Abstract
Background:
The Alzheimer disease (AD) induces the central and peripheral nervous system disruption by increasing oxidative stress; therefore, it induces disruption of the physical condition as well as occurrence of chronic pain.Objectives:
The present study aimed at investigating the interactive effects of endurance training (ET) on positive and negative slope and royal jelly (RJ) consumption on motor balance and pain threshold in animal model of AD.Methods:
The current experimental study was conducted on 49 male Wister rats with AD divided equally into seven groups including AD control (ADC), ET on positive slope (ETPS), ET on negative slope (ETNS), sham (RJ solvent) (SH), ETPS + RJ, ETNS + RJ, and RJ. In order to investigate the effect of AD induction on motor balance and pain threshold, seven rats were assigned into the healthy control (HC) group. The rats in the ET groups performed ET for four weeks and five 60-minute sessions weekly, and the RJ groups received 100 mg/kg RJ daily for four weeks. One-way ANOVA and two-way ANOVA with Bonferroni post-hoc tests were employed to analyze the data (P ≤ 0.05).Results:
ETPS, ETNS, and RJ consumption significantly increased motor balance in rats with AD (P ≤ 0.05). Also, ET and RJ consumption had interactive effects on increasing the motor balance in rats with AD (P ≤ 0.05). ETPS significantly reduced pain threshold in rats with AD (P ≤ 0.05); nevertheless, ET and RJ consumption had no interactive effects on reduction of the pain threshold in rats with AD (P ≥ 0.05).Conclusions:
It seems that to improve the motor balance in AD, ETPS and ETNS can be employed with RJ consumption.Keywords
1. Background
Today, one of the important medical goals is to improve the quality of life in people with cognitive impairment and motor limitation and reduce unknown pain caused by dementia (1, 2). It is reported that unknown pain causes health problems and reduces quality of life in patients with dementia; studies also show that such pain can reduce desire to perform physical activity by decreasing the range of motion (3). The noted disorders in people with mental impairment induce an impairment called falling syndrome, which affects a significant number of elderly people (1).
Clinically, the Alzheimer disease (AD) and central and peripheral nervous system disorders impair the sensory-motor system and cause pain (3, 4). Since increased inflammation and decreased function of the nervous system are closely related to pain and decreased muscle strength and balance (5), it seems that increased oxidative stress caused by AD in the central and peripheral nervous system reduces neurotrophins (4), range of motion and balance, and increases chronic and unknown pain; therefore, it has significant effects on progression of AD.
Today, physical activity is considered as an undeniable necessity for the health and well-being by researchers. Exercise seems to be associated with increased β-endorphins in the somatic nervous system, decreased function of the sympathetic nervous system (6), and increased coordination of the nerve and muscle for voluntary control of body movements; it also improves the performance of this system and reduces peripheral pain (6, 7). In this regard, researches show that regular exercise increases the static and dynamic balance (8, 9), pain relief, and quality of life (8) in the elderly; it also reduces pain in elderly rats (10). Nevertheless, it was observed that core stability training had no significant effect on balance (11).
According to contradictory results regarding the effect of exercise type on balance and pain, using complementary medicine and natural products due to fewer side effects can improve symptoms of degenerative disorders. Recently, many researchers investigated the biological effects of the royal jelly (RJ) secreted by hypopharyngeal and submandibular glands of young bees (12). Researchers report that RJ by differentiation, proliferation, and repair of neurons has desirable effects on various brain parts associated with movement and balance (13) and induces its analgesic effects by increasing serotonin (14). In this regard, the consumption of 800 mg/kg RJ had pain relief, anti-depressant, and anti-anxiety effects on postmenopausal females (14).
2. Objectives
The mechanism of action and effect of the type of muscle contraction seem to be essential factors in increasing the dynamic and static balance. To the best of authors’ knowledge, no study was conducted so far on the effects of eccentric and concentric endurance training (ET) on balance or RJ consumption on the treatment of some diseases; therefore, authors tried to open a new window of research for sport nutritionists. The present study aimed at investigating the interactive effects of ET on positive slope (ETPS) and negative slope (ETNS) along with RJ consumption on motor balance and pain threshold in animal model of AD.
