Ultrasound imaging of chitosan nerve conduits that bridge sciatic nerve defects in rats

Ultrasound imaging of chitosan nerve conduits that bridge sciatic nerve defects in rats

The repair of peripheral nerve injuries with autologous nerve remains the gold standard (Wang et al., 2005; Yao et al., 2010; Deal et al., 2012; Kriebel et al., 2014; Liu et al., 2014; Tamaki et al., 2014; Yu et al., 2014; Zhu and Lou, 2014). With advances in tissue engineering and biomaterials, tissue-engineered nerve conduits with various biomaterials and structures, such as collagen and chitosan nerve conduits, have already been used in the clinic as alternatives to autologous nerve in the repair of peripheral nerve injury (Wang et al., 2012; Svíženská et al., 2013; Eppenberger et al., 2014; Gu et al., 2014; Koudehi et al., 2014; Moya-Díaz et al., 2014; Novajra et al., 2014; Okamoto et al., 2014; Shea et al., 2014; Singh et al., 2014; Tamaki et al., 2014; Yu et al., 2014). Therefore, new simple and effective methods are needed to better evaluate the outcomes of repair using nerve conduits in vivo. Ultrasound is a common noninvasive clinical detection modality that has been used in many fi elds. However, ultrasound has only rarely been used to observe implanted nerve conduits in vivo. Haug et al. (2013) tried to displace the collagen nerve conduit for repairing the digital nerve under ultrasound. Here, we report the fi rst use of ultrasound to noninvasively observe the changes in chitosan nerve conduits implanted in rats over time.

Chitosan (Nantong Xincheng Biochemical Company, Nantong, Jiangsu Province, China) was puri fi ed twice by dissolution in 10 g of acetic acid, fi ltration, precipitation with 50 g of NaOH, and fi nally drying in a vacuum at room temperature. The degree of chitosan deacetylation was 92.3% as measured by titration. After 5 g of chitosan had completely dissolved in 100 mL of 0.15 mol/L hydrochloric acid, 10% gelatin and then 5 g of chitin powder were added while stirring, forming an opaque viscous liquid. The chitin/chitosan mixture was then injected into stainless-steel casting molds, which were then sealed and placed at -12°C for 2-4 hours. The frozen gels were removed and soaked in 4 mol/L NaOH for 4 hours to neutralize any remaining lactic acid and to complete solidi fi cation. The conduits were rinsed repeatedly with distilled water to remove any residual NaOH and sodium lactate and lyophilized under a 35-45 mTorr vacuum for 20 hours. The resulting porous conduits were 2 mm inner diameter, 3 mm outer diameter, and 80 mm long (Yang et al., 2011).

A total of 21 clean, female, 2-month-old Sprague-Dawley rats were provided by the Experimental Animal Center of Nantong University, China (license No. SCXK (Su) 2008-0010). The animals were housed in a temperature-controlled environment and allowed food and water ad libitum. All experimental protocols were approved by the Administration Committee of Experimental Animals, Jiangsu Province, China, in accordance with the guidelines of the Institutional Animal Care and Use Committee, Nantong University, China. The rats were deeply anesthetized with an intraperitoneal injection of a compound anesthetic (chloral hydrate: 4.25 g, magnesium sulfate: 2.12 g, sodium pentobarbital: 886 mg, ethanol: 14.25 mL, and propylene glycol: 33.8 mL in 100 mL) at a dose of 0.2-0.3 mL/100 g. The skin and muscle were incised to expose the sciatic nerve at the left mid-thigh. An 8-mm segment of the sciatic nerve (from about 10 mm distal to the proximal end to the ischial tuberosity) was resected to produce a 10-mm gap after slight retraction of the distal and proximal stumps. The nerve gap was bridged by a chitosan nerve conduit, and the proximal and distal nerve stumps were inserted into the two ends of the conduit (1 mm was inserted for each end). Then, the muscle layers were closed with sutures, and the skin was closed with wound clips. After surgery, the animals were placed in warmed cages (Yang et al., 2011).

At 1, 2, 3, 4, 8, 12, and 24 weeks after surgery (n = 3 in each group), the rats were again deeply anesthetized with the compound anesthetic. A B-mode ultrasound (HIVISION Avius, HITACHI, Chiba Kashiwa, Japan) equipped with a high-resolution linear transducer with a frequency range of 7.5 to 10 MHz and a gel pad serving as an interface between the transducer and fur was used to detect the nerve conduit implanted in the rat. After ultrasound imaging, the surgical site at the left midthigh was reopened to expose the nerve conduit. The length and outer diameter were measured with a ruler after photographing the nerve conduit. The ultrasound imaging clearly showed the longitudinal section, as well as the distal and proximal nerves and cross section of the nerve conduit surrounded by muscles (Figure 1). The length and outer diameter of the nerve conduit measured by ultrasound were not different (P ＞0.05) than those measured by ruler after dissection at the different time points (Figure 2).

