance liquid chromatography, evidence was given that the two epitopes (OT and FMRFa) colocalized in the same neurons were biochemically different. A titration of OT per SG indicated that the OT-like amount was considerably higher in sex SG than in non-sex SG (ca. 5 pmol vs. ca. 0.5 pmol). Moreover, at the level of sex SG, this amount was ca. 3-fold higher in immature leeches than in mature specimens. Injections of extracts of SG of E. octoculata and of fragments of OT (Tocinoic acid or MIF) to T. tessulatum, indicated that MIF (the epitope found in the sex SG) and sex SG have the same anti-diuretic effect on the leeches injected. These results pointed to an anti-diuretic role of the leech OT-like substance.


Assuntos
Diurese/fisiologia , Epitopos/imunologia , Sanguessugas/metabolismo , Neurônios/metabolismo , Neuropeptídeos/fisiologia , Neurotransmissores/fisiologia , Ocitocina/fisiologia , Animais , Peso Corporal/efeitos dos fármacos , Cromatografia Líquida de Alta Pressão , Ensaio de Imunoadsorção Enzimática , FMRFamida , Feminino , Imunofluorescência , Gânglios/citologia , Gânglios/metabolismo , Gânglios/fisiologia , Imuno-Histoquímica , Hormônio Inibidor da Liberação de MSH/farmacologia , Masculino , Neuropeptídeos/imunologia , Neurotransmissores/imunologia , Oxirredução , Ocitocina/análogos & derivados , Ocitocina/imunologia , Ocitocina/farmacologia , Radioimunoensaio , Extratos de Tecidos/farmacologia
7.
Artigo em Inglês | MEDLINE | ID: mdl-1347734

RESUMO

1. Cells in the central nervous system of the leech Theromyzon tessulatum were revealed with an antiserum against angiotensin II. Among these cells, a group of 4-5 pairs of neurons, called beta giant cells, and located in the posterior compartments of the supraesophageal ganglion was particularly investigated. 2. The amount of angiotensin II-like substance(s) in the brain increased notably in the days immediately following the third meal. 3. Injections of angiotensin II, fragments 1-4 or 5-8 or angiotensin II and of angiotensin III into stage 3 leeches showed that fragment 5-8 of angiotensin II was the most effective: it provokes a loss of mass of the leeches, which could express a diuretic effect.


Assuntos
Angiotensina II/análise , Sistema Nervoso Central/química , Diurese/fisiologia , Angiotensina II/síntese química , Angiotensina II/fisiologia , Animais , Sistema Nervoso Central/ultraestrutura , Ensaio de Imunoadsorção Enzimática , Imuno-Histoquímica , Sanguessugas , Microscopia Eletrônica , Equilíbrio Hidroeletrolítico/fisiologia
8.
C R Acad Sci III ; 305(10): 411-5, 1987.
Artigo em Francês | MEDLINE | ID: mdl-3119164

RESUMO

Two mouse hybridomas producing monoclonal antibodies Tt9 and Tt 159 directed against antigens of supraesophageal ganglia of the leech T. tessulatum were selected to study the neuroendocrine control of osmoregulation in this species. One, Tt 159 reacted with an antigenic determinant of cells recognized by an anti-angiotensin antibody, the other, Tt 9, with neurons immunoreactive to the anti-vasopressin.


Assuntos
Anticorpos Monoclonais , Sanguessugas/citologia , Sanguessugas/fisiologia , Neurônios/citologia , Angiotensina II/imunologia , Animais , Sistema Nervoso Central/citologia , Neurônios/imunologia , Neuropeptídeos/análise , Vasopressinas/imunologia , Equilíbrio Hidroeletrolítico
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