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1.
Bioorg Med Chem ; 27(1): 144-152, 2019 01 01.
Artículo en Inglés | MEDLINE | ID: mdl-30503411

RESUMEN

The γ-aminobutyric acid (GABA) transporter mGAT4 represents a promising drug target for the treatment of epilepsy and other neurological disorders; however, the lack of highly potent and selective inhibitors for mGAT4 still retards its pharmacological elucidation. Herein, the generation and screening of pseudostatic combinatorial hydrazone libraries at the murine GABA transporter mGAT4 for the search of novel GABA uptake inhibitors is described. The hydrazone libraries contained more than 1100 compounds derived from nipecotic acid derivatives substituted at the 5-position instead, as common, at the 1-position of the core structure. Two hits were found and evaluated, which display potencies in the lower micromolar range at mGAT4 and its human equivalent hGAT3. These compounds possess a lipophilic moiety derived from a biphenyl residue attached to the 5-position of the hydrophilic nipecotic acid moiety via a three-atom spacer. Thus, the novel structures with potencies close to that of the bench mark mGAT4 inhibitor (S)-SNAP-5114 add new insights into the structure-activity relationship of mGAT4 inhibitors and could provide a promising starting point for the development of new mGAT4 inhibitors with even higher potencies.


Asunto(s)
Proteínas Transportadoras de GABA en la Membrana Plasmática/metabolismo , Inhibidores de Recaptación de GABA/farmacología , Hidrazonas/farmacología , Ácidos Nipecóticos/farmacología , Bibliotecas de Moléculas Pequeñas/farmacología , Animales , Inhibidores de Recaptación de GABA/síntesis química , Inhibidores de Recaptación de GABA/química , Células HEK293 , Humanos , Hidrazonas/síntesis química , Hidrazonas/química , Ratones , Estructura Molecular , Ácidos Nipecóticos/síntesis química , Ácidos Nipecóticos/química , Bibliotecas de Moléculas Pequeñas/síntesis química , Bibliotecas de Moléculas Pequeñas/química , Relación Estructura-Actividad
2.
Toxicon ; 192: 74-77, 2021 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-33493497

RESUMEN

Despite the popularity of theraphosids, detailed reports on bite symptoms are still limited to few geographic regions and subfamilies. We therefore examined 363 published bite reports and noticed muscles cramps caused by theraphosids from nearly all continents and subfamilies. Symptoms are mostly locally restricted and mild, but 12.7% of victims experience pronounced cramps with highest incidence rates by Poecilotheriinae, Harpactirinae and Stromatopelminae subfamilies. We discuss how variations in venom quantity correlate with muscle cramp prevalence.


Asunto(s)
Picaduras de Arañas , Venenos de Araña , Arañas , Animales , Calambre Muscular/inducido químicamente , Espasmo/inducido químicamente
3.
Toxicon ; 190: 65-72, 2021 Jan 30.
Artículo en Inglés | MEDLINE | ID: mdl-33307110

RESUMEN

With a global estimate of tens of thousands of arachnid enthusiasts, spiders and scorpions are gaining increasing popularity as pets in industrialised countries in Europe, Northern America and Asia. As most spiders and all scorpions are venomous and due to their mostly negative image in the public media, several governments are already considering introducing legislation to regulate the domestic care of potentially dangerous captive animals. We aimed to investigate the circumstances and effects of exposure to arachnids kept in captivity. Thus, we collected and analysed data from 354 self-reported bites and stings attributed to pet arachnids. Our data revealed that on average there were less than 20 recorded envenomations per year with ~90% preventable by due care. We also categorized the severity of the resulting symptoms and found that the vast majority of symptoms were either local (60.7%) or minor (32.8%), 5.4% were asymptomatic, only 1.1% were severe and no fatalities were recorded. Based on our database of bite and sting reports, we performed a risk assessment for arachnid pet ownership and concluded that, with the proper care, arachnids can be safely kept as pets and pose a lower risk than many other recreational activities.


Asunto(s)
Venenos de Artrópodos , Mascotas , Picaduras de Escorpión/epidemiología , Picaduras de Arañas/epidemiología , Animales , Humanos
4.
ChemMedChem ; 14(5): 583-593, 2019 03 05.
Artículo en Inglés | MEDLINE | ID: mdl-30663849