3. Methods
The current experimental study was conducted on 56 male rats obtained from the Animal Breeding Center of the Islamic Azad University, Marvdasht Branch, Iran. Animals were transferred to the sports physiology lab and maintained under standard conditions for seven days in transparent polycarbonate autoclaving cages with the optimum temperature of 20°C - 24°C, relative humidity of 55% - 65%, 12:12 hour light-dark cycle, and free access to water and standard food pellets including crude protein 23%, crude fat 3.5% - 4.5%, crude fiber 4% - 4.5%, ash maximum 10%, calcium 0.95% - 1%, phosphorus 0.65% - 0.75%, salt 5% - 5.5%, humidity maximum 10%, lysine 1.15%, methionine 0.33%, methionine + cysteine 0.63%, threonine 0.72%, and tryptophan 0.25%. On the 8th day, 49 rats were injected 8 mg/kg trimethyltin chloride (TMT) intra-peritoneally (15) and three days (15) later after confirmation of hippocampus degeneration, AD symptoms were observed by a number of behavioral changes in rats. These clinical symptoms included muscle tremors, elevated body temperature, nausea, seizure, and tail twists. The rats with AD were equally divided into seven groups including AD control (ADC), ETPS, ETNS, sham (RJ solvent) (SH), ETPS + RJ, ETNS + RJ, and RJ. Also, in order to investigate the effects of AD induction on motor balance and pain threshold, seven rats were assigned into the healthy control (HC) group. ETPS (at a speed of 16 m/minute on a positive slope) and ETNS (at a speed of 16 m/minute on a negative slope) groups ran on a treadmill for five 60-minute sessions weekly for four weeks (16). The RJ groups received 100 mg/kg RJ daily for four weeks (17); 48 hours after the last training session and JR administration, the motor balance was measured by a rotarod apparatus and pain threshold was measured by a hot plate device.
3.1. Endurance Training Protocol
In order to perform ET, the rats ran for five minutes at a speed of 8 m/minute on a zero-inclined treadmill; then, ran with +15% and -15% slopes at the speed of 15 cm/second in the 1st week; 5 cm/second was added to the speed of treadmill per week. At the end of each training session, rats were cooled down for five minutes at a speed of 8 m/minute on a zero slope (16).
3.2. Motor Balance Test
The ability of rats to maintain balance and motor coordination was measured using a rotarod (Danesh Salar Iranian Company, Iran). For this purpose, the rats were placed on the device for three minutes for acclimation and were trained based on the original protocol (10 rpm cycling speed with 7 rpm2 velocity) and after 30 minutes, the balance test was performed (10 rpm with 7 rpm2 velocity), which was approximately 10 - 11 rpm. The duration of balance maintenance on the wheel was recorded in seconds for each animal. The total time was 300 seconds. The test was performed for each rat in triplicate with approximately 30 minutes interval, and the average was considered in the analysis (18).
3.3. Pain Threshold Test
To acclimate the animals to the device, the rats were placed on a hot plate device for about three minutes while it was off. On the test day, the rats were placed on a hot plate heated to 52.8°C and the interval between the placement of the rat on the device and the first reaction including lifting the leg, jumping, and trembling the feet simultaneous with lifting was considered as the pain threshold at the time that was measured by a chronometer; besides, to prevent tissue damage, the test lasted less than 60 seconds for each rat (19).
3.4. Statistical Analysis
To analyze the data, the Shapiro-Wilk, one-way ANOVA, two-way ANOVA, and Bonferroni post-hoc tests were used (P ≤ 0.05).
