The underlying physiological basis of the desert rodent Meriones shawi's survival to prolonged water deprivation: Central vasopressin regulation on peripheral kidney water channels AQPs-2

Acta Histochem. 2018 Feb;120(2):65-72. doi: 10.1016/j.acthis.2017.11.006. Epub 2017 Dec 6.

Abstract

Meriones shawi (M. shawi) is a particular semi-desert rodent known by its resistance to long periods of thirst. The aim of the present investigation is to clarify the underlying mechanisms allowing M. shawi to resist to hard conditions of dehydration. For this reason we used two different approaches: i) a morphometric study, which consists in measuring the effect of dehydration on body and kidneys weights as well as the report kidney weight/body weight, ii) By immunohistochemistry, we proceed to study the effect of dehydration on the immunoreactivity of central vasopressin (AVP) and the kidney aquaporin-2 (AQP-2) which is a channel protein that allows water to permeate across cell membranes. Our results showed both a body mass decrease accompanied by a remarkable kidneys hypertrophy. The immunohistochemical study showed a significant increase of AQP-2 immunoreactivity in the medullar part of Meriones kidneys allowing probably to Meriones a great ability to water retention. Consistently, we demonstrate that the increased AQP-2 expression occurred together with an increase in vasopressin (AVP) expression in both hypothalamic supraoptic (SON) and paraventricular nucleus (PVN), which are a major hub in the osmotic control circuitry. These various changes seen either in body weight and kidneys or at the cellular level might be the basis of peripheral control of body water homeostasis, providing to M. shawia strong resistance against chronic dehydration.

Keywords: AQP-2; Dehydration; Immunohistochemistry; Kidney; Meriones shawi.

MeSH terms

  • Animals
  • Aquaporin 2 / chemistry*
  • Aquaporin 2 / drug effects
  • Gerbillinae / physiology*
  • Immunohistochemistry
  • Kidney / drug effects
  • Kidney / physiology*
  • Male
  • Survival / physiology
  • Vasopressins / pharmacology
  • Vasopressins / physiology*
  • Water Deprivation*

Substances

  • Aquaporin 2
  • Vasopressins