Detecting dopaminergic neuronal degeneration using diffusion tensor imaging in a rotenone-induced rat model of Parkinson’s disease: fractional anisotropy and mean diffusivity values

Lan-xiang Liu, Dan Du Tao Zheng Yuan Fang Yan-sheng Chen Hui-ling Yi Qing-yuan He, Da-wei Gao, Qing-lei Shi

1 Department of Magnetic Resonance Imaging, First Hospital of Qinhuangdao, Qinhuangdao, Hebei Province, China

2 Department of Radiology, Peking University Tird Hospital, Beijing, China

3 College of Environmental and Chemical Engineering, Yanshan University, Qinhuangdao, Hebei Province, China

4 Scientific Clinical Specialist, Siemens Ltd., Beijing, China

RESEARCH ARTICLE

Detecting dopaminergic neuronal degeneration using diffusion tensor imaging in a rotenone-induced rat model of Parkinson’s disease: fractional anisotropy and mean diffusivity values

Lan-xiang Liu1,＊, Dan Du1, Tao Zheng1, Yuan Fang1, Yan-sheng Chen1, Hui-ling Yi1, Qing-yuan He2, Da-wei Gao3, Qing-lei Shi4

1 Department of Magnetic Resonance Imaging, First Hospital of Qinhuangdao, Qinhuangdao, Hebei Province, China

2 Department of Radiology, Peking University Tird Hospital, Beijing, China

3 College of Environmental and Chemical Engineering, Yanshan University, Qinhuangdao, Hebei Province, China

4 Scientific Clinical Specialist, Siemens Ltd., Beijing, China

Graphical Abstract

Detecting dopaminergic neuronal degeneration using diffusion tensor imaging in a rotenone-induced rat model of Parkinson’s disease

Abstract

Dopamine content in the basal ganglia is strongly associated with the degree of dopaminergic neuron loss in the substantia nigra pars compacta. Symptoms of Parkinson’s disease might not arise until more than 50% of the substantia nigra pars compacta is lost and the dopamine content in the basal ganglia is reduced by more than 80%. Greater diagnostic sensitivity and specificity would allow earlier detection of Parkinson’s disease. Diffusion tensor imaging is a recently developed magnetic resonance imaging technique that measures mean diffusivity and fractional anisotropy, and responds to changes in brain microstructure. When the microscopic barrier (including cell membranes,microtubules and other structures that interfere with the free diffusion of water) is destroyed and extracellular fluid volume accumulates,the mean diffusivity value increases; when the integrity of the microstructure (such as myelin) is destroyed, fractional anisotropy value decreases. However, there is no consensus as to whether these changes can reflect the early pathological alterations in Parkinson’s disease.Here, we established a rat model of Parkinson’s disease by injecting rotenone (or sunflower oil in controls) into the right substantia nigra.Diffusion tensor imaging results revealed that in the stages of disease, at 1, 2, 4, and 6 weeks after rotenone injection, fractional anisotropy value decreased, but mean diffusivity values increased in the right substantia nigra in the experimental group. Fractional anisotropy values were lower at 4 weeks than at 6 weeks in the right substantia nigra of rats from the experimental group. Mean diffusivity values were markedly greater at 1 week than at 6 weeks in the right corpus striatum of rats from the experimental group. Tese findings suggest that mean diffusivity and fractional anisotropy values in the brain of rat models of Parkinson’s disease 4 weeks after model establishment can reflect early degeneration of dopaminergic neurons. Te change in fractional anisotropy values after destruction of myelin integrity is likely to be of greater early diagnostic significance than the change in mean diffusivity values.

Key Words:nerve regeneration; diffusion tensor imaging; fractional anisotropy; mean diffusivity; magnetic resonance imaging; Parkinson’s disease; rotenone; neurodegenerative disease; biomarkers; substantia nigra; tyrosine hydroxylase; neural regeneration

Introduction

Parkinson’s disease (PD) is a progressive neurodegenerative disease that is becoming increasingly prevalent in young people (Mehanna et al., 2015). Its symptoms arise late in the disease stage, and it is often dif ficult to distinguish from other neurodegenerative diseases (Tanawattano et al., 2015). It is important to identify PD early and begin treatment as early as possible to obtain a good prognosis (Long et al., 2012;Gazewood et al., 2013; Liang et al., 2015).

