Skip to main content
Interdisciplinary Toxicology logoLink to Interdisciplinary Toxicology
. 2019 Oct 18;11(3):217–220. doi: 10.2478/intox-2018-0020

Beneficial effect of 6 weeks lasting handling of adult rats on spatial memory in experimental model of neurodegeneration

Veronika Stara 1,2,, Mojmir Mach 1, Eduard Ujhazy 1, Boris Liptak 1,3, Zdenka Gasparova 1
PMCID: PMC6853005  PMID: 31736636

Abstract

Handling is a form of experience which can result in physiological changes depending on the period of postnatal age when performed. There is a lot of evidence about the positive effect of neonatal handling, but a lack dealing with handling of adult rats. Behavioral changes and memory deficits are present in dementia-like disorders. In the present work, we tested whether 6 weeks lasting handling of young adult rats could revert memory impairment induced by trimethyltin (TMT) (7.5 mg/kg, intraperitoneally). Testing rats in Morris water maze revealed significant effect of TMT as well significant effect of handling. We observed improvement of spatial memory also between healthy, non-degenerated rats as well as degenerated rats, represented by shorter latency onto the platform. In our paper, we report beneficial effect of handling on spatial memory that is in compliance with published works about beneficial effect of cognitive therapy and training in patients with early stage of Alzheimer΄s disease and dementia.

Keywords: trimethyltin, handling, memory, neurodegeneration

Introduction

Life experiences and environmental factors can modulate animal physiology, behavior and memory (Del Arco et al., 2007; Levine, 2001; Winterfeld, 1998). In 2003 Frick and Fernandez demonstrated beneficial effect of enrichment on spatial memory in adult female mice. Another intervention, handling, was broadly investigated in neonates. In adult and old rats, early postnatal handling has been shown to reduce anxiety, decrease levels of prolactin and corticosterone following stress, prevent age-related loss of hippocampal CA1 and CA3 pyramidal cells and deterioration of working memory and recognition memory (Boufleur et al., 2013; Fenoglio et al., 2005; Ferré et al., 1995; Meaney et al., 1988; Meerlo et al., 1999; Stamatakis et al., 2008; Valée et al., 1999; Viau et al., 1993). The above mentioned neonatal handling mediated memory improvement was accompanied by increase in dendritic length and dendritic spine density in the cortex (Richards et al., 2012). Positive effect of early postnatal handling has been shown on prenatal stress, alcohol exposure and malnutrition in experimental rats (Raineki et al., 2014). Much less is known about the consequence of handling of adult rats (Costa et al., 2012; Deutsch-Feldman et al., 2015).

In our study, we focused on the effect of late postnatal handling on spatial memory in experimental model of dementia induced by trimethyltin (TMT). TMT has a harming effect on the hippocampus that together with memory damage makes TMT a useful tool for studying perspective neuroprotective drugs (Geloso et al., 2011). With the perspectivity of stannin, a key protein involved in TMT sensitivity, TMT is responsible for disruption of calcium homeostasis, production of reactive oxygen species, increment in levels of malondialdehyde, astrocyte activation and reactive gliosis, as well as the spread of neuronal apoptosis leading to functional deterioration of synaptic transmission (Corvino et al., 2011; Gasparova et al., 2012; Kaur et al., 2013; Piacentini et al., 2008; Thompson et al., 1996). It is learning and cognition decline that is a typical hallmark of dementia (Gutiérrez-Rexach & Schatz, 2016; Popa-Wagner et al., 2015). In patients with cognitive impairment tactile stimulation and cognitive exercise improved memory (Gates et al., 2011; Scherder et al., 1995).

Our hypothesis to test the effect of handling on neurodegeneration-induced rats was based on our previous observation when 28 days lasting oral administration of aqua pro injectione (vehiculum) to rats showed better achievement in Morris water maze test compared to our control groups of rats in experiments without such regular manipulation with animals. We wanted to verify whether handling could be beneficial not only for unaffected control rats but even for neurodegeneration induced rats. We decided to test rat spatial memory in Morris water maze, a behavioral test best suitable for testing spatial memory and learning (Vorhees & Williams, 2006) on the model of TMT-induced neurodegeneration with aspect of handling. In the current study we report beneficial effect of late handling on learning and spatial memory in intact and degenerated adult rats.

