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Membrane permeability is fundamental to all cell biology and
subcellular biology. The cell exists as a closed unit. Import and
export depend upon a number of sophisticated mechanisms, such as
active transport, endocytosis, exocytosis, and passive diffusion.
These systems are critical for the normal housekeeping
physiological functions. However, access to the cell is also taken
advantage of by toxic microbes (such as cholera or ptomaine) and
when designing drugs.
Sodium reabsorbing epithelia play a major role in whole-body sodium
homeostasis. Some examples of sodium regulating tissues include
kidney, colon, lung, and sweat ducts. Sodium transport across these
membranes is a two-step process: entry through an
amiloride-sensitive sodium channel and exit via the
ouabain-sensitive sodium/potassium ATPase. The sodium entry
channels are the rate-limiting determinant for transport and are
regulated by several different hormones. The sodium channels also
play a significant role in a number of disease states, like
hypertension, edema, drug-induced hyperkalemia, and cystic
fibrosis. Amiloride-Sensitive Sodium Channels: Physiology and
Functional Diversity provides the first in-depth exchange of ideas
concerning these sodium channels, their regulation and involvement
in normal and pathophysiological situations.
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