27 August 2020: Animal Study
Green Tea Polyphenols Promote Functional Recovery from Peripheral Nerve Injury in Rats
Jinhong Chen1ABCDF, Rongyuan Yang1ABCDF, Honghan Li1BCD, Jie Lao2ACDEF*DOI: 10.12659/MSM.923806
Med Sci Monit 2020; 26:e923806
Abstract
BACKGROUND: Peripheral nerve injury (PNI) is a common and progressive disorder with sensory and motor deficits in the peripheral nervous system (PNS). Treatment is difficult, with unfavorable prognosis. Green tea polyphenols (GTPs) exert neuroprotective effects on regeneration of the central nervous system (CNS). However, the effects of GTPs on functional recovery of the PNS have not been fully characterized. Consequently, the present study investigated the effects of GTPs on nerve regeneration of rats with PNI.
MATERIAL AND METHODS: The model of PNI was established in rats by sciatic nerve injury (SNI). Adult male Wistar rats with SNI were randomly divided into a vehicle group and a GTPs group. The compound muscle action potential (CMAP) of rat sciatic nerves (SN) was measured using the CM6240 physiological signal acquisition and processing system. The wet weight of the triceps muscle was determined using an analytical balance. The number of myelinated nerve fibers was counted under an optical microscope. Ultrastructure of the regenerated nerves in SN was observed by transmission electron microscopy. The mRNA and protein expression of nerve growth factor (NGF), growth-associated protein-43 (GAP-43), neurofilament 200 (NF200), and myelin-associated glycoprotein (MAG) in SN stumps were measured by real-time quantification PCR (RT-qPCR) and Western blot, respectively.
RESULTS: In rats with SNI, GTPs relieved the adhesion between nerve anastomosis and surrounding tissues, and significantly increased nerve conduction velocity, wet weight of the triceps muscle, and development and axonal regeneration of myelinated nerve fibers. Moreover, GTPs promoted the mRNA and protein expressions of NGF, GAP-43, NF200, and MAG in SN stumps.
CONCLUSIONS: GTPs promotes nerve regeneration in rats with SNI.
Keywords: Nerve Regeneration, Peripheral Nerve Injuries, polyphenols, Recovery of Function, Sciatic Nerve, Tea
Background
The PNS, which links the CNS (spinal cord and brain) and the rest of body, is fragile and easily damaged. PNI, which results from trauma or acute compression, accounts for approximately 1.5–4.0% of the world’s annual new trauma cases [1]. Nerve regeneration in PNI depends on recovery of limb function, and the nerve growth rate is a key factor in muscular atrophy [2]. Currently, there is no effective therapy for repair of PNI or prevention of muscle atrophy and treatment for nerve regeneration after PNI.
Numerous scholars have explored various treatments for PNI repair, and showed protective effects on nerve regeneration. For instance, laser phototherapy restores denervated muscle atrophy and promotes nerve regeneration of PNI [3], neural conduit is applied for PNI repair [4], 4-aminopyridine (4-AP) promotes recovery of acute PNI and myelin regeneration in rats [2], and vitamin supplements are beneficial for nerve regeneration in acute PNI [5]. However, adverse effects exist, and an accessible, convenient method without adverse effects is urgently needed.
GTPs, the major bioactive compounds of green tea, exert various functions, with anti-oxidation [6], anti-inflammation [7], and anti-cancer [8] effects. In addition, GTPs exhibit protective effects in the CNS. For instance, GTPs stabilize mitochondria in brain neurodegenerative diseases via antioxidants [9], and GTPs alleviate nerve damage after focal cerebral ischemia [10]. However, the effects of GTPs in the PNS have not been investigated. Therefore, the present study was performed to assess the effects of GTPs in the PNS and to lay a theoretical foundation for clinical application of GTPs.
Material and Methods
ANIMALS:
Adult male Wistar rats weighing about 170–190 g were purchased from the Laboratory Animal Center of Fujian Medical University (Fuzhou, China). Rats were kept in stable conditions of 22±3°C, 55% relative humidity, and 12-h light/dark cycle with food/water ad libitum. Animal care and procedures were approved by the Animal Use and Care Committee of Huashan Affiliated Hospital of Fudan University, and the study was performed strictly following the guidelines.
