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中华损伤与修复杂志(电子版) ›› 2022, Vol. 17 ›› Issue (01) : 18 -24. doi: 10.3877/cma.j.issn.1673-9450.2022.01.004

论著

LED红光对糖尿病大鼠创面愈合的影响
李明1, 刘甜甜1, 朱含汀1, 方勇1, 倪涛1,()   
  1. 1. 200011 上海交通大学医学院附属第九人民医院整复外科;200011 上海交通大学医学院创伤研究所
  • 收稿日期:2021-11-03 出版日期:2022-02-01
  • 通信作者: 倪涛
  • 基金资助:
    上海市临床重点专科建设项目-整形外科(shslczdzk00901); 上海交通大学医学院附属第九人民医院交叉基金(JYJC202101)

Effects of LED red light on wound healing in diabetic rats

Ming Li1, Tiantian Liu1, Hanting Zhu1, Yong Fang1, Tao Ni1,()   

  1. 1. Department of Plastic and Reconstructive Surgery, Shanghai Ninth People′s Hospital, Shanghai Jiaotong University School of Medicine, Shanghai 200011, China; Institute of Trauma, Shanghai Jiaotong University School of Medicine, Shanghai 200011, China
  • Received:2021-11-03 Published:2022-02-01
  • Corresponding author: Tao Ni
引用本文:

李明, 刘甜甜, 朱含汀, 方勇, 倪涛. LED红光对糖尿病大鼠创面愈合的影响[J]. 中华损伤与修复杂志(电子版), 2022, 17(01): 18-24.

Ming Li, Tiantian Liu, Hanting Zhu, Yong Fang, Tao Ni. Effects of LED red light on wound healing in diabetic rats[J]. Chinese Journal of Injury Repair and Wound Healing(Electronic Edition), 2022, 17(01): 18-24.

目的

探讨LED红光照射对糖尿病大鼠创面愈合的作用及相关机制。

方法

将30只4周龄雄性SD大鼠按随机数字表法分为正常创面组、糖尿病创面组、红光治疗糖尿病创面组,每组10只。红光治疗糖尿病创面组及糖尿病创面组大鼠高脂饮食4周,正常创面组大鼠正常饮食。饲养4周后对红光治疗糖尿病创面组及糖尿病创面组大鼠按50 mg/kg的量腹腔注射10 mg/mL的链脲佐菌素(STZ)制作糖尿病大鼠模型,2组大鼠均造模成功。造模成功后在3组大鼠的背部两侧各制造2个1.5 cm×1.5 cm的全层皮肤缺损创面,每2 d对大鼠创面进行酒精消毒1次,红光治疗糖尿病创面组大鼠每次消毒后对创面进行LED红光照射5 min,能量密度为20 J/cm2,另外2组大鼠不进行LED红光照射。在观察第7、10、14、21天,观察红光治疗糖尿病创面组大鼠创面有无出现皮疹、红肿、水疱、烫伤等光照不良反应;肉眼观察3组大鼠创面愈合情况;统计3组大鼠创面愈合率。观察第10天从各组随机取2只大鼠,处死后取背部创面组织,固定后,进行苏木精-伊红染色观察创面新生血管情况及肉芽组织生长情况;采用免疫荧光法检测各组大鼠创面组织中CD34、血管内皮细胞生长因子(VEGF)表达情况。数据比较采用单因素方差分析和LSD-t检验。

