1.Effects of Vigabatrin on Pilocarpine-Induced Seizures in Immature Rats.
Bo Ram CHOE ; In Goo LEE ; Kyung Tae WHANG
Journal of the Korean Pediatric Society 2001;44(2):185-192
PURPOSE: Vigabatrin is a widely used antiepileptic drug that greatly increases whole brain gamma- aminobutyric acid(GABA). But little is known about the anticonvulsant effect of vigabatrin on pilocarpine-induced seizures in the immature rats. This study was conducted to determine the effects of vigabatrin on pilocarpine-induced seizures in the immature rats. METHODS: Six to eight day old Sprague-Dawley rats were classified into control(n=5) and vigabatrin-treated(n=5) groups that were pretreated with 30mg/kg of vigabatrin. Animals received vigabatrin or saline, intraperitonealy, for 6 days, once a day. And on the 5th day, right and left cortical electrodes were placed in 10-14 day old animals using stereotaxic instrument. The following day 2.5-hour EEG recordings were obtained to monitor the latency to first electrographic seizures and to first status epilepticus induced by intraperitoneal injection of pilocarpine(200mg/kg). Data were analyzed using the log-rank test. RESULTS: Electrographic seizures and status epilepticus were seen in 80% of vigabatrin-treated group, and in 100% of control group rats. And the latency to first seizure was 8.8+/-2.0 minutes in control group and 20.5+/-5.2 minutes in vigabatrin-treated animals(P<0.02), and to status epilepticus was 12.2+/-1.2 minutes in control group and 29.3+/-6.3 minutes in vigabatrin-treated group(P<0.03). CONCLUSION: It was confirmed that 30mg/kg of vigabatrin administration for 6 days did not affect the body weight gain and behavior of immature rats and had an anticonvulsant effect. These findings might demonstrate that the prolonged latency to seizure, and to status epilepticus, was a time to reduce GABA that was elevated in the brain by vigabatrin administration below the seizure threshold, by pilocarpine.
Animals
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Body Weight
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Brain
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Electrodes
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Electroencephalography
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gamma-Aminobutyric Acid
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Injections, Intraperitoneal
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Pilocarpine
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Rats*
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Rats, Sprague-Dawley
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Seizures*
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Status Epilepticus
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Vigabatrin*
2.Anesthetic management of a preterm neonate intracranial aneurysm clipping.
Bo Ram KIM ; Jun Hyun KIM ; Kyung Woo KIM ; Won Joo CHOE ; Jang Su PARK
Korean Journal of Anesthesiology 2014;67(Suppl):S85-S86
No abstract available.
Humans
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Infant, Newborn*
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Intracranial Aneurysm*
3.Development of a Coronary Aneurysm at a Sirolimus-Eluting Stent-Implanted Lesion in a Patient With Churg-Strauss Syndrome.
Yujung CHO ; Hyunmin CHOE ; Bo Ram KANG ; Min Yong PARK ; Joon Hyung DOH ; Jae Jin KWAK ; Bo Young YOON ; June NAMGUNG ; Sung Yun LEE ; Gam HUR
Korean Circulation Journal 2011;41(9):559-562
A coronary aneurysm (CA) can occur in sirolimus-eluting stent (SES)-implanted coronary lesions. Although several possible mechanisms have been suggested, the precise pathogenesis of a CA in SES-implanted lesions is still unknown. We report a patient with Churg-Strauss syndrome who underwent successful percutaneous coronary intervention with SES and then experienced a CA in an SES-implanted coronary lesion. We describe the CA characteristics through the use of coronary angiography, coronary 64-multidetector computed tomography, and intravascular ultrasound and discuss the etiological factors for the CA in this patient.
Churg-Strauss Syndrome
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Coronary Aneurysm
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Coronary Angiography
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Humans
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Percutaneous Coronary Intervention
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Stents