ESTABLISHMENT OF SNI MODEL IN RATS:
After intraperitoneal injection of 10% chloral hydrate (0.5 ml/100 g) into each rat, a longitudinal incision (2.5 cm in length) was made in the posterior part of the right lower limb femur. Under an operating microscope (Carl Zeiss, Germany), the muscular membranes were cut from the gap between the semitendinosus, semimembranosus, and biceps femoris. By the suspension method, the gluteus maximus muscle was stretched, and the SN was fully exposed. The SN was cut with a sterile blade 0.8 cm below the lower edge of the piriformis muscle, and the wound was sutured with aseptic 11-0 noninvasive nylon thread, while the epineurium was sutured with 4–6 needles. Subsequently, the incision was closed layer-by-layer with sterile 1-0 suture. A microsuture was placed on the epineurium of the anastomosis and served as a marker.
GROUPS:
Adult male Wistar rats were randomly divided into 2 groups: a vehicle group and a GTPs group. Rats in the 2 groups underwent end-to-end neurorrhaphy after the right SN was severed. Subsequently, rats in the vehicle group were intraperitoneally injected with saline for 2 weeks, while those in the GTPs group were intraperitoneally injected with GTPs (50 mg/kg/d, Herbking Biotechnology, Xi’an, China) for 2 weeks.
GENERAL OBSERVATION:
At weeks 2, 4, 6, and 8 after establishment of the SNI model in 30 rats, the mental state, activity, healing of the wound, and the occurrence of plantar ulcer in each rat were closely observed, and the color, texture, and adhesion surrounding tissues of the injured SN were also observed. These observations were also made in the 30 rats in the vehicle group.
NEURO-ELECTROPHYSIOLOGICAL EXAMINATION:
At weeks 2, 4, 6, 8, and 12 after SNI, 6 rats were taken from each time-point in the vehicle group and GTPs group and anesthetized by intraperitoneal injection of 20% uratan (0.6 ml/100 g) prior to neuro-electrophysiological examination. Briefly, the muscle was first separated, and the right SN, tibial nerve, common sural nerve, gastrocnemius, and anterior tibial muscle were exposed. Then, the stimulating electrodes were placed 1.0 cm apart in the proximal end and distal end of the nerve junction, while the recording electrode was obliquely inserted at an angle of 45 degrees into the mid-abdomen in the tibialis anterior muscle. The reference electrode was inserted at the tibialis anterior muscle insertion point, while the grounding electrode was inserted into the tissue between the stimulating electrodes and the recording electrode. The CMAP of rat SN was measured using the CM6240 physiological signal acquisition and processing system (Chengdu Instrument Factory, Chengdu, China), with a frequency of 1 Hz, current of 2 mA, and wave length of 0.2 ms, during which the muscles and nerves were kept moist by saline.
MEASUREMENT OF TRICIPITAL MUSCLE WET WEIGHT:
To assess the growth rate after nerve transection and anastomosis, the tricipital muscle wet weight was measured from the 4th week to 12th week after establishment of the SNI model, with 6 rats for each time-point at weeks 4, 6, 8, and 12 after SNI in the vehicle group and GTPs group. After the neuro-electrophysiological examination, the whole tricipital muscle was removed, and the wet weight of the right triceps muscle was weighed using an analytical balance, with the left triceps muscle serving as the control. The muscle recovery rate was calculated by the following formula: ipsilateral tricipital muscle wet weight/contralateral tricipital muscle wet weight ×100%.
OPTICAL MICROSCOPY OBSERVATION:
After the neuro-electrophysiological examination at weeks 2, 4, 6, and 8 after SNI, the distal nerve segment of the anastomotic site from 6 rats in the vehicle group and 6 rats in the GTPs group was fixed in glutaraldehyde buffer (pH 7.4, 0.1 mol/L) and 2% osmium tetroxide, dehydrated by a series of ethanol, and embedded in epoxy resin, successively. Thereafter, the 3-μm semi-thin sections 0.5 cm from the distal end of the nerve anastomosis were stained with toluidine blue, then the regenerated nerve fibers and myelin sheaths were observed. The images were observed under a light microscope (Carl Zeiss, Germany) and 5 random fields were photographed using a color digital camera (DC 300F). The total number of myelinated nerve fibers was counted.