Materials and methods

Animals

Male Wistar rats (n=32), 8 weeks old, weighing 197±1.3 g at the beginning of the 8-week lasting experiment came from the breeding station Dobra Voda of the Institute of Experimental Pharmacology and Toxicology (Slovak Republic, reg. No. SK CH 24011). All procedures with animals were performed in compliance with the principles of laboratory animal care issued by EU Directive 2010/63/EU for animal experiments, proved and controlled by the State Veterinary and Food Administration of Slovakia and the Ethical Committee of the Institute of Experimental Pharmacology and Toxicology, Slovak Academy of Sciences. The rats were housed in plastic cages (4 rats per cage) with pelletful food (KKZ-P/M) and water ad libitum.

Experimental procedure

After 7-day adaptation, the rats were randomly allocated into 4 groups (n=8/group):

  • Control handled group (C-H),

  • Control non-handled group (C-NH),

  • TMT handled group (TMT-H),

  • TMT non-handled group (TMT-NH).

Control rats received a single i.p. dose of saline (with 0.1% DMSO). TMT rats were affected by a single i.p. dose of TMT chloride (7.5 mg/kg; dissolved in 0.1% DMSO; Sigma-Aldrich, USA) in the volume of 0.2 ml/100 g of rat weight. Four weeks prior to the TMT or vehicle administration, handling was performed on the C-H and TMT-H groups. Altogether handling lasted for 6 weeks (7 days per week), including 2 weeks after TMT/vehicle administration, and ended one week before the Morris water maze test. Handling consisted of tactile stimulation of rats, 10 minutes per cage/day. The rats were also allowed to enter the nearest table next to their cage during handling. Non-handled groups of rats were left undisturbed in the next room.

Morris water maze

The testing in Morris water maze was performed with the hidden platform positioned on the same place during five subsequent days without probe trial on last day according to Gasparova et al. (2014). Briefly, the rats were tested in the range of the 21st till the 25th day (beginning at 7 a.m.) after TMT/or saline administration. The platform was hidden 0.5 cm under the water (23 °C) surface of the pool with a diameter of 180 cm. Each rat was placed in succesive steps into each of the 4 quadrants of the pool every day. The rat had 60 seconds to find the platform. After finding the platform, the animal was left on the platform for 20 seconds. After completion of the 4th quadrant, each animal was carefully dried and placed under a lamp. The data were collected by a camera located above the pool and connected to the computer with the ANY-maze videotracking software (Stoelting Europe, Ireland).

Statistics

Values are means ± SEM. Data obtained from Morris water maze were analyzed using Statistica 7.0 software, Fisher´s least significant difference test. Body mass gain was analyzed using two factorial ANOVA for independent samples.

Results

Six weeks lasting handling resulted in significant reduction of body weight gain in both handled groups compared to respective non-handled groups. Body weight gain of handled TMT-treated group did not differ from handled saline-treated group (Figure 1). The observed body weight gain reduction was the effect of handling in the mentioned corresponding groups (F(1,28)=20.93; p<0.001).

Figure 1.

Figure 1

Effect of 6 weeks handling and treatment on body weight gain. Data are expressed as mean ± SEM, *p<0.05 compared to non-handled group.

Percentual expression of body weight gain of individual groups calculated as a difference between the body weight on the 1st day of handling and after 6 weeks of handling, at the end of the experiment. C-NH group, C-H group, TMT-NH group, TMT-H group. Data are expressed as mean ± SEM, *p<0.05.

In the Morris water maze test, data revealed significant positive effect of handling (F(1,28)=10.05; p<0.01) (Figure 2A) and negative effect of treatment with TMT (F(1,28)=15.23; p<0.001) (Figure 2B) on escape latency to the platform.

Figure 2.

Figure 2

Effect of handling and treatment on latency to find platform in Morris water maze. Data are expressed as mean ± SEM, **p<0.01; ***p<0.001 compared to control.

The effect of handling is expressed as cumulative mean value of escape latency to the platform from both non-handled (NH) vs. handled (H) groups (A) and the effect of treatment is expressed as cumulative mean value from both non-treated (C) vs. both TMT-treated groups (TMT) (B). Data are expressed as mean ± SEM, **p<0.01, ***p<0.001.

The trend of improved spatial memory of handled groups is shown in Figure 3A. Note that the escape latency for TMT-H group is similar to the C-NH group. Total mean escape latency during 5 consecutive days revealed significant amelioration of spatial memory between C-NH and C-H and TMT-NH and TMT-H (Figure 3B).

Figure 3.

Figure 3

Escape latency to the platform. (A) Escape latency to the platform for individual days of testing and mean latency (B) calculated from 5 consecutive days for the given group. Data are expressed as mean ± SEM, *p<0.05, **p<0.01.