结果

观察第7、10、14、21天,红光治疗糖尿病创面组大鼠经LED红光照射后皮肤未见皮疹、红肿、水疱、烫伤等光照不良反应。在各个观察时间点,肉眼观察正常创面组及红光治疗糖尿病创面组创面愈合情况均优于糖尿病创面组,且正常创面组创面愈合情况略优于红光治疗糖尿病创面组;观察第7、10、14、21天,正常创面组的创面愈合率分别为(34.62±2.116)%、(53.83±7.92)%、(70.20±5.41)%、(95.65±2.58)%,红光治疗糖尿病创面组创面愈合率分别为(31.76±2.44)%、(50.48±4.54)%、(66.26±11.35)%、(93.96±2.80)%,糖尿病创面组创面愈合率分别为(23.67±4.18)%、(42.71±3.40)%、(53.77±7.74)%、(84.07±4.43)%,3组比较差异均有统计学意义(F=34.69、10.35、10.32、34.40,P<0.05);观察第7、10、14、21天,正常创面组及红光治疗糖尿病创面组创面愈合率始终高于糖尿病创面组,差异均有统计学意义(P<0.05);观察第7、10天,正常创面组创面愈合率高于红光治疗糖尿病创面组,差异均有统计学意义(t=2.80、3.26,P<0.05),观察第14、21天,正常创面组创面愈合率仍高于红光治疗糖尿病创面组,但差异均无统计学意义(t=1.16、1.40,P>0.05)。观察第10天,创面组织苏木精-伊红染色显示,正常创面组内含大量新生毛细血管,肉芽组织内胶原及细胞排列紧密有序;红光治疗糖尿病创面组见较多新生毛细血管,肉芽组织内胶原及细胞较多,但少于正常创面组;而糖尿病创面组新生血管最少,肉芽组织内细胞及胶原稀疏。免疫荧光法检测创面组织中CD34、VEGF表达情况可见,正常创面组CD34、VEGF表达高于红光治疗糖尿病创面组,而红光治疗糖尿病创面组表达高于糖尿病创面组。

结论

LED红光可促进糖尿病大鼠创面组织中CD34、VEGF表达,促进血管新生,进而促进创面愈合。

Objective

To investigate the effect and related mechanism of LED red light irradiation on wound healing in diabetic rats.

Methods

Thirty 4-week-old male SD rats were divided into 3 groups, normal wound group, diabetic wound group, and diabetic wound treated with red light group according to the random number table method, with 10 rats in each group. The rats in diabetic wound treated with red light group and diabetic wound group had a high-fat diet for 4 weeks, and the rats in the normal wound group had a normal diet. After 4 weeks, the rats in the diabetic wound treated with red light group and the diabetic wound group were intraperitoneally injected with 10 mg/mL Streptozotocin (STZ) at a dose of 50 mg/kg to make diabetes models and both groups of rats were successfully modeled. After successful modeling, two full-thickness skin defect wounds of 1.5 cm×1.5 cm were made on both sides of the backs of the three groups of rats, and the wounds of the rats were disinfected with alcohol every two days, and the wounds of the rats in the diabetic wound treated with red light group were irradiated with LED red light at energy density of 20 J/cm2 for 5 minutes after the disfection, the other two groups of rats were not irradiated with LED red light. On the 7th, 10th, 14th, and 21st days of observation, whether there were rashes, redness, blisters, scalds and other adverse light reactions on the wounds of the rats in the diabetic wound treated with red light group were observed, the wound healing condition of the three groups of rats was observed by naked eye, and the wound healing rate of the three groups of rats was counted. On the 10th day of observation, 2 rats were randomly selected from each group, and the back wound tissue was taken after being sacrificed. After fixation, hematoxylin-eosin staining was performed to observe the condition of new blood vessels and the growth of granulation tissue on the wound surface; the expressions of CD34 and vascular endothelial growth factor (VEGF) in wound tissue of rats in each group were detected by immunofluorescence method. Data were compared with one-way ANOVA and LSD-t test.

