Effect of intracerebroventricular epinephrine microinjection on blood pressure and urinary sodium handling in gestational protein-restricted male adult rat offspring

Author(s)

Cardoso, Barbara Vaccari ; Custedio, Augusto Henrique ; Boer, Patricia Aline ; Rocha Gontijo, Jose Antonio ^[1]

Affiliation

^[1] Univ Estadual Campinas, Fetal Programming Lab, Nucleus Med & Expt Surg, Dept Internal Med, Fac Med Sci, BR-13083894 Campinas, SP - Brazil

• Document type: Journal article
• Source: BIOLOGY OPEN; v. 8, n. 4 APR 2019.
• Web of Science Citations: 0

Abstract

In this study, we hypothesized that blunting of the natriuresis response to intracerebroventricularly (ICV) microinjected adrenergic agonists is involved in the development of hypertension in maternal low-protein intake (LP) offspring. A stainless steel cannula was stereotaxically implanted into the right lateral ventricle (LV), then we evaluated the ICV administration of adrenergic agonists at increasing concentrations, and of alpha 1 and alpha 2-adrenoceptor antagonists on blood pressure and urinary sodium handling in LP offspring relative to an age-matched normal-protein intake (NP) group. We confirmed that epinephrine (Epi) microinjected into the LV of conscious NP rats leads to enhanced natriuresis followed by a reduction in arterial pressure. This response is associated with increased proximal and post-proximal sodium excretion accompanied by an unchanged glomerular filtration rate. The current study showed, in both NP and LP offspring, that the natriuretic effect of Epi injection into the LV was abolished by prior local microinjection of an alpha 1-adrenoceptor antagonist (prazosin). Conversely, LV alpha 2-adrenoceptor antagonist (yohimbine) administration potentiated the action of Epi. The LV yohimbine pretreatment normalized urinary sodium excretion and reduced the blood pressure in LP compared with age-matched NP offspring. These are, as far as we are aware, the first results showing the role of central adrenergic receptors' interaction on hypertension pathogenesis in maternal LP fetal-programming offspring. This study also provides good evidence for the existence of central nervous system adrenergic mechanisms consisting of alpha 1 and alpha 2-adrenoceptors, which work reciprocally on the control of renal sodium excretion and blood pressure. Although the precise mechanism of the different natriuretic response of NP and LP rats is still uncertain, these results lead us to speculate that inappropriate neural adrenergic pathways might have significant effects on tubule sodium transport, resulting in the inability of the kidneys to control hydrosaline balance and, consequently, an increase in blood pressure. (AU)

• FAPESP's process: 13/12486-5 - Fetal programming: on the kidney and neural ontogenesis
• Grantee: Jose Antonio Rocha Gontijo
• Support Opportunities: Regular Research Grants