St. Louis Encephalitis

Naranjo, Steven E.; Habeck, Dale; Asaro, Christopher; Boevé, Jean‐Luc; Baumgärtner, Johann; Schneider, David C.; Lambdin, Paris; Cave, Ronald D.; Ratcliffe, Brett C.; Scherer, Clay W.; Frank, J. Howard; Dunford, James C.; Somma, Louis A.; Richman, David B.; Krafsur, E. S.; Crooker, Allen; Menalled, Fabián D.; Liebman, Matt; Teal, Peter E. A.; Lloyd, James E.; Sivinski, John; Cranshaw, Whitney; Adler, Peter H.; Tsai, James H.; Zaspel, Jennifer M.; Liburd, Oscar E.; Sarzynski, Erin M.; Ellis, Jamie; Ellis, Amanda; Headings, Mark; Scotti, Paul D.; Christian, Peter D.; Stange, Lionel; Baldwin, Rebecca W.; Meer, Robert Κ. Vander; Preston, Catherine A.; Otis, Gard W.; Noling, Joseph W.; Bouicas, Drion G.; Sanborn, Allen; Ragsdale, David W.; Rossi, Anthony; Branham, Marc; Sourakov, Andrei; Amalin, Divina; Cushing, Paula E.; Clercq, Patrick De; Peck, Daniel C.; Thompson, Vinton; Bowles, David E.; Nealis, Vincent G.; Cilek, James E.; Klassen, Waldemar; Tilgner, Erich; Costas, Miguel; Vázquez, Ángeles; Panizzi, Antônio R.; Rey, Jorge R.; Kondratieff, Boris C.; Haunerland, Norbert H.; Hahn, Daniel A.; Lord, Jeffrey C.; Kathirithamby, Jeyaraney; Showler, Allan T.; Scheffrahn, Rufolf H.; Meagher, Robert L.; Gallo, Maria; Hunter, Fiona F.; Heppner, John B.; Gerling, Dan; Jolivet, Pierre; Capinera, John L.; Moriya, Seiichi; Hoy, Marjorie A.; Hou, Roger F.; Lawrence, Pauline O.; Burden, Beverly; Zhu, Kun Yan; Hangay, George

doi:10.1007/978-1-4020-6359-6_4409

Cited by 1 publication

(1 citation statement)

References 0 publications

Supporting

Mentioning

Contrasting

Order By: Relevance

“…During Ca 2+ -driven action potentials, large-conductance Ca 2+ -activated K + (BK) channels and voltage-dependent K + channels (K V 2.1/5.1) are responsible for repolarization and afterhyperpolarization (Heppner et al 1997; Thorneloe & Nelson, 2003;Herrera & Nelson, 2004). Activation of ATP-sensitive K + (K ATP ) channels causes membrane potential hyperpolarization, which decreases action potential frequency (Heppner et al 1996;Petkov et al 2001). K + channel-opening drugs, particularly those that activate K ATP and BK channels, have been explored as therapeutic agents to treat overactive bladder by decreasing UBSM excitability (Gopalakrishnan & Shieh, 2004).…”

Section: Introductionmentioning

confidence: 99%

The K_V7 channel activator retigabine suppresses mouse urinary bladder afferent nerve activity without affecting detrusor smooth muscle K⁺ channel currents

Tykocki

Heppner

Dalsgaard³

et al. 2018

The Journal of Physiology

View full text Add to dashboard Cite

Key points KV7 channels are a family of voltage‐dependent K+ channels expressed in many cell types, which open in response to membrane depolarization to regulate cell excitability. Drugs that target KV7 channels are used clinically to treat epilepsy. Interestingly, these drugs also cause urinary retention, but it was unclear how. In this study, we focused on two possible mechanisms by which retigabine could cause urinary retention: by decreasing smooth muscle excitability, or by decreasing sensory nerve outflow. Urinary bladder smooth muscle had no measurable KV7 channel currents. However, the KV7 channel agonist retigabine nearly abolished sensory nerve outflow from the urinary bladder during bladder filling. We conclude that KV7 channel activation likely affects urinary bladder function by blocking afferent nerve outflow to the brain, which is key to sensing bladder fullness. Abstract KV7 channels are voltage‐dependent K+ channels that open in response to membrane depolarization to regulate cell excitability. KV7 activators, such as retigabine, were used to treat epilepsy but caused urinary retention. Using electrophysiological recordings from freshly isolated mouse urinary bladder smooth muscle (UBSM) cells, isometric contractility of bladder strips, and ex vivo measurements of bladder afferent activity, we explored the role of KV7 channels as regulators of murine urinary bladder function. The KV7 activator retigabine (10 μM) had no effect on voltage‐dependent K+ currents or resting membrane potential of UBSM cells, suggesting that these cells lacked retigabine‐sensitive KV7 channels. The KV7 inhibitor XE‐991 (10 μM) inhibited UBSM K+ currents; the properties of these currents, however, were typical of KV2 channels and not KV7 channels. Retigabine inhibited voltage‐dependent Ca2+ channel (VDCC) currents and reduced steady‐state contractions to 60 mM KCl in bladder strips, suggesting that reduction in VDCC current was sufficient to directly affect UBSM function. To determine if retigabine altered ex vivo bladder sensory outflow, we measured afferent activity during simulated transient contractions (TCs) of the bladder wall. Simulated TCs caused bursts of afferent activity that were nearly abolished by retigabine. The effects of retigabine were blocked by co‐incubation with XE‐991, suggesting specific activation of KV7 channels on afferent nerves. These results indicate that retigabine primarily affects urinary bladder function by inhibiting TC generation and afferent nerve activity, which are key to sensing bladder fullness. Any direct inhibition of UBSM contractility is likely to be from non‐specific effects on VDCCs and KV2 channels.

show abstract

Section: Introductionmentioning

confidence: 99%

The K_V7 channel activator retigabine suppresses mouse urinary bladder afferent nerve activity without affecting detrusor smooth muscle K⁺ channel currents

Tykocki

Heppner

Dalsgaard³

et al. 2018

The Journal of Physiology

View full text Add to dashboard Cite

show abstract

St. Louis Encephalitis

Cited by 1 publication

References 0 publications

The K_V7 channel activator retigabine suppresses mouse urinary bladder afferent nerve activity without affecting detrusor smooth muscle K⁺ channel currents

The K_V7 channel activator retigabine suppresses mouse urinary bladder afferent nerve activity without affecting detrusor smooth muscle K⁺ channel currents

Contact Info

Product

Resources

About

St. Louis Encephalitis

Cited by 1 publication

References 0 publications

The KV7 channel activator retigabine suppresses mouse urinary bladder afferent nerve activity without affecting detrusor smooth muscle K+ channel currents

The KV7 channel activator retigabine suppresses mouse urinary bladder afferent nerve activity without affecting detrusor smooth muscle K+ channel currents

Contact Info

Product

Resources

About

The K_V7 channel activator retigabine suppresses mouse urinary bladder afferent nerve activity without affecting detrusor smooth muscle K⁺ channel currents

The K_V7 channel activator retigabine suppresses mouse urinary bladder afferent nerve activity without affecting detrusor smooth muscle K⁺ channel currents