Video Experimental Relacionado
Updated: Jun 21, 2026

11:01
Preparation and In Vivo Use of an Activity-based Probe for N-acylethanolamine Acid Amidase
Published on: November 23, 2016
Adenilato ciclasa sensible a la dopamina: ubicación en la sustancia negra
Resumen
Los receptores de dopamina en la sustancia negra de la rata no están en las células de dopamina. En cambio, se encuentran en vías que se proyectan desde el cerebro anterior, involucrando GABA o sustancia P.
Área de la Ciencia:
- La neurociencia es la neurociencia.
- La neuroquímica es la neuroquímica.
Sus antecedentes:
- La adenilato ciclasa sensible a la dopamina existe en la sustancia negra de la rata.
- Sus características se asemejan a las encontradas en el estriado.
Objetivo del estudio:
- Para determinar la ubicación de los receptores de dopamina en la sustancia negra.
- Investigar si estos receptores se encuentran en los cuerpos celulares de la dopamina o en vías asociadas.
Principales métodos:
- Estudios de lesiones en ratas.
- Aplicación intranigral de 6-hidroxidopamina para destruir los cuerpos celulares de la dopamina.
- Hemitransección cerebral y lesiones circunscritas de las vías estriatonigrales.
Principales resultados:
- La destrucción de los cuerpos celulares de dopamina no abolió el efecto de la dopamina en la adenilato ciclasa nigral.
- La lesión de las vías estriatonigrales abolió la estimulación de la dopamina de la adenilato ciclasa en la sustancia negra.
Conclusiones:
- Los receptores de dopamina en la sustancia negra no se encuentran en los cuerpos celulares de la dopamina.
- Estos receptores están asociados con vías aferentes, potencialmente involucrando GABA o sustancia P, que se proyectan desde el cerebro anterior.
Videos de Conceptos Relacionados
Enzyme-linked Receptors
Enzyme-linked receptors are proteins that act as both receptor and enzyme, activating multiple intracellular signals. This is a large group of receptors that include the receptor tyrosine kinase (RTK) family. Many growth factors and hormones bind to and activate the RTKs.
Neurotrophin (NT) receptors are a family of RTKs, including trkA, trkB, and trkC (tropomyosin-related kinase) receptors. TrkA is specific for nerve growth factor (NGF), neurotrophin-6, and neurotrophin-7. TrkB binds...
Neurotrophin (NT) receptors are a family of RTKs, including trkA, trkB, and trkC (tropomyosin-related kinase) receptors. TrkA is specific for nerve growth factor (NGF), neurotrophin-6, and neurotrophin-7. TrkB binds...
Enzyme Inhibition
Inhibitors are molecules that reduce enzyme activity by binding to the enzyme. In a normally functioning cell, enzymes are regulated by a variety of inhibitors. Drugs and other toxins can also inhibit enzymes. Some inhibitors bind to the enzyme’s active site, while others inhibit enzymatic activity by binding to other sites on the protein structure.
Multi-pass Transmembrane Proteins and β-barrels
In multi-pass transmembrane proteins, the polypeptide chain crosses the membrane more than once. The transmembrane polypeptide chain either forms an α-helix or β-strand structure. α-Helix containing multi-pass transmembrane proteins are ubiquitous, whereas β-strand containing ones are mainly found in gram-negative bacteria, mitochondria, and chloroplasts.
α-Helix containing multi-pass transmembrane proteins
Multi-pass transmembrane proteins such as G-protein-linked receptors (GPCRs) and...
α-Helix containing multi-pass transmembrane proteins
Multi-pass transmembrane proteins such as G-protein-linked receptors (GPCRs) and...
Transducer Mechanism: Enzyme-Linked Receptors
Enzyme-linked receptors are cell-surface receptors acting as an enzyme or associating with an enzyme intracellularly. They make excellent drug targets. Drugs can bind to the extracellular ligand-binding domain or directly affect their enzymatic domain and alter their activity.
Major types that are helpful drug targets include:
Major types that are helpful drug targets include:
Adrenergic Receptors: β Subtype
β-adrenoceptors have varied sensitivities towards adrenaline, noradrenaline, and isoprenaline. The order of agonist potency is as follows:
Isoprenaline > Adrenaline > Noradrenaline
Neurotransmitter binding to these receptors causes activation of adenylyl cyclase resulting in increased concentrations of cAMP and modulation of calcium ion channels within the cell. They are further classified into β1, β2, and β3 subtypes.
β1-adrenoceptors: β1-adrenoceptors have equal affinities for...
Isoprenaline > Adrenaline > Noradrenaline
Neurotransmitter binding to these receptors causes activation of adenylyl cyclase resulting in increased concentrations of cAMP and modulation of calcium ion channels within the cell. They are further classified into β1, β2, and β3 subtypes.
β1-adrenoceptors: β1-adrenoceptors have equal affinities for...
Antifungal Agents
Amphotericin B is a broad-spectrum antifungal agent that exploits structural differences between fungal and mammalian cell membranes. Its amphipathic structure—featuring a hydrophobic polyene-lactone ring and a hydrophilic region containing mycosamine and carboxylic acid groups—enables selective binding to ergosterol, a sterol predominantly found in fungal plasma membranes. This selective interaction underlies the drug’s antifungal activity, although weak binding to cholesterol contributes to...