4. Results
Mean and standard deviation of motor balance and pain threshold in the rats are shown in Figures 1 and 2. The results of one-way ANOVA showed a significant difference in motor balance among HC, ADC, and SH groups (P = 0.001). The results of Bonferroni post-hoc test showed that AD induction had a significant impact on the reduction of motor balance (P = 0.003); however, there was no significant difference in motor balance between SH and ADC groups (P = 0.94) (Figure 1). The results of one-way ANOVA showed a significant difference in pain threshold among HC, ADC, and SH groups (P = 0.002). The results of Bonferroni post-hoc test showed that AD induction had a significant impact on the reduction of pain threshold (P = 0.01); however, there was no significant difference in pain threshold between SH and ADC groups (P = 0.75) (Figure 2). The results of two-way ANOVA showed that training (P = 0.002) and RJ consumption (P = 0.005) significantly improved the motor balance in rats with AD; also, training and RJ consumption had an interactive effect on the improvement of motor balance in rats with AD (P = 0.001). The results of Bonferroni post-hoc test showed that ETPS (P = 0.001) and ETNS (P = 0.001) significantly improved motor balance and no significant difference was observed between the results (P = 0.59) (Figure 1). The results of two-way ANOVA showed that training (P = 0.01) significantly increased pain threshold in rats with AD; nevertheless, RJ consumption (P = 0.61) had no significant effect on pain threshold; also, training and RJ consumption had no interactive effects on pain threshold in rats with AD (P = 0.65). The results of Bonferroni post-hoc test showed that ETPS (P = 0.01) significantly increased pain threshold; while ETNS had no significant effects on this variable (P = 0.99) (Figure 2).
Motor balance in the study groups; data are expressed as mean ± SEM. **, P < 0.01 comparison of ADC and HC groups; +++, P < 0.001 a significant effect on the improvement of motor balance; $$$, P < 0.001 an interactive effect on the improvement of motor balance (HC, healthy control; ADC, the Alzheimer disease control; SH, sham; ETPS, endurance training on positive slope; ETNS, endurance training on negative slope; RJ, royal jelly).
Pain threshold in the study groups; data are expressed as mean ± SEM. **, P <0.01 comparison of ADC and the HC groups; ++, P < 0.01 a significant effect on the increase of pain threshold (HC, healthy control; ADC, the Alzheimer disease control; SH, sham; ETPS, endurance training on positive slope; ETNS, endurance training on negative slope; RJ, royal jelly).
5. Discussion
Results of the present study showed that induction of AD by TMT significantly reduced the motor balance and pain threshold in rats. However, four weeks of ETPS and ETNS significantly improved motor balance, and ETPS significantly increased pain threshold in rats with AD. TMT is an organotin compound that causes selective destruction in the central nervous system. It is a neurotoxin, which induces neuronal death in the entire central and peripheral nervous system (15). The increased oxidative stress produced by TMT in the cells induces damage to nociceptors (20) and causes behavioral disorders, loss of balance, and muscle seizure in various areas of the body (15). It is reported that the administration of 8 mg/kg of TMT significantly reduces the density of the granular cells in the rat follicles (21), increases the level of reactive oxygen species (22), and elevates pain in the central and peripheral nervous system (23). On the other hand, the present study showed that ETPS significantly improved motor balance and increased pain threshold in rats with AD. Authors believe that physiological adaptations to exercises can improve the utilization of motor units and increase the vitality of the motor cortex in elderly people (24) through the reduction of oxidative stress and sympathetic system activity (25) as well as the increase of neurotrophins (26). In line with the present study findings, physical activity had a significant effect on the improvement of static and dynamic balance in the elderly (24); exercise training had a significant effect on improving motor balance and quality of life (27), and modified exercises had significant pain relief effects (28); nevertheless, weight-bearing training did not have a significant effect on dynamic balance in elderly males (29). The contradictory results can be explained by differences in the statistical population, type, intensity, and duration of exercises.
