Development and characterization of a highly selective neuropeptide Y Y5 receptor agonist radioligand: [125I][hPP1-17, Ala31, Aib32]NPY

Abstract

(1) The existence of multiple classes of neuropeptide Y (NPY) receptors (Y(1), Y(2), Y(4), Y(5) and y(6)) is now well established. However, one of the major difficulties in the study of these various receptor subtypes is the current lack of highly selective probes to investigate a single receptor class. Up to most recently, this was particularly true for the Y(4) and Y(5) subtypes. (2) [hPP(1-17), Ala(31), Aib(32)]NPY, the first highly selective Y(5) agonist, was iodinated using the chloramine T method and purified by high-pressure liquid chromatography. (3) Binding performed in rat brain homogenates revealed that equilibrium was reached after 120 min (t(1/2)=21 min) and 60 min (t(1/2)=12 min) at 25 and 100 pM [(125)I][hPP(1-17), Ala(31), Aib(32)]NPY, respectively. (4) Isotherm saturation binding experiments demonstrated that [(125)I][hPP(1-17), Ala(31), Aib(32)]NPY binds to an apparent single population with high-affinity (K(D) of 1.2 and 1.7 nM) and low-capacity (B(max) of 14+/-3 fmol/100,000 cells and 20+/-5 fmol/mg protein) sites in Y(5) receptor HEK293-transfected cells and rat brain membrane homogenates, respectively. No specific [(125)I][hPP(1-17), Ala(31), Aib(32)]NPY binding sites could be detected in Y(1), Y(2) or Y(4) receptors transfected HEK293 cells, demonstrating the high selectivity of this ligand for the Y(5) subtype. (5) Competition binding experiments performed in rat brain membrane homogenates and Y(5)-receptor transfected HEK293 cells demonstrated that specific [(125)I][hPP(1-17), Ala(31), Aib(32)]NPY binding was competed with high affinity by Y(5) agonists and antagonists such as [Ala(31), Aib(32)]NPY, [hPP(1-17), Ala(31), Aib(32)]NPY, hPP, CGP71683A and JCF109, but not by Y(1) (BIBP3226), Y(2) (BIIE0246) and Y(1)/Y(4) (GR231118) preferential ligands. (6) Taken together, these data demonstrate that [(125)I][hPP(1-17), Ala(31), Aib(32)]NPY is the first highly selective Y(5) radioligand to be developed. This new probe should prove most useful for further detailed studies of the molecular and pharmacological properties of this receptor subtype in brain and peripheral tissues.

Figure 1

Typical HPLC purification profile of radiolabelled [¹²⁵I][Ala³¹, Aib³²]NPY (a) and [¹²⁵I][hPP_1–17, Ala³¹, Aib³²]NPY (b).

Figure 2

Typical profiles of the time course association of [¹²⁵I][hPP_1–17, Ala³¹, Aib³²]NPY binding in rat brain membrane homogenates at room temperature. Data represent the mean±s.e.m. of a prototypical experiment performed in triplicate.

Figure 3

Typical profiles of saturation binding isotherms of [¹²⁵I][hPP_1–17, Ala³¹, Aib³²]NPY binding in HEK293 cells transfected with the rat Y₅ receptor cDNA (a) and rat brain membrane homogenates (b). Inset is a Scatchard transformation of the isotherm saturation binding experiment. Data represent the mean±s.e.m. of a prototypical experiment performed in triplicate.

Figure 4

Competition binding profiles of various agonists and antagonists of the NPY family against specific [¹²⁵I][hPP_1–17, Ala³¹, Aib³²]NPY binding in HEK293 cells transfected with the rat Y₅ receptor cDNA (a) and rat brain membrane homogenates (b). Data represent the mean±s.e.m. of three to six determinations, each performed in triplicate.

Figure 5

Comparative affinities of various analogues of the NPY family to compete against [¹²⁵I][hPP_1–17, Ala³¹, Aib³²]NPY in HEK293 cells transfected with the rat Y₅ receptor cDNA and rat brain membrane homogenates.