TRANSMISSION ELECTRON MICROSCOPY OBSERVATION:
Ultrastructure of the regenerated nerves in SN was observed by transmission electron microscopy using the following protocol. In brief, at week 8 after SNI, samples from 6 rats in the vehicle group and 6 rats in the GTPs group were fixed in glutaraldehyde buffer (pH 7.4, 0.1 mol/L) and 2% osmium tetroxide successively, followed by dehydration with a series of ethanol, then the samples were embedded in epoxy resin. A Leica UC6 ultra-microtome was used to slice 70-nm ultrathin sections, which were stained by lead and uranium. Eventually, the slices were visualized with a HT 7700 TEM (HITACHI, Japan).
We measured the axonal diameter and myelin sheath thickness. The G-ratio was calculated with the followed equation: G-ratio=axonal diameter/axonal diameter+myelin sheath thickness×2.
RT-QPCR:
At week 8 after SNI, total RNA was extracted from SN stumps by TRIzol® (Thermo Fisher Scientific, Inc.). RNA concentration was measured by NanoDrop™ 2000 (Thermo Fisher Scientific, Inc.), followed by reverse-transcription into cDNA by PrimeScript RT Master Mix (Takara Bio, Inc., Otsu, Japan). qPCR was carried out using SYBR Premix Ex Taq (Takara Bio, Inc.) on a CFX96 (Bio-Rad Laboratories). GAPDH was used as an internal reference. Gene expression was analyzed by 2−ΔΔCq.
WESTERN BLOT:
At week 8 after SNI, SN stumps were lysed by radioimmunoprecipitation assay lysis buffer (Beyotime Biotechnology, Shanghai, China) supplemented with protease inhibitor (Sigma-Aldrich). The protein concentration was measured by bicinchoninic acid assay (Beyotime Biotechnology) and protein samples (15 μg/lane) were separated by 8% sodium dodecyl sulfate-polyacrylamide gel electrophoresis and transferred to polyvinylidene fluoride membranes (Millipore). The membranes were blocked by 5% non-fat milk before incubation with primary antibodies against NGF, GAP-43, NF200, MAG, and GAPDH at 4°C overnight and goat-anti-rabbit peroxidase-conjugated secondary antibody at room temperature for 2 h. Protein bands were visualized by enhanced chemiluminescence detection reagents (Thermo Fisher Scientific, Inc). GAPDH was used as a loading control.
STATISTICAL ANALYSIS:
Statistical analyses were carried out using SPSS 17.0 (SPSS Software, IBM, USA). Results are expressed as means±standard deviation (SD). Statistical comparisons between 2 groups were performed using the unpaired
Results
GENERAL SITUATION OF RATS AFTER SNI:
At week 2 after establishment of the SNI model, 30 rats in the vehicle group and 30 rats in the GTPs group exhibited varying degrees of foot/ankle swelling, gait instability, and foot dragging. In addition, in the vehicle group, 3 cases of plantar ulcer occurred, which healed at week 7 after SNI, with an obvious scar. However, in the GTPs group, only 1 case of plantar ulcer occurred, and the ulcer healed at week 4 after SNI, with a mild scar.
NEUROLOGICAL OBSERVATION:
At week 8 after the establishment of SNI, in 6 rats of the vehicle group the SN was hard and extensively adhered to the surrounding tissues, and there were few nutrient vessels on the nerve surface (Figure 1A). However, the 6 rats in the GTPs group had better flexibility and toughness of the SN, less adhesion to the surrounding soft tissues, and many more nutrient vessels were found on the surface (Figure 1B). In summary, the adhesion between nerve anastomosis and surrounding tissues of rats in the GTPs group was not as serious as in the vehicle group.
MEASUREMENT OF NERVE CONDUCTION VELOCITY:
At weeks 2, 4, 6, 8, and 12 after SNI, the mean conduction velocity of SN was measured in the vehicle group (n=6) and GTPs group (n=6) (Figure 2). At weeks 2, 4, 6, and 8 after SNI, the mean nerve conduction velocity in the GTPs group was significantly higher than that in the vehicle group (P<0.01, Table 1), while at week 12 after SNI, there was no significant difference in nerve conduction velocity between the vehicle group and GTPs group (P>0.05, Table 1).
MEASUREMENT OF WET TRICEPS WEIGHT AND MUSCLE FIBER AREA:
At weeks 4, 8, and 12 after SNI, the muscle recovery rate in the GTPs group was significantly higher than that of the vehicle group (P<0.01, Table 2).