The results of the present study showed that RJ consumption significantly improved motor balance in rats with AD; however, it had no significant effect on pain threshold. It is reported that RJ consumption, in addition to antioxidant effects, could mimic the activity of brain-derived neurotrophic factor and directly help the regeneration of neural cells and neurogenesis (13). RJ helps to improve balance maintenance through a regulatory mechanism of increasing the steroid receptors and serotonin (as a major factor in pain management) (13) and also the increase in the expression of proteins involved in hypertrophy (30). Although studies are limited to the effect of RJ consumption on motor balance maintenance, researchers showed that the dose-dependent RJ consumption had a significant effect on the improvement of balance in mice (30); also, consumption of 800 mg RJ for 12 weeks had significant pain relief and anti-depressant effects in postmenopausal females (13). The incompatibility of the noted findings with those of the present study could be attributed to differences in the statistical population and dose of RJ; therefore, it seems that further studies in this area can be hopeful to improve motor balance and reduce pain.
Both ETPS and ETNS with RJ consumption had interactive effects on motor balance in rats with AD; nevertheless, they had no interactive effects on pain threshold. According to the reported studies, common mechanisms of action of exercises and RJ consumption in improving motor balance and pain threshold could increase antioxidant factors (13, 25) and neurotrophins (13, 26). Also, the dose of RJ seems to play an important role in exerting its analgesic effects. Therefore, it is suggested that different doses of RJ be examined in future studies. Considering the physiological effects of exercise and RJ consumption, it seems that the lack of evaluation of physiological changes in the central and peripheral nervous system related to motor balance and pain such as muscle mass, strength, and serotonin and prostaglandin levels were the limitations of the current study. Therefore, it is recommended measuring these physiological indicators along with motor balance and pain threshold in future studies.
5.1. Conclusions
It seems that ET on positive and negative slope and RJ consumption separately and in combination have desirable effects on motor balance improvement in rats with AD; however, analgesic effects were just observed in ET on positive slope.
Acknowledgements
References
-
1.
Montero-Odasso M, Pieruccini-Faria F, Bartha R, Black SE, Finger E, Freedman M, et al. Motor phenotype in neurodegenerative disorders: Gait and balance platform study design protocol for the ontario neurodegenerative research initiative (ONDRI). J Alzheimers Dis. 2017;59(2):707-21. [PubMed ID: 28671116]. [PubMed Central ID: PMC5523841]. https://doi.org/10.3233/JAD-170149.
-
2.
Husebo BS, Achterberg W, Flo E. Identifying and managing pain in people with Alzheimer's disease and other types of dementia: A systematic review. CNS Drugs. 2016;30(6):481-97. [PubMed ID: 27240869]. [PubMed Central ID: PMC4920848]. https://doi.org/10.1007/s40263-016-0342-7.
-
3.
Buchman AS, Bennett DA. Loss of motor function in preclinical Alzheimer's disease. Expert Rev Neurother. 2011;11(5):665-76. [PubMed ID: 21539487]. [PubMed Central ID: PMC3121966]. https://doi.org/10.1586/ern.11.57.
-
4.
Monroe TB, Gore JC, Chen LM, Mion LC, Cowan RL. Pain in people with Alzheimer disease: Potential applications for psychophysical and neurophysiological research. J Geriatr Psychiatry Neurol. 2012;25(4):240-55. [PubMed ID: 23277361]. [PubMed Central ID: PMC4455539]. https://doi.org/10.1177/0891988712466457.
-
5.
Bello AI, Ababio E, Antwi-Baffoe S, Seidu MA, Adjei DN. Pain, range of motion and activity level as correlates of dynamic balance among elderly people with musculoskeletal disorder. Ghana Med J. 2014;48(4):214-8. [PubMed ID: 25709137]. [PubMed Central ID: PMC4335435]. https://doi.org/10.4314/gmj.v48i4.8.
-
6.
Reis AD, Pereira P, Diniz RR, de Castro Filha JGL, Dos Santos AM, Ramallo BT, et al. Effect of exercise on pain and functional capacity in breast cancer patients. Health Qual Life Outcomes. 2018;16(1):58. [PubMed ID: 29625622]. [PubMed Central ID: PMC5889570]. https://doi.org/10.1186/s12955-018-0882-2.
-
7.
Alivand F, Karimzadeh F. The effect of exercise on the memory improvement: A review of cellular and molecular mechanisms. Neurosci J Shefaye Khatam. 2015;3(4):123-30. https://doi.org/10.18869/acadpub.shefa.3.4.123.