Over the past two decades, a variety of imaging techniques have been used to search for biomarkers of PD. The most common approach in magnetic resonance imaging (MRI) is voxel-based morphometry, which is used to evaluate atrophy in cortical and subcortical structures. However, voxel-based morphometry cannot be reliably used to diagnose PD (Burton et al., 2004; Ramirez-Ruiz et al., 2005; Feldmann et al.,2008; Benninger et al., 2009; Ibarretxe-Bilbao et al., 2010).Another type of imaging, proton magnetic resonance spectroscopy, demonstrated a reduction in the N-acetylaspartate/choline ratio in the lentiform nucleus of patients with PD,and an asymmetric decrease in N-acetylaspartate/creatinine ratio in the contralateral substantia nigra in patients with PD with unilateral symptoms. However, the diagnostic ef ficiency of this technique remains to be confirmed in further clinical experiments using strong magnetic fields (Choe et al., 1998;Clarke et al., 2000; de Celis Alonso et al., 2015). Other MRI techniques include diffusion-weighted imaging and magnetization transfer imaging; however, to date, none of these techniques have reached the accuracy and reliability required to justify their introduction into standard clinical practice or as part of interventional clinical trials. Particularly promising results have been obtained with diffusion tensor imaging(DTI) used to investigate the diffusion characteristics of the substantia nigra.

DTI can assess the random movement of protons of water molecules in terms of overall extent (mean diffusivity, MD)and orientational dependence (fractional anisotropy, FA)(Tak et al., 2016). Te correlation between dopaminergic cell loss in the substantia nigra and the progressive symptoms of PD makes imaging of the substantia nigra a promising noninvasive method of examining patients with PD. Indeed,a narrowing of signals from the pars compacta of the substantia nigra was found in patients with PD (Duguid et al.,1986; Atasoy et al., 2004; Sohmiya et al., 2004). Te loss of dopaminergic neurons removes diffusion barriers and their orientational dependence, which results in greater diffusivity and lower anisotropy, as demonstrated in a number of neurodegenerative diseases (Le Bihan, 1995; Abe et al., 2002;Hikishima, 2015). Te DTI value has been validated for the diagnosis of PD, and negative or positive relationships between FA or MD values, as well as the degeneration of the nigrostriatal pathway, have been found (Brooks, 1995; Chesselet et al., 1996; Booij et al., 1997; Vaillancourt et al., 2009;Lewis et al., 2009; Zhan et al., 2012). Despite this, pathological data from patients in clinical trials cannot be obtained in most situations. Therefore, studying the pathogenesis,early diagnosis and treatment of PD in an established animal model remains important for obtaining pathological results.

Rotenone is a natural, fat-soluble compound extracted fromDerris elliptica. It readily traverses cell membranes and the blood-brain barrier, without the aid of the dopamine transporter. Rotenone can specifically suppress the activity of mitochondrial complex I, which leads to the failure of oxygen utilization and energy metabolism (Friedrich et al.,1994; Qiu et al., 2016). Previous studies have reported that rotenone injected into rats can selectively damage the mesolimbic dopamine system, resulting in a successful model of PD by reproducing Lewy body development and disease progression in rats (Shiman et al., 1971; Betarbet et al., 2000;Ryu et al., 2002; Sherer et al., 2003; Tayarani-Binazir et al.,2010; Duty and Jenner, 2011; Voitenko and Nikonenko, et al., 2015). Optimal time points for such measurements have also been suggested, but are not consistent (Van Camp et al.,2009; Delli Pizzi et al., 2013).