Results

On the 7th, 10th, 14th, and 21st days, the rats in the diabetic wound treated with red light group were irradiated with LED red light, and there were no adverse light reactions such as rash, redness, blisters, and burns on the skin. At each observation time point, the wound healing of the normal wound group and the diabetic wound treated with red light group was better than that of the diabetic wound group by naked eye observation, and the wound healing of the normal wound group was slightly better than that of the diabetic wound treated with red light group. On the 7th, 10th, 14th, and 21st days of observation, the wound healing rates of the normal wound group were (34.62±2.116)%, (53.83±7.92)%, (70.20±5.41)%, and (95.65±2.58)%, the wound healing rates of the diabetic wound treated with red light group were (31.76±2.44)%, (50.48±4.54)%, (66.26±11.35)% and (93.96±2.80)%, and the wound healing rates of the diabetic wound group were (23.67±4.18)%, (42.71±3.40)%, (53.77±7.74)%, (84.07±4.43)%, respectively, the differences between the three groups were statistically significant (F=34.69, 10.35, 10.32, 34.40; P<0.05). On the 7th, 10th, 14th, and 21st days of observation, the wound healing rates of the normal wound group and the diabetic wound treated with red light group were always higher than those of the diabetic wound group, and the differences were statistically significant (P<0.05). On the 7th and 10th days of observation, the wound healing rates of the normal wound group were higher than those of the diabetic wound treated with red light group, and the differences were statistically significant (t=2.80, 3.26; P<0.05). On the 14th and 21st days of observation, the wound healing rates of the normal wound group were still higher than those of the diabetic wound treated with red light group, but the differences were no statistically significant (t=1.16, 1.40; P>0.05). On the 10th day of observation, hematoxylin-eosin staining of the wound tissue showed that the normal wound group contained a large number of new capillaries, and the collagen and cells in the granulation tissue were arranged in a tight and orderly manner; the diabetic wound treated with red light group saw some new capillaries, there were lots of collagen and cells in the granulation tissue, but less than that in the normal wound group; while the diabetic wound group had the least amount of new blood vessels, and the cells and collagen in the granulation tissue were sparse. The expressions of CD34 and VEGF were observed by immunofluorescence, the expressions of CD34 and VEGF in the normal wound group were higher than those of the diabetic wound treated with red light group, while the expressions of CD34 and VEGF in the diabetic wound treated with red light group were higher than those of the diabetic wound group.

Conclusion

LED red light can promote the expression of CD34 and VEGF in the wound tissue of diabetic rats, promote angiogenesis, and then promote wound healing.