In addition, decreases in both the length and outer diameter were seen from 12 to 24 weeks. The decrease in length (P ＜ 0.05) from 12 to 24 weeks was more evident, and this difference reflected the degradation mode of the nerve conduit in vivo in rat. There was no evident fracture or collapse of the nerve conduit. However, the two ends of the nerve conduit had clearly shortened at 24 weeks, and a moderate collapse of the cross section was also observed at 24 weeks (Figures 1 and 2).

The strain ratio of the nerve conduit was also measured with ultrasound, which reflects the elasticity of the nerve conduit wall. The gradual increase in the strain ratio of the nerve conduit over time suggests that the nerve conduit degraded in vivo (Figure 3).

Based on these results, the morphological changes of the nerve conduit can be observed by ultrasound imaging in vivo. In addition, the strain ratio measured by ultrasound may be an objective re fl ection of the degradation of the nerve conduit in vivo. Moreover, any unsatisfactory complications after implantation, such as fracture, collapse, bleeding, or unusual swelling of the nerve conduits, may be easily identi fi ed.

However, some factors are related to the effect of ultrasound detection closely. A specialized training is necessary to identify the peripheral nerve and nerve conduit for the ultrasound detector. The image resolution is relative to the ultrasound frequency. Different frequencies maybe suitable for different conduits made of different biomaterials. Because the rat was small on volume, which has a limited absorption capacity of biomaterials, the degradation of chitosan in vivo seemed relatively slow. Also we attempted to detect the dog, a bigger animal, with ultrasound and the trend of degradation of conduit was earlier and more evident.

Ultrasound, as a noninvasive imaging modality, can be used as a supplementary observation method during conventional animal experiments on peripheral nerve tissue engineering.

Figure 1 Ultrasound imaging of the morphology of a chitosan nerve conduit in a rat model of sciatic nerve defects after implantation.

Figure 2 Length (A) and outer diameter (B) of the nerve conduit measured by ultrasound and with a ruler after dissection.

Figure 3 Ultrasound imaging of the elasticity of the chitosan nerve conduit in a rat model of sciatic nerve defects after implantation.

Xiaoyang Chen2, Yifei Yin2, Tingting Zhang2, Yahong Zhao3, Yumin Yang3, Xiaomei Yu2, Hongkui Wang1,3

1 School of Biology and Basic Medical Sciences, Soochow University, Suzhou, Jiangsu Province, China

2 Department of Doppler Ultrasound, A ffi liated Hospital of Nantong University, Nantong, Jiangsu Province, China

3 Jiangsu Key Laboratory of Neuroregeneration, Nantong University, Nantong, Jiangsu Province, China

Xiaoyang Chen and Yifei Yin contributed equally to this work.

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Copyedited by McCarty W, Stow A, Yu J, Qiu Y, Li CH, Song LP, Zhao M

Hongkui Wang, School of Biology and Basic Medical Sciences, Soochow University, Suzhou 215123, Jiangsu Province, China; Jiangsu Key Laboratory of Neuroregeneration, Nantong University, Nantong, Jiangsu Province, China, wang-hongkui@ntu.edu.cn.

10.4103/1673-5374.137592 http://www.nrronline.org/

Funding: The research is supported by the National High Technology Research and Development Program of China, No. 2012AA020502; the National Natural Science Foundation of China, No. 81171457 and 81371687; and the Priority of Academic Program Development of Jiangsu Higher Education Institutions.

Author contributions: Yang YM checked and revised this article. Wang HK designed and evaluated this study, and wrote the manuscript. Chen XY and Yin YF designed and performed the experiments. Zhang TT and Zhao YH performed the experiments. Yu XM collected the data. All authors approved the final version of the paper.

Con fl icts of interest: None declared.

Accepted: 2014-06-06

Chen XY, Yin YF, Zhang TT, Zhao YH, Yang YM, Yu XM, Wang HK. Ultrasound imaging of chitosan nerve conduits that bridge sciatic nerve defects in rats. Neural Regen Res. 2014;9(14)：1386-1388.