Influence of thyroid state on cardiac and renal capillary density and glomerular morphology in rats
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2013Referencia bibliográfica
Rodriguez-Gomez, I., Banegas, I., Wangensteen, R., Quesada, A., Jiménez, R., Gómez-Morales, M., ... & Vargas, F. (2013). Influence of thyroid state on cardiac and renal capillary density and glomerular morphology in rats. Journal of Endocrinology, 216(1), 43-51.
Resumen
The purpose was to analyse the cardiac and renal capillary density and glomerular
morphology resulting from a chronic excess or deficiency of thyroid hormones (THs) in rats.
Weperformed histopathological, morphometrical and immunohistochemical analyses in
hypothyroid and hyperthyroid rats to evaluate the density of mesenteric, renal and cardiac
vessels at 4 weeks after induction of thyroid disorders. The main angiogenic factors in
plasma, heart and kidney were measured as possible mediators of vascular changes.
Mesenteric vessel branching was augmented and decreased in hyper- and hypothyroid rats
respectively. The numerical density of CD31-positive capillaries was higher in left and right
ventricles and in cortical and medullary kidney from both hyper- and hypothyroid rats vs
controls. Numbers of podocytes and glomeruli per square millimetre were similar among
groups. Glomerular area and percentage mesangium were greater in the hyperthyroid vs
control or hypothyroid groups. No morphological renal lesions were observed in any group.
Vascularisation of the mesenteric bed is related to TH levels, but an increased capillarity was
observed in heart and kidney in both thyroid disorders. This increase may be produced by
higher tissue levels of angiogenic factors in hypothyroid rats, whereas haemodynamic
factors would predominate in hyperthyroid rats. Our results also indicate that the renal
dysfunctions of thyroid disorders are not related to cortical or medullary microvascular
rarefaction and that the proteinuria of hyperthyroidism is not secondary to a podocyte
deficit. Finally, TH or its analogues may be useful to increase capillarity in renal diseases
associated with microvascular rarefaction





