ATP-sensitive potassium channels mediate the anti-ischemic properties of ischemic and pharmacologic preconditioning in rat random-pattern skin flap

Azadeh Beheshtian, Shadpour Demehri, Saman Kiumehr, Amirali Hassanzadeh Salmasi, Behtash Ghazinezami, Sina Rahimpour, Saeed Amanpour, Shahram Rabbani, Mohammad Ali Mohagheghi, Ahmad Reza Dehpour

Research output: Contribution to journalArticle

Abstract

Ischemic preconditioning (IPC) and pharmacologic preconditioning by morphine and adenosine may significantly decrease the amount of necrosis in rat random pattern skin flaps. We examined the role of ATP-sensitive potassium channels (KATP channels) in mediating these protective phenomenon by using glibenclamide a nonspecific blocker of these channels. We also investigated whether administration of diazoxide an opener of the KATP channels could mimic the same protective effect.Ninety male Sprague-Dawley rats were randomly divided into either control or treatment groups (n = 6 each). Bipedicled dorsal skin flaps (2 × 8 cm) were elevated at the midline. In pharmacologic preconditioning groups, 1 mL of morphine (5 mg/flap), adenosine (0.5 mg/flap), or different doses of diazoxide (0.5, 1, 5, and 15 mg/flap) were administered locally in the cranial half of the flap, respectively. One milliliter of saline was locally injected in the control group. In the IPC group, 1 hour after local saline injection the cranial pedicle was clamped for 20 minutes, and then 40 minutes' reperfusion was performed. In another experiment, 0.3 mg/kg of glibenclamide was injected intraperitoneally 30 minutes before local administration of saline or drug in ischemic or pharmacologic preconditioning groups. Regardless of the group, all flaps were cut at the cranial side 2 hours after elevation and were sutured back. Flap survival area was evaluated on the seventh postoperative day. IPC and pharmacologic preconditioning with morphine, adenosine, and diazoxide (in higher doses; 1, 5, and 15 mg/flap) improved survival area compared with the control group. Glibenclamide abolished their protective effect.KATP channels may have a key role in anti-ischemic properties of IPC and pharmacologic preconditioning.

Original languageEnglish (US)
Pages (from-to)94-99
Number of pages6
JournalAnnals of Plastic Surgery
Volume57
Issue number1
DOIs
StatePublished - Jul 2006
Externally publishedYes

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KATP Channels
Ischemic Preconditioning
Diazoxide
Glyburide
Adenosine
Morphine
Skin
Control Groups
Reperfusion
Sprague Dawley Rats
Necrosis
Injections
Pharmaceutical Preparations
Therapeutics

Keywords

  • Adenosine
  • Diazoxide
  • Flap
  • Ischemic
  • KATP channel
  • Morphine
  • Pharmacologic
  • Preconditioning
  • Random pattern
  • Skin

ASJC Scopus subject areas

  • Surgery

Cite this

ATP-sensitive potassium channels mediate the anti-ischemic properties of ischemic and pharmacologic preconditioning in rat random-pattern skin flap. / Beheshtian, Azadeh; Demehri, Shadpour; Kiumehr, Saman; Salmasi, Amirali Hassanzadeh; Ghazinezami, Behtash; Rahimpour, Sina; Amanpour, Saeed; Rabbani, Shahram; Mohagheghi, Mohammad Ali; Dehpour, Ahmad Reza.

In: Annals of Plastic Surgery, Vol. 57, No. 1, 07.2006, p. 94-99.

Research output: Contribution to journalArticle

Beheshtian, A, Demehri, S, Kiumehr, S, Salmasi, AH, Ghazinezami, B, Rahimpour, S, Amanpour, S, Rabbani, S, Mohagheghi, MA & Dehpour, AR 2006, 'ATP-sensitive potassium channels mediate the anti-ischemic properties of ischemic and pharmacologic preconditioning in rat random-pattern skin flap', Annals of Plastic Surgery, vol. 57, no. 1, pp. 94-99. https://doi.org/10.1097/01.sap.0000214872.13634.d4
Beheshtian, Azadeh ; Demehri, Shadpour ; Kiumehr, Saman ; Salmasi, Amirali Hassanzadeh ; Ghazinezami, Behtash ; Rahimpour, Sina ; Amanpour, Saeed ; Rabbani, Shahram ; Mohagheghi, Mohammad Ali ; Dehpour, Ahmad Reza. / ATP-sensitive potassium channels mediate the anti-ischemic properties of ischemic and pharmacologic preconditioning in rat random-pattern skin flap. In: Annals of Plastic Surgery. 2006 ; Vol. 57, No. 1. pp. 94-99.
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AU - Demehri, Shadpour