RESUMEN

A screening of compound libraries based on nipecotic acid derivatives with lipophilic residues attached to the scarcely explored 5-position of the core structure was used for the search of new inhibitors of the γ-aminobutyric acid (GABA) transporter 1 (mGAT1). The generated compound libraries, which were based on hydrazone chemistry commonly used in dynamic combinatorial chemistry but rendered pseudostatic, were screened for their binding affinities toward mGAT1 by means of MS Binding Assays. With nipecotic acid derived hydrazone rac-16 h [rac-(3R,5S)-{5-[(E)-2-{[5-(2-phenylethynyl)thiophen-2-yl]methylidene}hydrazin-1-yl]piperidine-3-carboxylic acid}-sodium chloride (1/2)], one hit was found and evaluated displaying sub-micromolar potency (pKi =6.62±0.04) and a noncompetitive interaction mode at mGAT1. By bearing a 5-(2-phenylethynyl)thiophen-2-yl residue attached to the 5-position of nipecotic acid via a three-atom spacer, compound rac-16 h contains a structural moiety so far unprecedented for these kinds of bioactive molecules, and complements novel 5-substituted nipecotic acid derived ligands of mGAT1 revealed in a recently published screening campaign. This new class of ligands, with an inhibition mode distinct from that of benchmark mGAT1 inhibitors, could serve as research tools for investigations of mGAT1-mediated GABA transport.


Asunto(s)
Proteínas Transportadoras de GABA en la Membrana Plasmática/metabolismo , Inhibidores de Recaptación de GABA/química , Hidrazonas/química , Ácidos Nipecóticos/química , Bibliotecas de Moléculas Pequeñas/química , Espectrometría de Masa por Ionización de Electrospray/métodos , Unión Competitiva , Cromatografía Líquida de Alta Presión , Evaluación Preclínica de Medicamentos/métodos , Inhibidores de Recaptación de GABA/metabolismo , Células HEK293 , Humanos , Hidrazonas/metabolismo , Ligandos , Estructura Molecular , Bibliotecas de Moléculas Pequeñas/metabolismo , Relación Estructura-Actividad
5.
J Med Chem ; 61(22): 10310-10332, 2018 11 21.
Artículo en Inglés | MEDLINE | ID: mdl-30376325

RESUMEN

This study describes the screening of dynamic combinatorial libraries based on nipecotic acid as core structure with substituents attached to the 5- instead of the common 1-position for the search of novel inhibitors of the GABA transporter GAT1. The generated pseudostatic hydrazone libraries included a total of nearly 900 compounds and were screened for their binding affinities toward GAT1 in competitive mass spectrometry (MS) based Binding Assays. Characterization of the hydrazones with the highest affinities (with cis-configured rac-16gf bearing a 5-(1-naphthyl)furan-2-yl residue and a four atom spacer being the most potent) in binding and uptake experiments revealed an allosteric interaction at GAT1, which was not reported for any other nipecotic acid derivative up to now. Therefore, the herein introduced 5-substituted nipecotic acid derivatives could serve as valuable tools for investigations of allosterically modulated GABA transport mediated by GAT1 and furthermore as starting point for a new class of GAT1 inhibitors.


Asunto(s)
Proteínas Transportadoras de GABA en la Membrana Plasmática/metabolismo , Hidrazonas/química , Hidrazonas/metabolismo , Espectrometría de Masas , Aldehídos/química , Regulación Alostérica , Evaluación Preclínica de Medicamentos , Proteínas Transportadoras de GABA en la Membrana Plasmática/química , Humanos , Ligandos , Modelos Moleculares , Conformación Proteica
6.
Toxicon ; 138: 173-183, 2017 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-28866287

RESUMEN

The public perception of spiders and scorpions is skewed towards the potential harm they can inflict in humans, despite recent scientific evidence that arachnid venom components might be useful as bioinsecticides or even human therapeutics. Nevertheless, arachnids are becoming more popular as pets in Europe, America and Asia, raising the question for regulatory agencies in these regions as to whether they need to take measurements to protect their citizens. In order to decide upon the necessary regulatory steps, they first need to determine which arachnids are actually dangerous to humans. This review therefore provides an overview of the current literature on verified bites and stings from spiders and scorpions with the aim of assessing their potential danger for human health. As a guideline, we also provide a list of those arachnid genera that we consider as potentially dangerous, which includes 10 spider and 11 scorpion genera. The arachnid genera classified as dangerous comprise less than a quarter of all extant scorpion species and only 0.5% of all spiders species, with the actual number most likely being much lower than that, as not all species in those genera might turn out to pose an actual threat for humans. In conclusion, we found that only a small percentage of scorpions and a minute percentage of all spiders can be considered as potentially dangerous to humans. While in some countries of origin the high incidence of envenomations by dangerous arachnids can result in a serious problem to the health system, we assessed the risk that the same species pose when kept as pets under controlled maintenance conditions as significantly lower.


Asunto(s)
Picaduras de Escorpión , Picaduras de Arañas , Animales , Humanos , Mascotas , Venenos de Escorpión/toxicidad , Escorpiones/clasificación , Venenos de Araña/toxicidad , Arañas/química
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