表1 3组大鼠不同观察时间点创面愈合率的比较(%, ±s)
图1 3组大鼠不同观察时间点创面愈合情况
图2 观察第10天,3组大鼠创面血管化及肉芽组织形成情况(苏木精-伊红染色,×200,黑色箭头标记为毛细血管,图中标尺为100 μm)。A示正常创面组可见大量新生毛细血管,肉芽组织内细胞及胶原紧密,呈平行排列;B示红光治疗糖尿病创面组见较多新生毛细血管及新生胶原纤维,细胞排列较为致密;C示糖尿病创面组,新生毛细血管较少,成纤维细胞较少,细胞排列稀疏
图3 观察第10天,3组大鼠创面组织中CD34表达情况(免疫荧光染色,×200,细胞核显色:蓝色,CD34显色:红色,红色箭头标记部分新生毛细血管,图中标尺为100 μm)。A示正常创面组可见大量CD34+细胞,其形成的管状结构为新生毛细血管;B示红光治疗糖尿病创面组可见较多CD34+细胞,其新生毛细血管较多;C示糖尿病创面组CD34+细胞较少,新生毛细血管少
图4 观察第10天,3组大鼠创面组织中VEGF表达情况(免疫荧光染色,200,细胞核显色:蓝色,VEGF显色:红色,红色箭头标记部分VEGF,图中标尺为100 μm)。A示正常创面组可见大量VEGF表达,数量和强度最高;B示红光治疗糖尿病创面组可见VEGF表达,数量较多;C示糖尿病创面组细胞数量少,VEGF表达少,强度低;VEGF为血管内皮细胞生长因子
[1]
Zheng Y, Ley SH, Hu FB. Global aetiology and epidemiology of type 2 diabetes mellitus and its complications[J]. Nat Rev Endocrinol, 2018, 14(2): 88-98.
[2]
Saeedi P, Petersohn I, Salpea P, et al. Global and regional diabetes prevalence estimates for 2019 and projections for 2030 and 2045: Results from the International Diabetes Federation Diabetes Atlas, 9th edition[J]. Diabetes Res Clin Pract, 2019, 157: 107843.
[3]
Dinh TL, Veves A. A review of the mechanisms implicated in the pathogenesis of the diabetic foot[J]. Int J Low Extrem Wounds, 2005, 4(3): 154-159.
[4]
Veves A, Akbari CM, Primavera J, et al. Endothelial dysfunction and the expression of endothelial nitric oxide synthetase in diabetic neuropathy, vascular disease, and foot ulceration[J]. Diabetes, 1998, 47(3): 457-463.
[5]
Singh N, Armstrong DG, Lipsky BA. Preventing foot ulcers in patients with diabetes[J]. JAMA, 2005, 293(2): 217-228.
[6]
Bowling FL, Rashid ST, Boulton AJ. Preventing and treating foot complications associated with diabetes mellitus[J]. Nat Rev Endocrinol, 2015, 11(10): 606-616.
[7]
Armstrong DG, Boulton AJM, Bus SA. Diabetic Foot Ulcers and Their Recurrence[J]. N Engl J Med, 2017, 376(24): 2367-2375.
[8]
Anders JJ, Lanzafame RJ, Arany PR. Low-level light/laser therapy versus photobiomodulation therapy[J]. Photomed Laser Surg, 2015, 33(4): 183-184.
[9]
Tsai SR, Hamblin MR. Biological effects and medical applications of infrared radiation[J]. J Photochem Photobiol B, 2017, 170: 197-207.
[10]
Rohringer S, Holnthoner W, Chaudary S, et al. The impact of wavelengths of LED light-therapy on endothelial cells[J]. Sci Rep, 2017, 7(1): 10700.
[11]
Yadav A, Gupta A. Noninvasive red and near-infrared wavelength-induced photobiomodulation: promoting impaired cutaneous wound healing[J]. Photodermatol Photoimmunol Photomed, 2017, 33(1): 4-13.
[12]
占利民,方林森,王晨,等. 糖尿病足的治疗进展[J]. 实用糖尿病杂志2020, 16(6): 84-86.
[13]
Finsen N. Om Anvevendelsei Medicinenaf Koncentrerede Kemiske Lysstraaler[M]. Copenhagen: Gyldendalske Boghandels Forlag, 1886: 5-52.
[14]
Grzybowski A, Pietrzak K. From patient to discoverer-Niels Ryberg Finsen (1860-1904)-the founder of phototherapy in dermatology[J]. Clin Dermatol, 2012, 30(4): 451-455.
[15]
Maiman TH. Stimulated Optical Radiation in Ruby[J]. Nature, 1960, 187(4736): 493-494.
[16]
Mester E, Szende B, Gärtner P. The effect of laser beams on the growth of hair in mice[J]. Radiobiol Radiother (Berl), 1968, 9(5): 621-626.
[17]
Sugawara H, Ishikawa M, Hatakoshi G. High-efficiency InGaAlP/GaAs visible light-emitting diodes[J]. Appl Phys Lett, 1991, 58(10): 1010-1012.
[18]
Heiskanen V, Hamblin MR. Photobiomodulation: lasers vs. light emitting diodes?[J]. Photochem Photobiol Sci, 2018, 17(8): 1003-1017.
[19]
Frangež I, Nizi-Kos T, Frangež HB. Phototherapy with LED Shows Promising Results in Healing Chronic Wounds in Diabetes Mellitus Patients: A Prospective Randomized Double-Blind Study[J]. Photomed Laser Surg, 2018, 36(7): 377-382.
[20]
de Alencar Fonseca Santos J, Campelo MBD, de Oliveira RA, et al. Effects of Low-Power Light Therapy on the Tissue Repair Process of Chronic Wounds in Diabetic Feet[J]. Photomed Laser Surg, 2018, 36(6): 298-304.
[21]
熊臻,邹晓芳,杨静,等. 红光治疗在难愈性创面的临床应用及研究进展[J]. 皮肤病与性病2020, 42(2): 178-180.
[22]
Amirsadeghi A, Jafari A, Eggermont LJ, et al. Vascularization strategies for skin tissue engineering[J]. Biomater Sci, 2020, 8(15): 4073-4094.
[23]
Kaushik K, Das A. Endothelial progenitor cell therapy for chronic wound tissue regeneration[J]. Cytotherapy, 2019, 21(11): 1137-1150.
[24]
Fina L, Molgaard HV, Robertson D, et al. Expression of the CD34 gene in vascular endothelial cells[J]. Blood, 1990, 75(12): 2417-2426.
[25]
Gangenahalli GU, Singh VK, Verma YK, et al. Hematopoietic stem cell antigen CD34: role in adhesion or homing[J]. Stem Cells Dev, 2006, 15(3): 305-313.
[26]
Melincovici CS, Boşca AB, Şuşman S, et al. Vascular endothelial growth factor (VEGF)- key factor in normal and pathological angiogenesis[J]. Rom J Morphol Embryol, 2018, 59(2): 455-467.
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