Discussion

Diagnostical guidelines characterize Alzheimer dementia (AD) as a continuum dividing it to preclinical stage without symptoms, mild cognitive impairment (MCI) and finally AD (Albert et al., 2011). Garrett and Valle (2014) doubt about this division because of the difficulty in diagnosis, non-uniformity and the confession that memory is malleable, as shown by cognitive training programs in humans (Garrett & Valle, 2014; Kurz et al., 2009). We rate TMT-induced neurodegeneration as a mild cognitive impairment with no neurofibrillary tangles and senile plaques.

In the rat, we show a modulatory effect of long-lasting postnatal handling on spatial memory and learning. Beyond the positive effect of handling on neurodegeneration-induced rats, we also report improvement of spatial memory in control, healthy rats compared to control non-handled group. Costa et al. (2012) showed anxiety reducing effect of handling with improved memory tested in elevated plus-maze test.

Beneficial effect of cognitive training was already observed in patients with MCI and AD (Belleville et al., 2006) and here we demonstrate the beneficial effect of postnatal handling on memory of adult animals with induced neurodegeneration. Along the effect on memory, we also observed significant decrease in body weight of handled rats. On the contrary, Panagiotaropoulos et al. (2004) and Vallée et al. (1996) observed neonatal handling mediated increase in body weight of rats as well as increased food intake in adulthood. Another study using young adult rats revealed no effect of handling of young rats on body weight (Deutsch-Feldman et al., 2015). The reason of discrepancies may origin from the period of development when handling was performed, as well as the duration of handling, that was in our experiment much longer than in the studies mentioned.

In conclusion, we report ameliorated spatial memory in healthy non-treated rats and rats with TMT-induced neurodegeneration when handled for 6 weeks. Because of lack of studies about the effect of handling in adulthood, the explanation of the precise mechanism is still shrouded in mystery. There is a suggestion that the effect of the procedure used in the present experiment and positive effect of cognitive training and tactile stimulation in patients with MCI and AD-like dementia can be based on similar mechanisms. Further investigation is necessary for complete description of this phenomenon.

