Canales de calcio como blanco de interés farmacológico

Yenny Yolanda Lozano Jiménez; Ruth Mélida Sánchez Mora

doi:10.22490/24629448.3926

Vol. 18 No. 34 (2020)

Published 2020-07-09

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Article of Review (before OJS)

Calcium channels as a pharmacological target

DOI: https://doi.org/10.22490/24629448.3926

Yenny Yolanda Lozano Jiménez

Ruth Mélida Sánchez Mora

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Abstract
References

Calcium channels are membrane proteins that constitute the most important route for the entry of the calcium ion (Ca²⁺) into the cell. When opened, they allow selective ion entrance, starting a variety of processes such as muscular contraction, endocrine secretion and neurotransmitters release, among others. These proteins are classified in three categories according to their structural and functional properties: (i) Receptor-operated calcium channels (ROCC), (ii) Channels activated by physical parameters (Transient Receptor Potential or TRP-channels) and (iii) Voltage-dependent calcium channels (VDCCs), the latter being the most studied due to its presence in excitable cells. Given the importance of Ca²⁺ in the cellular physiology, the calcium channels constitute targets for pharmacological action for multiple treatments, and therefore, they are object of study for the development of new medicaments. The objective of this review is to explain the importance of the channels of Ca^{2 +} from a pharmacological projection, by exploring the articles published, bearing in mind topics related to the structure of the channels Ca²⁺, properties of their biophysics, cellular location, functioning and their pharmacological interaction.

keywords: Voltage, Depolarization, Potential, Ion Channel, Calcium Channel, Calcium Channel Blockers

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Lozano Jiménez, Y. Y., & Sánchez Mora , R. M. (2020). Calcium channels as a pharmacological target. NOVA Biomedical Sciences Journal, 18(34), 57-76. https://doi.org/10.22490/24629448.3926

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Calcium channels as a pharmacological target

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