Normalization of ventral tegmental area structure following ... : Neural Regeneration Research (original) (raw)
Introduction
Opioid drugs, such as heroin, are addictive and can produce physical and psychological dependence after use. Heroin abuse can damage many brain areas, including the pedunculopontine tegmental nucleus of the midbrain, the ventral tegmental area, and nucleus accumbens[12]. The ventral tegmental area contains dopamine neurons involved in the meso-limbic dopamine system, and along with the nucleus accumbens, are the main brain regions associated with the reward pathway[1]. Rodd et al.[3] found that local injection of 5-hydroxytryptamine receptor agonist in mouse ventral tegmental area could increase the activity of dopamine neurons. Interestingly, injection of 5-hydroxytryptamine receptor antagonist in the posterior lobe of the ventral tegmental area could suppress alcohol and cocaine addiction[3]. Our previous study demonstrated that neuronal degeneration and swelling were evident in the prefrontal lobe cortex and nucleus accumbens of rats with heroin relapse[4]. These results indicated that persistent use or one large-dose of heroin induced acute or chronic damage to the nervous system. The ventral tegmental area-nucleus accumbens pathway is a site where all addictive drugs produce acute reward effects[1]. Moreover, the ventral tegmental area is an essential region in the reward pathway, however our previous study neglected the ventral tegmental area. Thus, this study sought to observe the changes in neuronal ultrastructure in the ventral tegmental area during heroin relapse.
Heroin spongiform leukoencephalopathy is an organic brain disease occurring in white matter of the central nervous system from addicts who inhaled or injected heroin. This disease is characterized by the presence of spongy degeneration in the white matter[56789]. Recurrent drug use after heroin addiction may cause the occurrence of heroin spongiform leukoencephalopathy. Our previous studies[41011] concerning clinical and experimental research into heroin relapse verified that long-period large-dose use of heroin led to the alteration in brain morphology, such as changes in brain cell ultrastructure and brain imaging. Acupuncture treatment has been a feasible clinical intervention when heroin spongiform leukoencephalopathy occurs[12]. Acupuncture promotes the rehabilitation of brain injury, and protects and nourishes nerve cells in the central nervous system[13]. Nevertheless, at present, acupuncture has not been widely used to treat heroin addiction. Medicine, such as methadone, buprenorphine, and naltrexone, is still the first choice for detoxification in the clinic. Methadone, a typical μ opioid receptor agonist, lessens abstinence syndrome, and is extensively used in detoxification and maintenance therapy for heroin addiction in the clinic. Therefore, methadone is selected as a positive control. Brain-derived neurotrophic factor and glial cell line-derived neurotrophic factor are strongly associated with neuronal growth, development, differentiation, maturity, nervous system development, neuronal injury, and some diseases in the nervous system[1415161718]. Brain-derived neurotrophic factor and glial cell line-derived neurotrophic factor participate in nerve repair, contribute to nervous system development, activate neural pathways, and protect and repair injured neurons[1415161718]. A previous study suggested that acupuncture regulated neurotrophic factors after cerebral ischemia[12]. Following the occurrence of cerebral ischemia, apparently increased brain-derived neurotrophic factor protein expression significantly relieved ischemic brain injury (such as cerebral edema), and inhibited neuronal necrosis[19]. This study was designed to observe the structure of brain tissue, brain-derived neurotrophic factor and glial cell line-derived neurotrophic factor expression changes, and acupuncture effects in heroin relapse rats, and then to further investigate the precise mechanisms of acupuncture treatment for heroin-associated encephalopathy.
Results
Quantitative analysis of experimental animals
A total of 32 rats were randomly and equally divided into normal, model, acupuncture and methadone groups. A rat model of heroin relapse was established by narcotic use until addiction occurred, and then creating a detoxification process by withholding heroin from the model, acupuncture and methadone groups. Model rats in the acupuncture group received acupuncture at Baihui (DU20) and Dazhui (DU14) during the detoxification period. Rats in the methadone group were intragastrically administered a decreasing amount of methadone during the detoxification period. All rats were included in the final analysis.