AU - Kiumehr, Saman

AU - Salmasi, Amirali Hassanzadeh

AU - Ghazinezami, Behtash

AU - Rahimpour, Sina

AU - Amanpour, Saeed

AU - Rabbani, Shahram

AU - Mohagheghi, Mohammad Ali

AU - Dehpour, Ahmad Reza

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N2 - Ischemic preconditioning (IPC) and pharmacologic preconditioning by morphine and adenosine may significantly decrease the amount of necrosis in rat random pattern skin flaps. We examined the role of ATP-sensitive potassium channels (KATP channels) in mediating these protective phenomenon by using glibenclamide a nonspecific blocker of these channels. We also investigated whether administration of diazoxide an opener of the KATP channels could mimic the same protective effect.Ninety male Sprague-Dawley rats were randomly divided into either control or treatment groups (n = 6 each). Bipedicled dorsal skin flaps (2 × 8 cm) were elevated at the midline. In pharmacologic preconditioning groups, 1 mL of morphine (5 mg/flap), adenosine (0.5 mg/flap), or different doses of diazoxide (0.5, 1, 5, and 15 mg/flap) were administered locally in the cranial half of the flap, respectively. One milliliter of saline was locally injected in the control group. In the IPC group, 1 hour after local saline injection the cranial pedicle was clamped for 20 minutes, and then 40 minutes' reperfusion was performed. In another experiment, 0.3 mg/kg of glibenclamide was injected intraperitoneally 30 minutes before local administration of saline or drug in ischemic or pharmacologic preconditioning groups. Regardless of the group, all flaps were cut at the cranial side 2 hours after elevation and were sutured back. Flap survival area was evaluated on the seventh postoperative day. IPC and pharmacologic preconditioning with morphine, adenosine, and diazoxide (in higher doses; 1, 5, and 15 mg/flap) improved survival area compared with the control group. Glibenclamide abolished their protective effect.KATP channels may have a key role in anti-ischemic properties of IPC and pharmacologic preconditioning.

AB - Ischemic preconditioning (IPC) and pharmacologic preconditioning by morphine and adenosine may significantly decrease the amount of necrosis in rat random pattern skin flaps. We examined the role of ATP-sensitive potassium channels (KATP channels) in mediating these protective phenomenon by using glibenclamide a nonspecific blocker of these channels. We also investigated whether administration of diazoxide an opener of the KATP channels could mimic the same protective effect.Ninety male Sprague-Dawley rats were randomly divided into either control or treatment groups (n = 6 each). Bipedicled dorsal skin flaps (2 × 8 cm) were elevated at the midline. In pharmacologic preconditioning groups, 1 mL of morphine (5 mg/flap), adenosine (0.5 mg/flap), or different doses of diazoxide (0.5, 1, 5, and 15 mg/flap) were administered locally in the cranial half of the flap, respectively. One milliliter of saline was locally injected in the control group. In the IPC group, 1 hour after local saline injection the cranial pedicle was clamped for 20 minutes, and then 40 minutes' reperfusion was performed. In another experiment, 0.3 mg/kg of glibenclamide was injected intraperitoneally 30 minutes before local administration of saline or drug in ischemic or pharmacologic preconditioning groups. Regardless of the group, all flaps were cut at the cranial side 2 hours after elevation and were sutured back. Flap survival area was evaluated on the seventh postoperative day. IPC and pharmacologic preconditioning with morphine, adenosine, and diazoxide (in higher doses; 1, 5, and 15 mg/flap) improved survival area compared with the control group. Glibenclamide abolished their protective effect.KATP channels may have a key role in anti-ischemic properties of IPC and pharmacologic preconditioning.

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