REFERENCES

  1. Albert MS, DeKosky ST, Dickson D, Dubois B, Feldman HH, Fox NC, Gamst A, Holtzman DM, Jagust WJ, Petersen RC, Snyder PJ, Carrillo MC, Thies B, Phelps CH. The diagnosis of mild cognitive impairment due to Alzheimer’ s disease: recommendations from the National Institute on Aging- Alzheimer’ s Association workgroups on diagnostic guidelines for Alzheimer’ s disease. Alzheimers Dement. 2011;7:270–279. doi: 10.1016/j.jalz.2011.03.008. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Belleville S, Gilbert B, Fontaine F, Gagnon L, Ménard E, Gauthier S. Improvement of episodic memory in persons with mild cognitive impairment and healthy older adults: evidence from a cognitive intervention program. Dement Geriatr Cogn Disord. 2006;22:486–499. doi: 10.1159/000096316. [DOI] [PubMed] [Google Scholar]
  3. Boufleur N, Antoniazzi CT, Pase CS, Benvegnú DM, Dias VT, Segat HJ, Roversi K, Rovesi K, Nora MD, Koakoskia G, Rosa JG, Barcellos LJ, Bürger ME. Neonatal handling prevents anxiety-like symptoms in rats exposed to chronic mild stress: behavioral and oxidative parameters. Stress. 2013;16:321–330. doi: 10.3109/10253890.2012.723075. [DOI] [PubMed] [Google Scholar]
  4. Corvino V, Marchese E, Zarkovic N, Zarkovic K, Cindric M, Waeg G, Michetti F, Geloso MC. Distribution and time-course of 4-hydroxynonenal, heat shock protein 110/105 family members and cyclooxygenase-2 expression in the hippocampus of rat during trimethyltin-induced neurodegeneration. Neurochem Res. 2011;36:1490–1500. doi: 10.1007/s11064-011-0478-2. [DOI] [PubMed] [Google Scholar]
  5. Costa R, Tamascia ML, Nogueira MD, Casarini DE, Marcondes FK. Handling of adolescent rats improves learning and memory and decreases anxiety. J Am Assoc Lab Anim Sci. 2012;51:548–553. [PMC free article] [PubMed] [Google Scholar]
  6. Del Arco A, Segovia G, Garrido P, de Blas M, Mora F. Stress, prefrontal cortex and environmental encrichment: studies on dopamine and acetylcholine release and working memory performance in rats. Behav Brain Res. 2007;176:267–273. doi: 10.1016/j.bbr.2006.10.006. [DOI] [PubMed] [Google Scholar]
  7. Deutsch-Feldman M, Picetti R, Seip-Cammack K, Zhou Y, Kreek MJ. Effects of handling and vehicle injections on adrenocorticotropic and corticosterone concentrations in Sprague-Dawley compared with Lewis rats. J Am Assoc Lab Sci. 2015;54:35–39. [PMC free article] [PubMed] [Google Scholar]
  8. Fenoglio KA, Brunson KL, Avishai-Eliner S, Stone BA, Kapadia BJ, Baram TZ. Enduring, handling-evoked enhancement of hippocampal memory function and glucocorticoid receptor expression involves activation of the corticotropin-releasing factor type 1 receptor. Endocrinology. 2005;146:4090–4096. doi: 10.1210/en.2004-1285. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Ferré P, Núñez JF, García E, Tobeña A, Escorihuela RM, Fernández-Teruel A. Postnatal handling reduces anxiety as measured by emotionality rating and hyponeophagia test sin female rats. Pharmacol Biochem Behav. 1995;51:199–203. doi: 10.1016/0091-3057(94)00419-j. [DOI] [PubMed] [Google Scholar]
  10. Frick KM, Fernandez SM. Enrichment enhances spatial memory and increases synaptophysin levels in aged female mice. Neurobiol Aging. 2003;24:615–626. doi: 10.1016/s0197-4580(02)00138-0. [DOI] [PubMed] [Google Scholar]
  11. Garrett MD, Valle R. A methodological critique of the National Institute of Aging and Alzheimer´s Association Guidelines for Alzheimer´s disease, dementia, and mild cognitive impairments. Dementia. 2016;15:239–254. doi: 10.1177/1471301214525166. [DOI] [PubMed] [Google Scholar]
  12. Gasparova Z, Janega P, Stara V, Ujhazy E. Early and late stage of neurodegeneration induced by trimethyltin in hippocampus and cortex of male Wistar rats. Neuro Endocrinol Lett. 2012;33:689–696. [PubMed] [Google Scholar]
  13. Gasparova Z, Stara V, Janega P, Navarova J, Sedlackova N, Mach M, Ujhazy E. Pyridoindole antioxidant-induced preservation of rat hippocampal pyramidal cell nubmer linked with reduction of oxidative stress yet without influence on cognitive deterioration in Alzheimer-like neurodegeneration. Neuro Endocrinol Lett. 2014;35:454–462. [PubMed] [Google Scholar]
  14. Gates NJ, Sachdev PS, Fiatarone Singh MA, Valenzuela M. Cognitive and memory training in adults at risk of dementia: a systematic review. BMC Geriatr. 2011;11:55. doi: 10.1186/1471-2318-11-55. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Geloso MC, Corvino V, Michetti F. Trimethyltin-induced hippocampal degeneration as a tool to investigate neurodegenerative process. Neurochem Int. 2011;58:729–739. doi: 10.1016/j.neuint.2011.03.009. [DOI] [PubMed] [Google Scholar]
  16. Gutiérrez-Rexach J, Schatz S. Cognitive impairment and pragmatics. Springerplus. 2016;5:127. doi: 10.1186/s40064-016-1759-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Kaur S, Chhabra R, Nehru B. Ginkgo biloba extract attenuates hippocampal neuronal loss and cognitive dysfunction resulting from trimethyltin in mice. Phytomedicine. 2013;20:178–86. doi: 10.1016/j.phymed.2012.10.003. [DOI] [PubMed] [Google Scholar]
