Abstract
Aquaporins (AQPs) are integral membrane proteins that serve as selective pores through which water and small solutes cross the plasma membranes of many human tissue and cell types. They have been identified in epithelia and endothelia involved in fluid transport, such as kidney tubules and glandular epithelia, glial cells, epidermis, and adipocytes. The pathophysiological roles of these proteins and the primary and secondary involvement of AQPs are becoming apparent in diverse clinical disorders, from diabetes insipidus to various forms of edema. The advanced understanding of aquaporin biology, from the structural determinants of channel permeability to the assignment of their physiological function in different organs, will allow the use of AQPs as targets for the therapy of a wide array of diseases. In this review, the mode of action of clinically-effective plant formulae on human AQPs-related diseases at the molecular, cellular, and organism levels is explored. The use of pharmacological plant-derived compounds as a possible strategy in the therapy of diseases related to altered water homeostasis should stimulate debate and further research objectives.
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Acknowledgments
This work was funded by projects of the CICYT (AGL2012-40175-C02-01). M.C. Martínez-Ballesta thanks the Spanish Ministerio de Ciencia e Innovación for funding through the “Ramón y Cajal” programme [Ref RYC-2009-04574]. The authors thank Dr. D. Walker for correction of the written English in the manuscript.
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del Carmen Martínez-Ballesta, M., Bou, G. & Carvajal, M. Aquaporins as targets of pharmacological plant-derived compounds. Phytochem Rev 13, 573–586 (2014). https://doi.org/10.1007/s11101-013-9314-4
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DOI: https://doi.org/10.1007/s11101-013-9314-4