Acupuncture improved neuronal ultrastructure of the ventral tegmental area in rats with heroin relapse
Electron microscopy showed clear nuclear membranes, normal rough endoplasmic reticulum, ribosomes and nuclei, abundant rough endoplasmic reticulum and mitochondria, and slightly expanded rough endoplasmic reticulum in the ventral tegmental area of rats in the normal group. In the model group, nuclear membrane boundaries were obscure, rough endoplasmic reticulum expansion was seen, along with vacuolar degeneration of some mitochondria in the ventral tegmental area, indicating that nerve cells were severely injured in rats with heroin relapse. In the methadone and acupuncture groups, nuclear membranes were visible, ribosomes and rough endoplasmic reticulum were abundant, rough endoplasmic reticulum was normal or lightly expanded, and a few mitochondria were vacuolar and degenerated in the ventral tegmental area. These results suggested that acupuncture protected nerve cells against injury in rats with heroin relapse. In addition, no major difference in neuronal ultrastructure was detected in the ventral tegmental area of heroin relapse rats between the methadone and acupuncture groups (Figure 1).
Acupuncture effects on the ultrastructure in the ventral tegmental area of heroin relapse rats (transmission electron microscopy, × 10,000).(A) Normal group: normal ribosomes, mitochondria and rough endoplasmic reticulum in the ventral tegmental area. Arrows show endoplasmic reticulum. (B) Model group: reduced number of ribosomes, decreased number of mitochondria, partial vacuolar degeneration, and expanded rough endoplasmic reticulum. Arrows show nuclear membranes and mitochondria. (C) Methadone group: clear nuclear membranes, abundant ribosomes and rough endoplasmic reticulum, and a few vacuolar mitochondria. Arrows show vacuolar mitochondria and ribosomes. (D) Acupuncture group: clear nuclear membranes, abundant uniform ribosomes, a few vacuolar mitochondria, and lightly expanded rough endoplasmic reticulum. Arrows show nuclear membranes and mitochondria.
Acupuncture increased brain-derived neurotrophic factor expression in the ventral tegmental area of heroin relapse rats
Immunohistochemical staining demonstrated that compared with the normal group, the number of brain-derived neurotrophic factor-positive cells and mean absorbance were greater in the ventral tegmental area of heroin relapse rats (P < 0.05). The number of brain-derived neurotrophic factor-positive cells and mean absorbance were increased after treatment with methadone or acupuncture (P < 0.05). The number of brain-derived neurotrophic factor-positive cells and mean absorbance were greater in the acupuncture group that those in the methadone group (P < 0.05; Figure 2, Table 1).
Acupuncture effects on brain-derived neurotrophic factor (BDNF) and glial cell line-derived neurotrophic factor (GDNF) expression in the ventral tegmental area of heroin relapse rats (immunohistochemical staining, × 20).Arrows show BDNF or GDNF expression. (A, E) Normal group: BDNF or GDNF expression was visible in the tissue. (B, F) Model group: BDNF or GDNF expression was increased after heroin relapse. In the methadone group (C, G) and acupuncture group (D, H), BDNF or GDNF expression was noticeably increased. Moreover, BDNF expression was greater in the acupuncture group than that in the methadone group.
Acupuncture effects on brain-derived neurotrophic factor (BDNF) and glial cell line-derived neurotrophic factor (GDNF) expression in the ventral tegmental area of heroin relapse rats
Acupuncture increased glial cell line-derived neurotrophic factor expression in the ventral tegmental area of heroin relapse rats
Immunohistochemical staining showed that compared with the normal group, the number of glial cell line-derived neurotrophic factor-positive cells and mean absorbance were greater in the ventral tegmental area of heroin relapse rats (P < 0.05). The number of glial cell line-derived neurotrophic factor-positive cells and mean absorbance were increased after treatment with methadone or acupuncture (P < 0.05). The number of glial cell line-derived neurotrophic factor-positive cells and mean absorbance were greater in the acupuncture group compared with the methadone group (P < 0.05; Figure 2, Table 1).
