Pharmacological characterization of a tyramine receptor from the southern cattle tick, Rhipicephalus (Boophilus) microplus

Insect Biochem Mol Biol. 2015 Aug:63:47-53. doi: 10.1016/j.ibmb.2015.04.008. Epub 2015 May 6.

Abstract

The southern cattle tick (Rhipicephalus (Boophilus) microplus) is a hematophagous external parasite that vectors the causative agents of bovine babesiosis or cattle tick fever, Babesia bovis and B. bigemina, and anaplasmosis, Anaplasma marginale. The southern cattle tick is a threat to the livestock industry in many locations throughout the world. Control methods include the use of chemical acaricides including amitraz, a formamidine insecticide, which is proposed to activate octopamine receptors. Previous studies have identified a putative octopamine receptor from the southern cattle tick in Australia and the Americas. Furthermore, this putative octopamine receptor could play a role in acaricide resistance to amitraz. Recently, sequence data indicated that this putative octopamine receptor is probably a type-1 tyramine receptor (TAR1). In this study, the putative TAR1 was heterologously expressed in Chinese hamster ovary (CHO-K1) cells, and the expressed receptor resulted in a 39-fold higher potency for tyramine compared to octopamine. Furthermore, the expressed receptor was strongly antagonized by yohimbine and cyproheptadine, and mildly antagonized by mianserin and phentolamine. Tolazoline and naphazoline had agonistic or modulatory activity against the expressed receptor, as did the amitraz metabolite, BTS-27271; however, this was only observed in the presence of tyramine. The southern cattle tick's tyramine receptor may serve as a target for the development of anti-parasitic compounds, in addition to being a likely target of formamidine insecticides.

Keywords: G-protein-coupled receptor; GPCR; Rhipicephalus microplus; Southern cattle tick; Tick; Tyramine receptor.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Acaricides / pharmacology
  • Amidines / pharmacology
  • Animals
  • CHO Cells
  • Cricetulus
  • Cyproheptadine / pharmacology
  • Octopamine / metabolism
  • Receptors, Biogenic Amine / antagonists & inhibitors
  • Receptors, Biogenic Amine / metabolism*
  • Rhipicephalus / metabolism*
  • Toluidines / pharmacology
  • Tyramine / metabolism*
  • Yohimbine / pharmacology

Substances

  • Acaricides
  • Amidines
  • Receptors, Biogenic Amine
  • Toluidines
  • norsynephrine receptor
  • tyramine receptor
  • Octopamine
  • Yohimbine
  • Cyproheptadine
  • U 40481
  • amitraz
  • Tyramine