-
8.
Toulotte C, Thevenon A, Fabre C. [Effects of training on static and dynamic balance in elderly subjects who have had a fall or not]. Ann Readapt Med Phys. 2004;47(9):604-10. French. [PubMed ID: 15539067]. https://doi.org/10.1016/j.annrmp.2004.03.004.
-
9.
Avelar BP, Costa JN, Safons MP, Dutra MT, Bottaro M, Gobbi S, et al. Balance exercises circuit improves muscle strength, balance, and functional performance in older women. Age (Dordr). 2016;38(1):14. [PubMed ID: 26802006]. [PubMed Central ID: PMC5005874]. https://doi.org/10.1007/s11357-016-9872-7.
-
10.
Hirase T, Kataoka H, Inokuchi S, Nakano J, Sakamoto J, Okita M. Effects of exercise training combined with increased physical activity to prevent chronic pain in community-dwelling older adults: A preliminary randomized controlled trial. Pain Res Manag. 2018;2018:2132039. [PubMed ID: 29849840]. [PubMed Central ID: PMC5907421]. https://doi.org/10.1155/2018/2132039.
-
11.
DeBolt LS, McCubbin JA. The effects of home-based resistance exercise on balance, power, and mobility in adults with multiple sclerosis. Arch Phys Med Rehabil. 2004;85(2):290-7. [PubMed ID: 14966716]. https://doi.org/10.1016/j.apmr.2003.06.003.
-
12.
Hashimoto M, Kanda M, Ikeno K, Hayashi Y, Nakamura T, Ogawa Y, et al. Oral administration of royal jelly facilitates mRNA expression of glial cell line-derived neurotrophic factor and neurofilament H in the hippocampus of the adult mouse brain. Biosci Biotechnol Biochem. 2005;69(4):800-5. [PubMed ID: 15849420]. https://doi.org/10.1271/bbb.69.800.
-
13.
Zamani Z, Reisi P, Alaei H, Pilehvarian AA. Effect of royal jelly on improving passive avoidance learning and spatial learning and memory in rats. SSU J. 2012;20(2):211-9.
-
14.
Asama T, Matsuzaki H, Fukushima S, Tatefuji T, Hashimoto K, Takeda T. Royal jelly supplementation improves menopausal symptoms such as backache, low back pain, and anxiety in postmenopausal japanese women. Evid Based Complement Alternat Med. 2018;2018:4868412. [PubMed ID: 29853955]. [PubMed Central ID: PMC5949161]. https://doi.org/10.1155/2018/4868412.
-
15.
Malekzadeh S, Edalatmanesh MA, Mehrabani D, Shariati M, Malekzadeh S. Drugs induced Alzheimer's disease in animal model. Galen Med J. 2017;6(3):96-185.
-
16.
Kang YS, Kim CH, Kim JS. The effects of downhill and uphill exercise training on osteogenesis-related factors in ovariectomy-induced bone loss. J Exerc Nutrition Biochem. 2017;21(3):1-10. [PubMed ID: 29036760]. [PubMed Central ID: PMC5643207]. https://doi.org/10.20463/jenb.2017.0010.
-
17.
Arzi A, Houshmand G, Goudarzi M, Khadem Haghighian H, Rashidi Nooshabadi MR. Comparison of the analgesic effects of royal jelly with morphine and aspirin in rats using the formalin. J Babol Univ Med Sci. 2015;17(2):50-6.
-
18.
Mallet PE, Beninger RJ, Flesher SN, Jhamandas K, Boegman RJ. Nucleus basalis lesions: implication of basoamygdaloid cholinergic pathways in memory. Brain Res Bull. 1995;36(1):51-6. [PubMed ID: 7882049]. https://doi.org/10.1016/0361-9230(94)00162-t.
-
19.