Discussion
Acupuncture at Baihui and Dazhui normalizes neuronal ultrastructure in the ventral tegmental area of heroin relapse rats. Acupuncture at Baihui and Dazhui also contributes to brain-derived neurotrophic factor and glial cell line-derived neurotrophic factor expression, and protects nerve cells against injury in heroin relapse rats. These results suggested that acupuncture had protective effects on nerve cells in the ventral tegmental area of heroin relapse rats at the levels of cell morphology and protein molecule expression.
Morphological alteration in injured brain induced by heroin and acupuncture
Numerous studies suggested that white matter injury and brain atrophy were detectable in the brain of heroin-dependent subjects[2021222324252627282930]. Relevant imaging examination also demonstrated that abnormal signal changes were detected in the white matter, cerebellar white matter, and posterior limb of the internal capsule of these subjects. Other studies confirmed that ultrastructural alterations were visible in the cerebral cortex, hypothalamus and pituitary gland of heroin-addicted rats, monkeys and humans[3031323334]. These findings suggest that extensive pathological lesions were detected in the brain of heroin-addicted rats, mainly present as neuronal degeneration and death, which gave a morphological reason behind the brain injury induced by relapse.
We have performed many studies on detoxification with acupuncture, and verified that acupuncture at Zusanli (ST36) could improve abstinence symptoms in morphine-addicted rats. Acupuncture lessened protracted abstinence symptoms in heroin-addicted persons during the rehabilitation period[35]. Acupuncture combined with psychological desensitization could improve sleep and anxiety disorders[36]. Magnetic resonance imaging and functional magnetic resonance imaging revealed that heroin could activate brain areas regulating craving-related reward, learning and memory, cognition and emotion, but acupuncture at Zusanli suppressed the activation of craving-related brain areas[1011]. Experimental studies confirmed that acupuncture improved neuronal ultrastructure in the prefrontal lobe cortex, hippocampus and nucleus accumbens of heroin relapse rats[373839]. These results indicated that acupuncture had a protective effect on the injured brain tissue of heroin relapse rats.
Given the findings described in the above studies, this study further continued research into the effect of heroin relapse on the brain by observing the alterations in ultrastructure of the ventral tegmental area in heroin relapse rats using electron microscopy. Our findings verified the morphological changes in injured brains after heroin relapse. After persistent treatment with acupuncture, the injury to nerve cells was improved, suggesting that acupuncture had a protective effect on injured nerve cells. The protective effects of acupuncture provide experimental evidence for clinical application of acupuncture.
Significance of studying the ventral tegmental area
The opioid-induced reward effect is a direct reason for opioid addiction[40]. A previous study showed that brain areas, such as the nucleus accumbens, ventral tegmental area, interior cortex of the frontal lobe, the pedunculopontine tegmental nucleus, hippocampus, hypothalamus, ventral globus pallidus and amygdale, were involved in the opioid-induced reward effect. These nuclear groups and their connecting structures were called the reward pathway[41].
There are two reward pathways involved in relapse addiction: the mesolimbic pathway (from the ventral tegmental area to the nucleus accumbens), and the mesocortical pathway (from the ventral tegmental area to the frontal cortex). The ventral tegmental area is an essential area in these two dopamine reward pathways, and contains numerous dopaminergic neurons. The release of dopamine from the ventral tegmental area produces the rewarding effect of heroin and induces abstinence symptoms during withdrawal. Thus, drug addicts experienced pleasant feelings and cognitive disorder. Therefore, the ventral tegmental area was selected as a reward pathway to observe morphological changes and the expression of neurotrophic factors under an electron microscope[41].