Furthermore, decreasing neurotransmitter levels in the nigrostriatal pathway has been suggested as one of the main mechanisms of inducing PD (Tayarani-Binazir et al., 2010).Tyrosine hydroxylase (TH) is the rate-limiting enzyme in the synthesis of catecholamines and plays an important role in dopamine biosynthesis. Te activity and expression of TH in striatal pathways can therefore directly affect the biosynthesis of dopamine. Therefore, variations in TH are strongly associated with the occurrence and development of PD (Valente,2001). In patients with PD, as well as in rat models of the disease, TH shows abnormal expression and activity, from gene to enzyme (Lücking, 2000). In addition, α-synuclein, a protein discovered recently that is strongly associated with PD, is also the essential component of Lewy bodies. Although the mode of action of α-synuclein is still unclear, this protein can suppress the expression and activity of TH (Yu et al., 2004).Terefore, the level and activity of TH can be used as a biomarker for determining the success of animal models of PD.

The aims of the present study were to determine the diagnostic accuracy of DTI in a rotenone-induced rat model of PD, and to identify the optimal measurement time point using immunohistochemistry.

Materials and Methods

Animals

Tirty adult male specific-pathogen-free Sprague Dawley rats,aged 2–3 months and weighing 180–310 g, were provided by Beijing HFK Bioscience, China (animal approval No. SCXK(Jing) 2009-0004). Te rats were fed a rodent chow and purified water, and were housed under standard conditions. All procedures and housing conditions followed international ethical statutes and laws for the protection of animals, and were approved by the Animal Ethics Committee of First Hospital of Qinhuangdao, China (approval No. 20140018).

PD model establishment

Te rats were randomly allocated to two groups (control,n=6; experimental,n= 24). All rats were anesthetized with an intraperitoneal injection of 0.6 mL pentobarbital (Cat. No.P8410; 0.3%; Solarbio, Beijing, China) and placed in a ste-reotaxic frame. Te injection position for the right substantia nigra was determined using the following stereotaxic coordinates from bregma: anteroposterior, −4.8 mm; mediolateral,1.9 mm; dorsoventral, −7.8 mm (Figure 1). Rats in the control group received an injection of 2 μL sunflower oil, and those in the experimental group received 3 μg rotenone (No.R8875-1G) dissolved in 2 μL dimethyl sulfoxide. Twelve rats died from intolerance to anesthesia or hemorrhage during injection, leaving 12 in the experimental group.

Figure 1 Parkinson’s disease model establishment: rotenone injection into the substantia nigra.

Figure 2 Coronal imaging of mouse brain.

Figure 3 Coronal T2-weighted images showing selection of regions of interest.

Figure 4 Tyrosine hydroxylase (TH)immunohistochemistry in the substantia nigra 6 weeks after rotenone injection (light microscopy).

Rats in the experimental group showed rotational behavior 10 minutes after apomorphine (0.25 mg/kg intraperitoneally)was administered, 1, 2, 4, and 6 weeks after surgery (Sindhu,et al., 2005) and the number of rotations was counted within 30 minutes. A rotational speed greater than 7 rotations/minute indicated the model had been established successfully.

MR image acquisition and post-processing

At 1, 2, 4, and 6 weeks after surgery, all 18 rats were anes-thetized with pentobarbital (0.6 mL intraperitoneally) and placed onto temperature-controlled animal beds in a 3.0 Tesla MRI scanner (Magnetom Verior; Siemens, Erlangen,Germany) with a 4-channel, 50 mm diameter phased array animal coil (part number: 10-F04885). Te imaging protocol comprised coronal (cT2WI) and transverse (tT2WI) wholebrain T2-weighted imaging, and coronal (c)DTI. Te cT2WI and cDTI sequences had identical slice thickness, slice gap and slice number and were located at the same level of the substantia nigra. The anatomical structures of the corpus striatum, midbrain and most of the medulla were included in cT2WI and cDTI image acquisition.