NUMBER OF MYELINATED NERVE FIBERS:
At week 8 after the establishment of SNI, in the vehicle group (n=6) the morphology of nerve tissue was poor, the main type of regenerated nerve fiber was small-diameter myelinated fiber, the arrangement of myelin sheath was not regular, the maturity of myelin sheath and axon was somewhat poor, the number and density of myelin sheath and axon were low, and the proliferation of connective tissue was high (Figure 3A). Compared with the vehicle group, the arrangement of regenerated myelinated nerve fibers was more compact, neater, and denser, the diameter of regenerated nerve fibers was larger, and the proliferation of connective tissue was less in the GTPs group (n=6) (Figure 3B).
In addition, the number of myelinated nerve fibers in the GTPs group was significantly higher than that in the vehicle group at weeks 2, 4, 6, and 8 after SNI (P<0.01, Table 3), while no significant difference was observed between the vehicle group and GTPs group at week 12 after SNI (P>0.05, Table 3).
ULTRASTRUCTURE OF REGENERATED NERVES:
At week 8 after the establishment of SNI, in the vehicle group (n=6) the nerve was mainly composed of small and medium-sized myelinated nerve fibers, with sparse, thin, uneven thickness and orderly arrangement of the myelin sheath (Figure 4A). In the GTPs group (n=6) well-developed myelinated nerve fibers occurred, with clear structure, distinct layers, and regular/tight arrangement of myelin sheaths, while the regenerated nerve fibers were slightly uneven in thickness, thin in myelin sheath, and had a moderate number of unmyelinated nerve fibers (Figure 4B). In addition, the corresponding axonal diameter was larger (P<0.001), the myelin sheath was thicker (P<0.001), and the G-ratio was smaller (P<0.05) in the GTPs group than in the vehicle group (Table 4). These results show that nerve regeneration in the GTPS group was significantly better than in the vehicle group.
UNDERLYING MOLECULES IN SN STUMPS:
At week 8 after the establishment of SNI, expression of NGF, GAP-43, NF200, and MAG in SN stumps was significantly higher in the GTPs group (n=6) than in the vehicle group (n=6) (Figure 5A–5C).
Discussion
PNI accounts for approximately 1.5–4.0% of the world’s annual new trauma cases [1]. Many drug-based treatments have been explored for PNI repair. For instance, 4-AP promotes recovery of acute PNI and myelin regeneration in rats [2], vitamin supplements are beneficial for nerve regeneration in acute PNI [5], genistein is an adjuvant therapy for PNI [11], and these effects may be related to changes in estrogen level [12]. However, adverse effects exist, and there is an urgent need to find a convenient and accessible treatment without adverse effects.
GTPs in green tea exhibit protective effects in the CNS. For instance, GTPs prevent brain degenerative diseases [9,13,14] and cerebral ischemic diseases [15]. In addition, GTPs reduce the immune response and injury of transplanted PN in rats [16]; and (−)-epigallocatechin gallate (EGCG) in GTPs improves the survival of motor neurons after PNI [17]. The effects of GTPs on the PNS have not been previously investigated, and the present study aimed to determine whether GTPs can promote nerve regeneration in rats after PNI. The concentration of GTPs was first explored prior to performing the present study. Low and medium doses of GTPs are beneficial for hepatotoxicity and nephrotoxicity [18], while high doses of GTPs cause hepatotoxicity [19], which agrees with our initial preliminary work (data not shown) in which 3 doses of GTPs were tested: 50 mg/kg/d, 100 mg/kg/d, and 200 mg/kg/d. However, 1 rat died in the 100 mg/kg/d dosage group, and all rats died in the 200 mg/kg/d dosage group, due to respiratory tract disease, digestive tract disease, and eye congestion. All rats in the 50 mg/kg/d dosage group survived; thus, it was chosen for use in the subsequent experiments.
GTPs not only reduces lymphocyte production of pro-inflammatory cytokines, but also reduces inflammation around trauma [7]. Overexpression of inflammatory mediators in osteoarthritis can be inhibited by EGCG in GTPs [20]. GTPs also increase the production of vascular endothelial factors [21]. The present study found less adhesion between nerves and surrounding tissues at anastomotic stoma in the GTPs group than in the vehicle group, which may be due to the anti-inflammatory effects of GTPs; additionally, GTPs promote the regeneration of blood vessels around the injury, which may be responsible for the abundant capillaries around the nerve anastomosis. The slight inflammation in nerve anastomosis in the GTPs group may be related to the anti-inflammation effects of GTPs [22–24].