Owing to the complexity and integrity of the nervous system, various neurotransmitters, signal pathways and genes create a networked adjusting process during addiction and relapse. Studies addressing molecular mechanisms of addiction relapse mainly contained two aspects: (1) monoamine neurotransmitters and receptors such as dopamine, noradrenaline and 5-hydroxytryptamine. Most addictive drugs cause an increase in dopamine release in the nucleus accumbens dominated by dopaminergic neurons in the ventral tegmental area[42]. Dopamine acts on dopamine receptors and exerts an important effect on studies into learning and memory, especially when behaviors are related to reward. (2) Excitatory and inhibitory amino acids and their receptors. Glutamate and its receptors (mainly N-methyl-D-aspartate receptor and amino-3-hydroxy-5-isoxazolepropionic acid receptor) play an important role in neural plasticity of addiction. The nucleus accumbens is strongly associated with learning and memory-related structures such as the prefrontal cortex, hippocampus and amygdale, which possibly indirectly induce the formation of habitual memory via the dorsal striatum, regulates obsessive-compulsive behaviors and generates relapse[434445464748495051]. The present study investigated molecular mechanisms of heroin relapse from the angle of neurotrophic factor expression.
Neurotrophic factor expression and acupuncture
Glial cell line-derived neurotrophic factor has been shown to protect neurons against injury, and also contributes to axon growth[52]. These effects occur because glial cell line-derived neurotrophic factor bound to its α1 receptor, and then activated receptor tyrosine kinase[53]. Glial cell line-derived neurotrophic factor is the only neurotrophic factor that resists neuronal apoptosis and blocks cell atrophy[54]. Glial cell line-derived neurotrophic factor can enhance cell proliferative ability in the subventricular zone and subgranular zone of the hippocampal dentate gyrus, and exogenous glial cell line-derived neurotrophic factor accelerates the repair of nerve injury in the central nervous system[55].
Brain-derived neurotrophic factor promotes the growth, development, differentiation[56] and functional expression of nerve cells during the development of the central nervous system. Simultaneously, brain-derived neurotrophic factor maintained neuronal function in the central nervous system. Brain-derived neurotrophic factor promoted synaptic plasticity, altered neuronal morphology in the brain, increased the density of synaptic terminals and contributed to the outgrowth of dendrites and axons[14]. Moreover, brain-derived neurotrophic factor suppressed nociceptive stimulus and led to neuronal regeneration. Heroin-associated encephalopathy was closely correlated to learning and memory. Drug addiction and learning and memory processes occur in common anatomic structures in the central nervous system. Glutamate and dopamine receptor systems and their interactions regulate the formation and consolidation of addiction memory[57]. Chronic drug addiction increases the expression levels of mature brain-derived neurotrophic factor in the ventral tegmental area, which was associated with the dopamine system and reward circuit[15]. Vargas-Perez et al.[16] suggested that mature brain-derived neurotrophic factor directly participated in the switching mechanism of the ventral tegmental area, and changed reward circuits from non-dopamine-dependent into dopamine-dependent pathways. Rats have displayed drug addiction and withdrawal behaviors after mature brain-derived neurotrophic factor was injected into neurons in the ventral tegmental area. Luo et al.[16] confirmed that acupuncture at Dazhui and Baihui enhanced brain-derived neurotrophic factor expression in rats with focal cerebral ischemia, blocked intracellular Ca2+ overloading, and stabilized the intracellular environment.
These studies demonstrated that neurotrophic factors prevented the death of injured neurons, regulated synaptic plasticity, reduced neural degeneration, prevented disease progression, stimulated axon growth and promoted regeneration[1718]. This study showed that brain-derived neurotrophic factor and glial cell line-derived neurotrophic factor expression was increased in the rat frontal lobe and ventral tegmental area of heroin relapse rats, and indicated that chronic toxic effects of heroin caused nerve cell injury, led to compensatory protection of the body, increased endogenous brain-derived neurotrophic factor and glial cell line-derived neurotrophic factor expression, and repaired injured nerve cells. Results from this study verified that this kind of compensatory protection could not repair injured nerve cells, and its repair effects were far less than the nociceptive effects of chronic heroin. These findings were consistent with the results in the model group (brain-derived neurotrophic factor and glial cell line-derived neurotrophic factor expression was increased and cell structure was obviously damaged).
