Abstract

In fish, the intestine is fundamental for digestion, nutrient absorption, and other functions like osmoregulation, acid-base balance, and excretion of some metabolic products. These functions require a large exchange surface area, which, in turn, favors the absorption of natural and anthropogenic foreign substances (xenobiotics) either dissolved in water or contained in the food. According to their chemical nature, nutrients, ions, and water may cross the intestine epithelium cells’ apical and basolateral membranes by passive diffusion or through a wide array of transport proteins and also through endocytosis and exocytosis. In the same way, xenobiotics can cross this barrier by passive diffusion or taking advantage of proteins that transport physiological substrates. The entry of toxic substances is counterbalanced by an active efflux transport mediated by diverse membrane proteins, including the ATP binding cassette (ABC) proteins. Recent advances in structure, molecular properties, and functional studies have shed light on the importance of these proteins in cellular and organismal homeostasis. There is abundant literature on mammalian ABC proteins, while the studies on ABC functions in fish have mainly focused on the liver and, to a minor degree, on the kidney and other organs. Despite their critical importance in normal physiology and as a barrier to prevent xenobiotics incorporation, fish intestine’s ABC transporters have received much less attention. All the ABC subfamilies are present in the fish intestine, although their functionality is still scarcely studied. For example, there are few studies of ABC-mediated transport made with polarized intestinal preparations. Thus, only a few works discriminate apical from basolateral transport activity. We briefly describe the main functions of each ABC subfamily reported for mammals and other fish organs to help understand their roles in the fish intestine. Our study considers immunohistochemical, histological, biochemical, molecular, physiological, and toxicological aspects of fish intestinal ABC proteins. We focus on the most extensively studied fish ABC proteins (subfamilies ABCB, ABCC, and ABCG), considering their apical or basolateral location and distribution along the intestine. We also discuss the implication of fish intestinal ABC proteins in the transport of physiological substrates and aquatic pollutants, such as pesticides, cyanotoxins, metals, hydrocarbons, and pharmaceutical products.

Highlights

  • Aquatic animals take up food and water together; their digestive systems are exposed to xenobiotics present in the food or dissolved in water

  • The whole-genome analyses presented in the previous section of this review show that at least one of these transporters is present in any genome

  • HR cells accumulate several fluorescent ATP binding cassette (ABC) substrates but not rhodamine B, and the addition of ABCB1 and ABCC inhibitors significantly increase this accumulation. These results suggest a protective role of the epidermis ionocytes in part through Abcb5-mediated efflux of toxic molecules in early stages with not completely developed detoxification organs

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Summary

Introduction

Aquatic animals take up food and water together; their digestive systems are exposed to xenobiotics present in the food or dissolved in water. This risk is enhanced in marine teleost fish, which drink high volumes of water for osmoregulation purposes. The intestinal epithelium (mucosa) is the main surface of alkaline digestion and nutrient absorption and reabsorption of bile acids. These functions require a large surface area of epithelial tissue with a broad spectrum of inwardly directed membrane transporters. The parent or biotransformed substance is transported by the blood to the liver and the kidney to be metabolized and excreted (Wang and Wang, 2016)

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