Kim Hye One, Jin Cheol Kim, Yu Gyeong Kong, In Suk Kwak
Department of Dermatology, Kangnam Sacred Heart Hospital, Hallym University College of Medicine, Seoul 07441, Korea.
Department of Anesthesiology and Pain Medicine, Burn Center, Hangang Sacred Heart Hospital, Hallym University College of Medicine, 94-200 Yeoungdeungpo-dong, Yeoungdeungpo-gu, Seoul 150-710, Korea.
Medicina (Kaunas). 2020 Oct 25;56(11):560. doi: 10.3390/medicina56110560.
Postburn pruritus is a common complication of scars in burn patients. In our previous study, we discovered increased expression of TRPV3, TRPV4, and TRPA1. Among them, TRPV3, in particular, is predominantly expressed in the epidermis of the tissue of pruritic burn scars. We sought to evaluate the correlation between the expression of TRPV3 activators and itching after application of TRPV3 activator carvacrol over burn scars. Design: This was a double-blind clinical trial with non-randomized distribution.
This study was performed in a hospital setting.
Patients with itching of burn scars (numerical rating scale (NRS), <3; = 8; Group 1 and NRS, ≥3; = 16, Group 2) and healthy volunteers ( = 18, Group 3) were included.
The investigational drug carvacrol (100%, 75%, and 50%) and control drug (10% ethanol) were applied over the scars using IQ Ultimate™ 1 × 1 cm chamber sheets.
The presence of pruritus, erythema, edema, and other skin lesions was evaluated. The verbal NRS scores were also compared. Carvacrol induced more itching in Group 2 than in Groups 1 and 3. In Group 2, 100%, 75%, and 50% carvacrol caused significantly more itching (NRS score, 5.18 ± 3.04, 5.18 ± 3.04, and 4.93 ± 2.96, respectively) than that in Group 1 (NRS score, 1.00 ± 1.80, 1.00 ± 1.80, and 1.00 ± 1.80, respectively) and Group 3 (NRS score, 2.38 ± 1.94, 1.27 ± 1.32, respectively). The TRPV3 activator carvacrol can cause itching if applied over burn scars. This study can help understand the mechanism and prognosis of post-burn itching and contribute to the development of its treatment.
烧伤后瘙痒是烧伤患者瘢痕常见的并发症。在我们之前的研究中,我们发现瞬时受体电位香草酸亚型3(TRPV3)、瞬时受体电位香草酸亚型4(TRPV4)和瞬时受体电位锚蛋白1(TRPA1)的表达增加。其中,TRPV3尤其主要在瘙痒性烧伤瘢痕组织的表皮中表达。我们试图评估在烧伤瘢痕上应用TRPV3激活剂香芹酚后,TRPV3激活剂的表达与瘙痒之间的相关性。设计:这是一项非随机分配的双盲临床试验。
本研究在医院环境中进行。
纳入有烧伤瘢痕瘙痒的患者(数字评分量表(NRS),<3;n = 8;第1组)和NRS≥3;n = 16,第2组)以及健康志愿者(n = 18,第3组)。
使用IQ Ultimate™ 1×1 cm腔室片将研究药物香芹酚(100%、75%和50%)和对照药物(10%乙醇)涂抹在瘢痕上。
评估瘙痒、红斑、水肿和其他皮肤病变的存在情况。还比较了语言NRS评分。香芹酚在第2组中引起的瘙痒比第1组和第3组更多。在第2组中,100%、75%和50%的香芹酚引起的瘙痒(NRS评分分别为5.18±3.04、5.18±3.04和4.93±2.96)明显多于第1组(NRS评分分别为1.00±1.80、1.00±1.80和1.00±1.80)和第3组(NRS评分分别为2.38±1.94、1.27±1.32)。TRPV3激活剂香芹酚如果涂抹在烧伤瘢痕上会引起瘙痒。本研究有助于了解烧伤后瘙痒的机制和预后,并有助于其治疗的发展。