Release of amino acids and related compounds from the adrenal equivalent and caudal vein of the eel in vitro

Author(s):  
L. Milakofsky ◽  
A. Epple ◽  
B. Nibbio ◽  
B. Gower ◽  
M.H. Stetson
1977 ◽  
Vol 32 (4) ◽  
pp. 447-452 ◽  
Author(s):  
Akila Said ◽  
Daisy Hanna Fleita ◽  
Hakim Grace Shinouda

A detailed investigation has been carried out on the effect of alloxan, alloxanic acid and ninhydrin on the rate of disappearance of alanine in buffered aqueous solution at pH 7 and on amino acids in blood both in vitro and in vivo. The results obtained indicate the possibility that the interaction of alloxan and tissue amino acids might have an important role in the diabetogenic effect of alloxan.


1964 ◽  
Vol 10 (2) ◽  
pp. 201-219 ◽  
Author(s):  
D. J. Royle ◽  
C. J. Hickman

Pythium aphanidermatum zoospores in distilled water suspension showed differential responses towards a range of single compounds, and mixtures, diffusing from the ends of capillary tubes containing these materials in agar. All substances caused an initial disorientation of zoospore movement followed, according to the substance under test, by indifference, repulsion, attraction, trapping, and encystment, or, at extreme pH, by loss of motility and death. Of a wide range of substances and mixtures tested, including sugars, amino acids, inorganic salts, organic acids, auxins, and vitamins, only glutamic acid, after weak base adjustment, and mixtures of sugars combined with mixtures of amino acids, induced the pattern of response observed with roots and root materials. Comparison of the activity of glutamate and structurally related compounds indicated that the effectiveness of glutamate was dependent on the presence of several moieties of the glutamate ion.Short photographic exposures allowed counts to be made of zoospores and cysts around the capillary mouth and provided a method for comparing, quantitatively, the accumulation of zoospores in response to different substances over a period of time.The substances inducing activity were readily detected in pea root exudate and extract and are, in fact, of general occurrence in roots. The effectiveness of the active principle(s) in root exudate and extract was roughly proportional to the concentration of these root materials in terms of their content of carbon and nitrogen but no such relation could be established for glutamic acid and a joint mixture of amino acids and sugars, suggesting the existence in root materials of additional factor(s).


2021 ◽  
Vol 95 ◽  
Author(s):  
Y. Mitsui ◽  
M. Miura ◽  
K. Kato ◽  
Y. Aoki

Abstract Since the exogenous compound tris(hydroxymethyl)aminomethane (Tris) showed a potent chemoattractant activity for Brugia pahangi infective third-stage larvae (L3), it was assumed that, in natural infection to a host, filarial L3 can be expected to recognize an endogenous Tris-related compound. In addition, a few amino acids have been identified as water-soluble attractants for second-stage juveniles of Meloidogyne incognita, a plant parasitic nematode. Therefore, the present study assesses the in vitro chemotactic responses of B. pahangi L3 to Tris-related compounds and amino acids using an agar-plate assay. Among Tris-related compounds, 2-amino-1,3-propanediol (APD) and 2-amino-2-methyl-1,3-propanediol (AMPD) exhibited a potent chemoattractant activity for filarial L3 at a level similar to Tris. Furthermore, arginine (Arg) was identified as a potent attractant for filarial L3 among amino acids. In addition, filarial L3 were attracted to Arg, APD and AMPD in mild alkaline conditions rather than acidic conditions. The chemoattractant activity of the three compounds for filarial L3 was observed in concentrations between 6.3 and 200 mm. This is the first report to demonstrate that Arg, APD and AMPD are potent chemoattractants for B. pahangi L3. Endogenous Arg and APD, in particular, may be involved in the regulation of the chemotactic behaviour of filarial L3 in the infection to a host. The present results will help to elucidate the mechanism of filarial skin-penetrating invasion of a host.


2003 ◽  
Vol 74 (4) ◽  
pp. 313-319 ◽  
Author(s):  
Rokibul Islam KHAN ◽  
Sada ANDO ◽  
Toshihiro TAKAHASHI ◽  
Tetsuo MORITA ◽  
Ryoji ONODERA

2019 ◽  
Vol 9 (1) ◽  
Author(s):  
D. Roeland Boer ◽  
Marie-José Bijlmakers

Abstract Novel strategies to target Trypanosoma brucei, Trypanosoma cruzi and Leishmania are urgently needed to generate better and safer drugs against Human African Trypanosomiasis, Chagas disease and Leishmaniasis, respectively. Here, we investigated the feasibility of selectively targeting in trypanosomatids the ubiquitin E1 activating enzyme (UBA1), an essential eukaryotic protein required for protein ubiquitination. Trypanosomatids contain two UBA1 genes in contrast to mammals and yeast that only have one, and using T. brucei as a model system, we show that both are active in vitro. Surprisingly, neither protein is inhibited by TAK-243, a potent inhibitor of human UBA1. This resistance stems from differences with the human protein at key amino acids, which includes a residue termed the gatekeeper because its mutation in E1s leads to resistance to TAK-243 and related compounds. Importantly, our results predict that trypanosomatid selective UBA1 inhibition is feasible and suggest ways to design novel compounds to achieve this.


2019 ◽  
Vol 19 (22) ◽  
pp. 1952-1961 ◽  
Author(s):  
J.C. Sobrinho ◽  
A.F. Francisco ◽  
R. Simões-Silva ◽  
A.M. Kayano ◽  
J.J. Alfonso Ruiz Diaz ◽  
...  

Background: Several studies have aimed to identify molecules that inhibit the toxic actions of snake venom phospholipases A2 (PLA2s). Studies carried out with PLA2 inhibitors (PLIs) have been shown to be efficient in this assignment. Objective: This work aimed to analyze the interaction of peptides derived from Bothrops atrox PLIγ (atPLIγ) with a PLA2 and to evaluate the ability of these peptides to reduce phospholipase and myotoxic activities. Methods: Peptides were subjected to molecular docking with a homologous Lys49 PLA2 from B. atrox venom modeled by homology. Phospholipase activity neutralization assay was performed with BthTX-II and different ratios of the peptides. A catalytically active and an inactive PLA2 were purified from the B. atrox venom and used together in the in vitro myotoxic activity neutralization experiments with the peptides. Results: The peptides interacted with amino acids near the PLA2 hydrophobic channel and the loop that would be bound to calcium in Asp49 PLA2. They were able to reduce phospholipase activity and peptides DFCHNV and ATHEE reached the highest reduction levels, being these two peptides the best that also interacted in the in silico experiments. The peptides reduced the myotubes cell damage with a highlight for the DFCHNV peptide, which reduced by about 65%. It has been suggested that myotoxic activity reduction is related to the sites occupied in the PLA2 structure, which could corroborate the results observed in molecular docking. Conclusion: This study should contribute to the investigation of the potential of PLIs to inhibit the toxic effects of PLA2s.


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