MRI parameters were as follows: cT2WI turbo spin echo(repetition time/echo time = 3,000/113 ms, flip angle = 150°,field of view = 74 mm × 74 mm, average = 14, voxel size = 0.3 mm × 0.3 mm × 2.0 mm, slice thickness = 2.0 mm, number of slices = 10); tT2WI turbo spin echo (repetition time/echo time = 4,000/111 ms, flip angle = 150°, average = 10, field of view = 70 mm × 70 mm, voxel size = 0.4 mm × 0.3 mm × 2.0 mm, slice thickness = 2.0 mm, number of slices = 12). With the same slice orientation and position as cT2WI, single-shot echo-planar imaging was used in DTI and the settings were as follows: repetition time/echo time = 1,800/110 ms, field of view = 74 mm × 74 mm, slice thickness = 2 mm, voxel size= 1.5 mm × 1.0 mm × 2.0 mm, sensitivity encoding factor =2, nonlinear directions = 15,b-value = 0/1,000 s/mm2. To increase the signal-to-noise ratio, scanning was repeated nine times (total scanning time = 17 minutes, 38 seconds).

Imaging analysis was carried out using prototype software on a workstation (Siemens Verio 3.0 T MR Leonardo 3682).MD and FA maps of mouse brains were compared with coronal T2WI slices (Figure 2). One radiologist with 10 years of experience in neural MRI, who was blinded to experimental grouping, placed circular regions of interest (ROI) measuring 0.30–0.60 cm2in the center of the substantia nigra and in the head, body, and tail sub-regions of the corpus striatum on both sides (Figure 3). To increase the accuracy of the measured values, freehand ROIs were carefully matched to the margins of the corpus striatum and the substantia nigra,first using cT2WI images as reference images and then copying them to corresponding parameter maps. Te final values for the corpus striatum and substantia nigra were calculated from, respectively, the average values of the three sub-regions of the corpus striatum and the mean parameters of the substantia nigra.

Immunohistochemistry

After MRI at 6 weeks, rats were killed by decapitation under deep anesthesia using 0.6 mL pentobarbital (Solarbio,Beijing, China). Coronal sections (15 μm thickness) were cut using a cryostat and mounted in paraffin. Brain sections were incubated overnight at 4°C with rabbit anti-rat TH antibody (1:300; Abcam, Cambridge, UK), followed by horseradish peroxidase-conjugated goat anti-mouse IgG (SP-9001; Beijing Zhongshan Golden Bridge Biotechnology, Beijing, China) for 30 minutes at 37°C. 3,3′-Diaminobenzidine was used for visualization. Lastly, all tissue specimens were stained with hematoxylin and eosin and viewed under a light microscope (Olympus, Tokyo, Japan) equipped with a CCD camera (Leica DMI4000B, Germany). Neuronal changes(shape of TH-immunoreactive cells and the level of cytoplasm staining in the substantia nigra) were examined by a pathologist with 30 years of experience in neuropathological examination.

Statistical analysis

Statistical comparisons were performed using SPSS 16.0 soft-ware (SPSS, Chicago, IL, USA). All data are presented as the mean ± SD. A two samplet-test was used to test the difference in FA and MD values in the substantia nigra and corpus striatum between the control and experimental groups on both sides. Comparisons between every time point of FA and MD were analyzed using repeated measures analysis of variance and the Bonferroni test. The null hypothesis (the error covariance matrix of the orthonormalized transformed dependent variables is proportional to an identity matrix)was tested using Mauchly’s test of sphericity. The Greenhouse-Geisser method was used to adjust the degrees of freedom for the average tests of significance.P＜ 0.05 was considered statistically significant.

Results

Comparison of FA and MD values between control and experimental groups after combining data at all time points

When the data from all four time points were combined, the FA value in the right substantia nigra was 26.75% (F= 20.64,P＜ 0.001) lower in the experimental group than in the control group, and the MD value was 24.51% (F= 8.16,P= 0.01)greater than that in the control group. Tere were no significant differences in FA or MD values between experimental and control groups on either side of the corpus striatum, or in the FA value in the left substantia nigra, when data from all time points were combined (Table 1). Repeated measures analysis of variance revealed no significant trend over time,and no interaction between time and group for the FA and MD values in either region (P＞ 0.05).

