Amiloride-sensitive Na⁺ absorption is a well-described feature of numerous transporting epithelia in vertebrates. Yet, very little is known about this important physiological process regarding invertebrates. In the present paper we compare vertebrate Na⁺ absorption mediated by the amiloride-sensitive epithelial Na⁺ channel (ENaC) and its invertebrate counterpart. We used the dorsal skin of the annelid Hirudo medicinalis as a model for the Na⁺ absorption of invertebrate epithelia. Applying electrophysiological, molecular, and biochemical techniques we found striking functional and structural differences between vertebrate and invertebrate amiloride-sensitive Na⁺ absorption. In modified Ussing chambers we analyzed the influence of different known blockers and effectors of vertebrate ENaC on leech epithelial Na⁺ absorption. We demonstrate that the serine protease trypsin had no effect on the Na⁺ transport across leech integument, while it strongly activates vertebrate ENaC. While protons, and the divalent cations Ni²⁺ and Zn²⁺ stimulate vertebrate ENaC, amiloride-sensitive Na⁺ currents in leech integument were substantially reduced. For molecular studies we constructed a cDNA library of Hirudo medicinalis and screened it with specific ENaC antibodies. We performed numerous PCR approaches using a vast number of different degenerated and specific ENaC primers to identify ENaC-like structures. Yet, both strategies did not reveal any ENaC-like sequence in leech integument. From these data we conclude that amiloride-sensitive Na⁺ absorption in leech skin is not mediated by an ENaC-like Na⁺ channel but by a still unknown invertebrate member of the ENaC/DEG family that we termed lENaTP (leech epithelial Na⁺ transporting protein).