In the present study, an increased brain-derived neurotrophic factor and glial cell line-derived neurotrophic factor expression after acupuncture had repair effects on injured nerve cells, indicating that heroin relapse caused a compensatory increase in brain-derived neurotrophic factor and glial cell line-derived neurotrophic factor expression in the ventral tegmental area, and acupuncture increased brain-derived neurotrophic factor and glial cell line-derived neurotrophic factor expression. This result is helpful to explain why acupuncture can protect nerve cells against injury.
Knowledge of the effects of acupuncture in traditional Chinese medicine
Traditional Chinese medicine believes that Baihui is strongly associated with the brain, and acupuncture at Baihui can regulate cerebral functions. Acupuncture at Baihui induces consciousness-restoring resuscitation, calms the nerves, dredges Du meridian, and relieves epilepsy. Dazhui is the crossing point where the three Yang Meridians of the Hand and the Du meridian cross and converge. New Compilation of Acupuncture Points says that Dazhui is an essential point in the body, and acupuncture at Dazhui can release various nervous symptoms. Acupuncture at Baihui and Dazhui contributes to the recovery of nerve functions, increases brain-derived neurotrophic factor and glial cell line-derived neurotrophic factor expression in the rat frontal lobe and ventral tegmental area. Taken together, acupuncture has a promoting effect on nerve regeneration, repair and plasticity in heroin relapse rats.
Materials and Methods
Design
A randomized controlled animal study.
Time and setting
Experiments were performed at the Institute of Acupuncture and Meridian, Anhui University of Chinese Medicine, China in January 2013.
Materials
Animals
A total of 32 (16 males, 16 females) clean, Wistar rats aged 4 months and weighing 200 ± 20 g were provided by the Experimental Animal Center, Nanjing Medical University, China (license No. SYXK (Su) 2008-0007). All rats were allowed free access to standard solid feed at 22 ± 2°C and maintained in relative humidity of 50–70%. Experimental disposals were performed in accordance with the Guidance Suggestions for the Care and Use of Laboratory Animals, formulated by the Ministry of Science and Technology of China[58].
Drugs
Heroin, a derivative of diacetylmorphine, chemical formula C21H23NO5, purity 90%, was provided and identified by Anhui Provincial Narcotic Prohibition Office in China. Heroin was diluted by physiological saline. Methadone, chemical formula C21H27NO·HCl, preparation for oral use, specification 10 mg/10 mL, was purchased from Central Pharmaceutical Co., Ltd., Tianjin, China, Approval No. GYZZ H10970303, lot No. 090919.
Methods
Establishment of a rat model of heroin relapse
An increasing amount of heroin was injected into the left gastrocnemius muscle of the posterior lower limb for 8 consecutive days (as narcotics use). From day 1 to day 8, 0.8, 1.2, 1.6, 2.0, 2.4, 2.8, 3.2 and 3.6 mg heroin was injected daily. From day 1 to day 6, the injection was performed once a day. From day 7 to day 8, injection was conducted twice a day (1.6 mg once on day 7, and 1.8 mg once on day 8). The rats received heroin at 7:00 and 19:00. After using narcotics, intramuscular injection of heroin was terminated for 5 days. Withdrawal symptoms and conditioned place preference were used to judge whether the model was established. Natural withdrawal was considered as detoxification. The rat model of heroin relapse was established using the method of narcotics use (addiction) → detoxification, and the addiction and detoxification process was repeated three times[59]. The rats in the normal group were administered physiological saline during narcotics use, 0.2 mL/time.
Acupuncture treatment
The rats in the acupuncture group underwent acupuncture during the period of detoxification. The rats were gently placed in a tailor-made fixator. In accordance with _the Acupuncture Atlas in Rats_[60], acupuncture at Baihui (on the head, the midpoint of the anterior hairline, at the midpoint of the line connection the apexes of both ears) and Dazhui (on the posterior median line, in the depression below the spinous process of the 7th cervical vertebra) was conducted using a 25 mm stainless steel acupuncture needle (0.30 mm diameter, 25 mm long; Suzhou Medical Sino-foreign Joint Venture, Suzhou, Jiangsu Province, China) at an angle of 30° and with a depth of 12 mm. The needle was held in place for 30 minutes. Acupuncture was carried out once at 7:00 a.m. every day, for 5 consecutive days.