Luesse HG, Schiefer J, Spruenken A, Puls C, Block F, Kosinski CM. Evaluation of R6/2 HD transgenic mice for therapeutic studies in Huntington's disease: Behavioral testing and impact of diabetes mellitus. Behav Brain Res. 2001;126(1-2):185-95. [PubMed ID: 11704263]. https://doi.org/10.1016/s0166-4328(01)00261-3.
-
20.
Farbood Y, Sarkaki A, Hashemi S, Mansouri MT, Dianat M. The effects of gallic acid on pain and memory following transient global ischemia/reperfusion in Wistar rats. Avicenna J Phytomed. 2013;3(4):329-40. [PubMed ID: 25050290]. [PubMed Central ID: PMC4075730].
-
21.
Shams-Alam S, Edalatmanesh MA. The effete of lithium chloride on the granular cell density in cerebellar folia V and VI in a trimethyltin intoxication model. Neurosci J Shefaye Khatam. 2015;3(2):41-8. https://doi.org/10.18869/acadpub.shefa.3.2.41.
-
22.
Wang X, Cai J, Zhang J, Wang C, Yu A, Chen Y, et al. Acute trimethyltin exposure induces oxidative stress response and neuronal apoptosis in Sebastiscus marmoratus. Aquat Toxicol. 2008;90(1):58-64. [PubMed ID: 18801585]. https://doi.org/10.1016/j.aquatox.2008.07.017.
-
23.
Carrasco C, Naziroglu M, Rodriguez AB, Pariente JA. Neuropathic pain: Delving into the oxidative origin and the possible implication of transient receptor potential channels. Front Physiol. 2018;9:95. [PubMed ID: 29491840]. [PubMed Central ID: PMC5817076]. https://doi.org/10.3389/fphys.2018.00095.
-
24.
Ghasempour L, Hoseini FS, Soleymani M, Ahmadi M. Effects of physical fitness exercise, mental exercise and mindfulness exercise on static and dynamic balance in elderly women. Salmand. 2017;12(2):197-211. https://doi.org/10.21859/sija-1202180.
-
25.
Polli A, Van Oosterwijck J, Nijs J, Marusic U, De Wandele I, Paul L, et al. Relationship between exercise-induced oxidative stress changes and parasympathetic activity in chronic fatigue syndrome: An observational study in patients and healthy subjects. Clin Ther. 2019;41(4):641-55. [PubMed ID: 30665828]. https://doi.org/10.1016/j.clinthera.2018.12.012.
-
26.
Roh HT, So WY. The effects of aerobic exercise training on oxidant-antioxidant balance, neurotrophic factor levels, and blood-brain barrier function in obese and non-obese men. J Sport Health Sci. 2017;6(4):447-53. [PubMed ID: 30356625]. [PubMed Central ID: PMC6189263]. https://doi.org/10.1016/j.jshs.2016.07.006.
-
27.
Holthoff VA, Marschner K, Scharf M, Steding J, Meyer S, Koch R, et al. Effects of physical activity training in patients with Alzheimer's dementia: Results of a pilot RCT study. PLoS One. 2015;10(4). e0121478. [PubMed ID: 25884637]. [PubMed Central ID: PMC4401690]. https://doi.org/10.1371/journal.pone.0121478.
-
28.
Akkan H, Gelecek N. The effect of stabilization exercise training on pain and functional status in patients with cervical radiculopathy. J Back Musculoskelet Rehabil. 2018;31(2):247-52. [PubMed ID: 28946516]. https://doi.org/10.3233/BMR-169583.
-
29.
Tsaklis PV, Grooten WJ, Franzen E. Effects of weight-shift training on balance control and weight distribution in chronic stroke: A pilot study. Top Stroke Rehabil. 2012;19(1):23-31. [PubMed ID: 22306625]. https://doi.org/10.1310/tsr1901-23.
-
30.
Okumura N, Toda T, Ozawa Y, Watanabe K, Ikuta T, Tatefuji T, et al. Royal jelly delays motor functional impairment during aging in genetically heterogeneous male mice. Nutrients. 2018;10(9). [PubMed ID: 30200401]. [PubMed Central ID: PMC6164577]. https://doi.org/10.3390/nu10091191.