FA and MD values for the substantia nigra and corpus striatum on both sides in the experimental group

In the experimental group, FA values in the right substantia nigra were lower at 4 weeks than at 1, 2, and 6 weeks, with a significant difference between 4 and 6 weeks. MD values in the right corpus striatum were higher at 1 week than 2, 4 and 6 weeks, with a significant difference between 1 and 6 weeks(P＜ 0.05;Table 2). No significant differences were found for FA and MD values on the left side of the substantia nigra or corpus striatum.

Comparisons of the FA and MD values between the control and experimental groups at each time point

Right substantia nigra FA values were significantly lower in the experimental group than in the control group at different time points. MD values in the experimental group were sig-nificantly higher than in the control group in the first subgroup (P＜ 0.05;Table 2).

Immunohistochemistry results

Te right substantia nigra of the experimental group showed changes in neuronal morphology and nuclear condensation.In addition, there were fewer TH-immunopositive cells, and the cytoplasm was less strongly stained, in the experimental group than in the control group. Tere were no notable observations on the left side or in the control group (Figure 4).

Table 2 Comparison of fractional anisotropy and mean diffusivity values between control and experimental groups at 1–6 weeks after model establishment

Table 1 Fractional anisotropy and mean diffusivity values derived from DTI between control and experimental groups (combined time points)

Discussion

MRI can provide important informationin vivo, allowing the examination of cortical or subcortical regions in patients with PD. However, conventional MRI techniques can only provide limited information for diagnosis and therapeutic monitoring, and are mainly used to discriminate PD from atypical syndromes, exclude secondary features such as vascular lesions, and confirm the absence of specific imaging features found in atypical parkinsonism. High-field DTI has been reported to detect regional and specific alterations in the microscopic integrity of the white matter and basal ganglia known to be involved in PD pathology (Baglieri et al., 2013). Significant correlations between the alteration of DTI-derived parameters in the putamen, and other regions affected in PD, were also found in the context of PD subtypes. Therefore, microstructural alterations detected with high field DTI could be used as biomarkers for the diagnosis and monitoring of PD (Zhan et al., 2012).

Here, we evaluated the feasibility of using FA and MD values for diagnosing PD in rotenone-induced rat models, and examined the corresponding morphological characteristics.When the data from all time points were combined, lower FA values and higher MD values were observed in the right substantia nigra in the experimental group than in the left substantia nigra or control group. The reason for this may be a degeneration of dopaminergic neurons and an increase in water content in the PD models. Additionally, after multivariate analysis of FA values in the right substantia nigra,significant differences were detected between the control and experimental groups at various time points, whereas for MD values only the first week showed a significant difference between groups. This suggests that FA values are a more sensitive measure of dopaminergic neuronal degeneration than MD values. Moreover, FA values in the right substantia nigra in the experimental group were lower at 4 weeks than at 1, 2, and 6 weeks, with a significant difference between 4 and 6 weeks. Te reason for this may be that degeneration of dopaminergic neurons is more advanced, suggesting that this is the optimal time point at which to measure effects in rotenone-induced PD rat models on the experimental side.

Tese findings were in agreement with the literature investigating the role of DTI-derived parameters in PD rat models. For example, Boska et al. (2007) reported that the MD value increased and the FA value decreased in the substantia nigra in rats 5–7 days after PD model establishment using1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine, and this was validated using histochemistry. Furthermore, Boska’s study demonstrated that the FA value in the right substantia nigra was lowest at 4 weeks, but increased at 6 weeks, nearly reaching the original level. Te reason for this may be gliosis and inflammation of the nuclei, or intrusion of surrounding fibers into the shrinking structure (Rosas et al., 2006; Guo et al., 2015; Lenfeldt et al., 2015). It might also be due to a decrease in anisotropy of the molecular microstructure in the early stages (1–4 weeks) that was restored at a later stage (6 weeks). Similarly, other than the changes in water diffusion in the right substantia nigra, the changes in MD in weeks 1–6 in the right substantia nigra in the experimental group might also be caused by the same factors. Changes in MD value, a DTI-derived parameter, in the right corpus striatum and other anatomical structures indicated secondary damage, which may have been causedviathe cortico-striato-nigral pathway. Tis pathway comprises fiber connections between the substantia nigra, corpus striatum and putamen,as confirmed by neuroanatomy and pathology (Blackwell et al., 2003).