Intragastric administration of methadone
A decreasing amount of methadone was intragastrically given to the rats in the methadone group during the period of detoxification. From day 1 to day 4, the dose of methadone was respectively 0.4, 0.3, 0.2 and 0.1 mg.
Specimen collection and transmission electron microscopy for neuronal ultrastructure in the ventral tegmental area of rats
All rats were anesthetized with 10% chloral hydrate (0.36 mL/100 g) via intraperitoneal injection. After aortic cannulation, the right atrium was cut, perfused with 0.1 mol/L PBS 250 mL, and fixed with 4% paraformaldehyde + 0.1 mol/L PBS 150 mL for 30 minutes. In accordance with _The Rat Brain in Stereotaxic Coordinates_[61], the rats were decapitated, and the ventral tegmental area of one hemisphere was obtained and cut into 1 mm3 blocks. These blocks were fixed in a 2.5% glutaral for 24 hours, immersed in PBS for 1–6 hours, fixed in 1% osmic acid for 1–2 hours, sliced into 70 nm-thick sections, and observed with a transmission electron microscope (JEM-1230; JEOL, Tokyo, Japan).
Immunohistochemical staining for brain-derived neurotrophic factor and glial cell line-derived neurotrophic factor expression in the ventral tegmental area of rats
The ventral tegmental area of another hemisphere was fixed in 4% paraformaldehyde, dehydrated in alcohol, permeabilized in xylene, embedded in paraffin, and then serially sliced into 4 μm-thick sections. These sections were incubated with rabbit anti-rat brain-derived neurotrophic factor monoclonal antibody (1:100; Beijing Biosynthesis Biotechnology Co., Ltd., Beijing, China) and rabbit anti-rat glial cell line-derived neurotrophic factor monoclonal antibody (1:100; Beijing Biosynthesis Biotechnology Co., Ltd.) in a wet box overnight at 4°C, followed by an incubation in biotinylated goat anti-rabbit IgG (Boster, Wuhan, Hubei Province, China) at room temperature for 20 minutes. Using DP801 morphology image analysis system (Jiangsu JEDA Science-Technology Development Co., Ltd., Nanjing, Jiangsu Province, China), three discontinuous sections of each rat were selected, and five nonoverlapping visual fields of each section were selected under a light microscope (× 20) for cell counting. Cells with brown particles in the cytoplasm were considered as positive cells. The number of positive cells in each visual field, and mean absorbance of each section were calculated.
Statistical analysis
Experimental results were expressed as mean ± SD, and processed with SPSS 13.0 software (SPSS, Chicago, IL, USA). The differences among multiple groups were compared using one-way analysis of variance. Paired comparison was performed using paired _t_-test. A value of P < 0.05 was considered statistically significant.
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Funding: This study was supported by the National Natural Science Foundation of China, No. 81173325; the Anhui Provincial Higher Learning School Excellent Youth Project, No. 2010SQRL105; Anhui Provincial Higher Learning Natural Science Project, No. KJ2013Z180.
Conflicts of interest:None declared.
Peer review:This study observed cell structure and neurotrophic factor changes of the ventral tegmental area of heroin relapse rats. Results verified that acupuncture at Baihui and Dazhui could protect neurons against injury in heroin relapse rats and confirmed the mechanisms of acupuncture effects on detoxification.
Copyedited by Apricò K, Bai WZ, Liang Y, Yu J, Qiu Y, Li CH, Song LP, Zhao M
Keywords:
nerve regeneration; acupuncture and moxibustion; heroin relapse rats; neurotrophic factor; nerve cell ultrastructure; acupuncture; midbrain; Dazhui (DU14); Baihui (DU20); NSFC grant; neural regeneration
© 2014 Neural Regeneration Research | Published by Wolters Kluwer – Medknow