  18. Kurz A, Pohl C, Ramsenthaler M, Sorg C. Cognitive rehabilitation in patients with mild cognitive impairment. Int J Geriatr Psychiatry. 2009;24:163–168. doi: 10.1002/gps.2086. [DOI] [PubMed] [Google Scholar]
  19. Levine S. Primary social relationships influence the development of the hypothalamic-pituitary-adrenal axis in the rat. Physiol Behav. 2001;73:255–60. doi: 10.1016/s0031-9384(01)00496-6. [DOI] [PubMed] [Google Scholar]
  20. Meaney MJ, Aitken DH, van Berkel C, Bhatnagar S, Sapolsky RM. Effect of neonatal handling on age-related impairments associated with the hippocampus. Science. 1988;239:766–768. doi: 10.1126/science.3340858. [DOI] [PubMed] [Google Scholar]
  21. Meerlo P, Horvath KM, Nagy GM, Bohus B, Koolhaas JM. The influence of postnatal handling on adult neuroendocrine and behavioural stress reactivity. J Neuroendocrinol. 1999;11:925–933. doi: 10.1046/j.1365-2826.1999.00409.x. [DOI] [PubMed] [Google Scholar]
  22. Panagiotaropoulos T, Papaioannou A, Pondiki S, Prokopiou A, Stylianopoulou F, Gerozissis K. Effect of neonatal handling and sex on basal and chronic stress-induced corticosterone and leptin secretion. Neuroendocrinology. 2004;79:109–118. doi: 10.1159/000076633. [DOI] [PubMed] [Google Scholar]
  23. Piacentini R, Gangitano C, Ceccariglia S, Del Fà A, Azzena GB, Michetti F, Grassi C. Dysregulation of intracellular calcium homeostasis is responsible for neuronal death in an experimental model of selective hippocampal degeneration induced by trimethyltin. J Neurochem. 2008;105:2109–2121. doi: 10.1111/j.1471-4159.2008.05297.x. [DOI] [PubMed] [Google Scholar]
  24. Popa-Wagner A, Buga AM, Popescu B, Muresanu D. Vascular cognitive impairment, dementia, aging and energy demand. A vivious cycle. J Neural Transm. 2015;122:S47–54. doi: 10.1007/s00702-013-1129-3. [DOI] [PubMed] [Google Scholar]
  25. Raineki C, Lucion AB, Weinberg J. Neonatal handling: an overview of the possitive and negative effects. Dev Psychobiol. 2014;56:1613–1625. doi: 10.1002/dev.21241. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Richards S, Mychasiuk R, Kolb B, Gibb R. Tactile stimulation during development alters behaviour and neuroanatomical organization of normal rats. Behav Brain Res. 2012;231:86–91. doi: 10.1016/j.bbr.2012.02.043. [DOI] [PubMed] [Google Scholar]
  27. Scherder E, Bouma A, Steen L. The effects of peripheral tactile stimulation on memory in patients with probable Alzheimer´s disease. Am J Alzheimer Dis. 1995;10:15–21. [Google Scholar]
  28. Stamatakis A, Pondiki S, Kitraki E, Diamantopoulou A, Panagiotaropoulos T, Raftogianni A, Stylianopoulou F. Effetc of neonatal handling on adult spatial learning and memory following acute stress. Stress. 2008;11:148–159. doi: 10.1080/10253890701653039. [DOI] [PubMed] [Google Scholar]
  29. Thompson TA, Lewis JM, Dejneka NS, Severs WB, Polavarapu R, Billingsley ML. Induction of apoptosis by organotin compounds in vitro: neuronal protection with antisense oligonucleotides directed against stannin. J Pharmacol Exp Ther. 1996;276:1201–1216. [PubMed] [Google Scholar]
  30. Vallée M, Mayo W, Maccari S, Le Moal M, Simon H. Long-term effects of prenatal stress and handling on metabolic parameters: relationship to corticosterone secretion response. Brain Res. 1996;712:287–292. doi: 10.1016/0006-8993(95)01459-4. [DOI] [PubMed] [Google Scholar]
  31. Vallée M, MacCari S, Dellu F, Simon H, Le Moal M, Mayo W. Long-term effects of prenatal stress and postnatal handling on age-related glucocorticoid secretion and cognitive performance: a longitudinal study in the rat. Eur J Neurosci. 1999;11:2906–2916. doi: 10.1046/j.1460-9568.1999.00705.x. [DOI] [PubMed] [Google Scholar]
  32. Viau V, Sharma S, Plotsky PM, Meaney MJ. Increased plasma ACTH responses to stress in nonhandled compared with handled rats require basal levels of corticosterone and are associated with increased levels of ACTH secretagogues in the median eminence. J Neurosci. 1993;13:1097–1105. doi: 10.1523/JNEUROSCI.13-03-01097.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  33. Vorhees CV, Williams MT. Morris water maze: procedure for assessing spatial and relate forms of learning and memory. Nat Protoc. 2006;1:484–458. doi: 10.1038/nprot.2006.116. [DOI] [PMC free article] [PubMed] [Google Scholar]
  34. Winterfeld KT, Teuchert-Noodt G, Dawirs RR. Social environment alters both ontogeny of dopamine innervation of the medial prefrontal cortex and maturation of working memory in gerbils (Meriones unguiculatus) J Neurosci Res. 1998;52:201–209. doi: 10.1002/(SICI)1097-4547(19980415)52:2<201::AID-JNR8>3.0.CO;2-E. [DOI] [PubMed] [Google Scholar]

Articles from Interdisciplinary Toxicology are provided here courtesy of Slovak Toxicology Society SETOX & Institute of Experimental Pharmacology and Toxicology, Slovak Academy of Sciences

RESOURCES