However, our results differ from those reported by Van Camp et al. (2009), in which FA values in the ipsilateral substantia nigra were elevated. Tis might be due to differences in protocol between the present study and theirs. First, in their experiment, 6-hydroxydopamine was used to produce the model.Tis would cause the production of free radicals, which would attack the cell membrane and lead to over-oxidation. Secondly,the injection volume in their experiment was 4 μL, whereas we used 2 μL. Tis difference may have affected the degeneration of the nigrostriatal pathway (Przedborski et al., 1995; Ferro et al., 2005; Kondoh et al., 2005). Tird, the anatomical structure into which they injected 6-hydroxydopamine was the corpus striatum, whereas we injected our rats in the substantia nigra.All these factors may have caused the differences between Van Camp et al.’s experiment and ours.

Histologically, we observed fewer TH-immunopositive cells and less cytoplasmic staining in our experimental animals than in the control animals, and pyknosis occurred.These changes indicate the destruction of dopaminergic neurons in the substantia nigra, confirming our model was established successfully. Terefore, it seems that the FA and MD values reflect the neuronal damage in the PD model,suggesting they are promising biomarkers in the diagnosis and therapeutic monitoring of the disease.

Our study has some limitations. First, the sample size was small; future studies with large samples should be conducted to determine the reproducibility of the results. Second,due to limited experimental conditions, the substantia nigra could not be measured separately. Tird, all ROIs were determined manually for the DTI, which might have given rise to measurement error in the FA and MD calculations. However, as MRI and post-processing techniques are developed,DTI will certainly play an increasingly important role in the diagnosis and monitoring of PD.

In summary, the DTI-derived parameters FA and MD provide valuable information for the detection of dopaminergic neuron damage in a rotenone-induced rat model of PD. Te FA value seems to be more sensitive to dopaminergic neuron damage than the MD value. In addition, our results suggest that 4 weeks after rotenone administration may be the optimal time point for measuring DTI parameters in rat models.

Acknowledgments:We thank Dr. Hong-bin Han from Beijing Key Laboratory of Magnetic Resonance Imaging Device and Technique for his generous technical help. We would like to thank Dr. Min Zhao and Fang Xiao from Department of Pathology, First Hospital of Qinhuangdao for their technical instructions in immunohistochemistry.

Author contributions:LXL, YF, DD, and QYH designed this study. DD and TZ performed experiments. DD, YSC, HLY, and QLS analyzed data.DD and DWG wrote the paper. All authors approved the ?nal version of the paper.

Conflicts of interest:None declared.

Research ethics:Te study protocol was approved by the Animal Ethics Committee of First Hospital of Qinhuangdao (approval No. 20140018).Te experimental procedure followed the United States National Institutes of Health Guide for the Care and Use of Laboratory Animals (NIH Publication No. 85-23, revised 1986).

Data sharing statement:Te datasets analyzed during the current study are available from the corresponding author on reasonable request.

Plagiarism check:Checked twice by iTenticate.

Peer review:Externally peer reviewed.

Open access statement:Tis is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.

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Copyedited by Slone-Murphy J, Maxwell R, Wang J, Li CH, Qiu Y, Song LP,Zhao M

How to cite this article: Liu LX, Du D, Zheng T, Fang Y, Chen YS, Yi HL, He QY, Gao DW, Shi QL (2017) Detecting dopaminergic neuronal degeneration using diffusion tensor imaging in a rotenone-induced rat model of Parkinson’s disease: fractional anisotropy and mean diffusivity values. Neural Regen Res 12(9):1485-1491.

Funding: This work was financially supported by the Research Grant of Hebei Province Science and Technology Project of China, No.1427777118D.

＊Correspondence to:Lan-xiang Liu,liulanxiang66@sina.com.

orcid:0000-0002-7434-4434(Lan-xiang Liu)

10.4103/1673-5374.213559

Accepted: 2017-06-03