GTPs not only reduce blood sugar and lipids by inhibiting appetite and nutrient absorption, but also participate in lipid metabolism by regulating glycogen and lipid synthesis enzymes in the liver [25]. Furthermore, it can even change the expression of obesity genes of rats [26]. Nerve regeneration after PNI depends on recovery of limb function, and the nerve growth rate is a key factor affecting muscular atrophy [2]. In the present study the weight gain was slower and the recovery rate of wet triceps weight and nerve conduction velocity were faster in the GTPs group, indicating that GTPs stimulate nerves, promote the recovery from muscle atrophy, and improve the activity of affected limbs, despite its inhibitory effects on appetite and fat synthesis in rats.
Cells that function in nerve regeneration attracted our attention. Schwann cells (SCs) are precursor cells with reversible differentiation and different morphologies/functions, consisting of myelin- and non-myelin-forming cells [27]. In addition, SCs synthesize and secrete various NGF, neurotrophic factor (NTF), nerve cell adhesion factor (NCAF), and basement membrane adhesion proteins [28,29]. SCs play an important role in nerve regeneration [30]. For instance, at the axotomy of the CNS, most axons of the implanted SCs grow rapidly into the distal nerve of the graft, whose growth direction is consistent with the arrangement of SCs [31]. The present study found that nerve recovery in the GTPs group was much faster than that in the vehicle group, regardless of the number of myelinated nerve fibers, thickness of the myelin sheath, and morphology of SCs. The underlying mechanisms responsible for the effects of GTPs remain to be investigated. GAP-43 is a specific protein expressed during nerve regeneration and its high expression is associated with active nerve regeneration [32]. As one of the 6 growth factors, NGF functions in the survival and differentiation of neurons in the CNS [33] and its expression is increased in Schwann cells during nerve regeneration [34]. MAG is involved in the formation and maintenance of myelin [35], and NF200 is a marker of myelinated neurons [36]. The expression of NGF, GAP-43, NF200, and MAG in SN stumps was observed to be higher in the GTPs group than in the vehicle group.
Interestingly, there are also other agents applied for treatment of PNI. For instance, quercetin induces neurite growth by promoting GAP-43 expression [37], and isoquercitrin promotes peripheral nerve regeneration and remyelination after sciatic crush injury in mice [38]. The effects of GTPs on peripheral nerve regeneration and remyelination are similar to those of isoquercitrin.
In rats with SNI, GTPs relieved the adhesion between nerve anastomosis and surrounding tissues and improved the muscle recovery rate. At weeks 2, 4, 6, and 8 after SNI, the mean nerve conduction velocity and the number of myelinated nerve fibers in the GTPs group were higher than those in the vehicle group, while there was no significant difference at week 12 after SNI, which suggests that SN regeneration had occurred by week 12 after SNI in rats, and this effect warrants further study.
Conclusions
The present study demonstrated that GTPs promote recovery from PNI.
Figures
Figure 1. Neurological morphology of SN. The adhesion between nerve anastomosis and surrounding tissues in vehicle group (A) and GTPs group (B) (n=6). Figure 2. Conduction velocity of SN. At weeks 2, 4, 6, 8, and 12 after SNI, the mean conduction velocity of SN in vehicle group (A) and GTPs group (B) was measured by CM6240 physiological signal acquisition and processing system (n=6). Figure 3. Transverse section of SN. The regenerated nerve fibers and myelin sheaths in vehicle group (A) and GTPs group (B) were measured by optical microscopy (n=6). Figure 4. Ultrastructure of regenerated nerves in SN. The regenerated nerves in vehicle group (A) and GTPs group (B) were tested by a transmission electron microscopy (n=6). Figure 5. Underlying molecules in SN stumps. Expression of NGF, GAP-43, NF200, and MAG in SN stumps in vehicle group and GTPs group (A–C) was measured by RT-qPCR and Western blot (n=6). P<0.01, GTPs group vs. vehicle group.Tables
Table 1. Nerve conduction velocity at week 2, 4, 6, 8 and 12 after SNI (n=6). Table 2. The recovery rate of wet triceps weight at week 4, 8, 12 after SNI (n=6). Table 3. Number of myelinated nerve fibers at week 2, 4, 6, 8 and 12 after SNI (n=6). Table 4. Ultrastructure of regenerated nerves at week 8 after SNI (n=6).References
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