Skip to main content

Assessing the Anxiolytic Properties of Taurine-Derived Compounds in Rats Following Developmental Lead Exposure: A Neurodevelopmental and Behavioral Pharmacological Pilot Study

  • Conference paper
  • First Online:
Taurine 11

Abstract

Lead (Pb2+) is a developmental neurotoxicant that causes alterations in the brain’s excitation-to-inhibition (E/I) balance. By increasing chloride concentration through GABA-ARs, taurine serves as an effective inhibitory compound for maintaining appropriate levels of brain excitability. Considering this pharmacological mechanism of taurine facilitated inhibition through the GABA-AR, the present pilot study sought to explore the anxiolytic potential of taurine derivatives. Treatment groups consisted of the following developmental Pb2+-exposures: Control (0 ppm) and Perinatal (150 ppm or 1000 ppm lead acetate in the drinking water). Rats were scheduled for behavioral tests between postnatal days (PND) 36–45 with random assignments to either solutions of Saline, Taurine, or Taurine Derived compounds (i.e., TD-101, TD-102, or TD-103) to assess the rats’ responsiveness to each drug in mitigating the developmental Pb2+-exposure through the GABAergic system. Long Evans Hooded rats were assessed using an Open Field (OF) test for preliminary locomotor assessment. Approximately 24-h after the OF, the same rats were exposed to the Elevated Plus Maze (EPM) and were given an i.p. injection of 43 mg/Kg of the Saline, Taurine, or TD drugs 15-min prior to testing. Each rat was tested using the random assignment method for each pharmacological condition, which was conducted using a triple-blind procedure. The OF data revealed that locomotor activity was unaffected by Pb2+-exposure with no gender differences observed. However, Pb2+-exposure induced an anxiogenic response in the EPM, which interestingly, was ameliorated in a gender-specific manner in response to taurine and TD drugs. Female rats exhibited more anxiogenic behavior than the male rats; and as such, exhibited a greater degree of anxiety that were recovered in response to Taurine and its derivatives as a drug therapy. The results from the present psychopharmacological pilot study suggests that Taurine and its derivatives could provide useful data for further exploring the pharmacological mechanisms and actions of Taurine and the associated GABAergic receptor properties by which these compounds alleviate anxiety as a potential behavioral pharmacotherapy for treating anxiety and other associated mood disorders.

This is a preview of subscription content, log in via an institution to check access.

Access this chapter

Chapter
USD 29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 329.00
Price excludes VAT (USA)
  • Available as EPUB and PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD 419.00
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info
Hardcover Book
USD 449.99
Price excludes VAT (USA)
  • Durable hardcover edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

Abbreviations

Pb2+:

Lead

TD:

Taurine derivatives

E/I:

Excitation-to-inhibition

BLL:

Blood lead levels

GAD:

Glutamic acid decarboxylase

PND:

Postnatal day

EDTA:

Ethylenediaminetetracetic acid

ASV:

Anodic stripping voltammetry

OF:

Open field

EPM:

Elevated plus maze

OTC:

Open-to-closed ratio

References

  • Agency for Toxic Substances and Disease Registry (ATSDR) (2007) Toxicological profile for lead. U.S. Department of Health and Human Services, pp 1–582. Retrieved July 7th, 2018 from https://www.atsdr.cdc.gov/toxprofiles/tp13.pdf

  • Barbosa F Jr, Tanus-Santos JE, Gerlach RF, Parsons PJ (2005) A critical review of biomarkers used for monitoring human exposure to lead: advantages, limitations, and future needs. Environ Health Perspect 113(12):1669–1674

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Bellinger DC (2008) Very low lead exposures and children’s neurodevelopment. Curr Opin Pediatr 20(2):172–177

    Article  PubMed  Google Scholar 

  • Bellinger DC, Dietrich KN (1994) Low-level lead exposure and cognitive function in children. Pediatr Ann 23:600–605

    Article  CAS  PubMed  Google Scholar 

  • Bellinger DC, Needleman HL (2003) Intellectual impairment and blood lead levels. N Engl J Med 349:5000

    Google Scholar 

  • Ben-Ari Y (2002) Excitatory actions of GABA during development: the nature or the nurture. Nat Rev Neurosci 9:728–739

    Article  Google Scholar 

  • Ben-Ari Y, Khalilov I, Kahle KT, Cherubini E (2012) The GABA excitatory/inhibitory shift in brain maturation and neurological disorders. Neuroscientist 18:1–20

    Article  Google Scholar 

  • Bergdhal IA, Skerfving S (2008) Biomonitoring of lead exposures--alternatives to blood. J Toxicol Environ Health A 71(18):1235–1243

    Article  Google Scholar 

  • Bleecker ML, Lingren KN, Ford PD (1997) Differential contribution of current and cumulative indices of lead dose to neuropsychological performance by age. Neurology 48(3):639–645

    Article  CAS  PubMed  Google Scholar 

  • Brody DJ, Prikle JL, Kramer RA, Flegal KM, Matte TD, Gunter EW, Paschal DC (1994) Blood levels in the US poplation: phase 1 of the Third National Health and Nutrition Examination Survey (NHANES III, 1988–1991). JAMA 272:2277–2283

    Article  Google Scholar 

  • Canfield RL, Henderson CR Jr, Cory-Slechta DA, Cox C, Jusko TA, Lanphear BP (2003) Intellectual impairment in children with blood lead concentrations below 10 microgram per deciliter. N Engl J Med 348:1517–1526

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Chen A, Dietrich KN, Huo X, Ho SM (2011) Developmental neurotoxicants in E-waste: an emerging health concern. Environ Health Perspect 119(4):431–438

    Article  PubMed  Google Scholar 

  • Dietrich KN, Ware JH, Salganik M, Radcliffe J, Rogan WJ, Rhoads GG, Fay ME, Davoli CT, Denckla MB, Bornschein RL, Schwarz D, Dockkery DW, Adubato S, Jones RL (2004) Effect of chelation therapy on the neuropsychological and behavioral development of lead-exposed children after school entry. Pediatrics 114(1):19–26

    Article  PubMed  Google Scholar 

  • Edwards M, Triantafyllidou S, Best D (2009) Elevated lead in young children due to lead-contaminated drinking water: Washington, DC, 2001–2004. Environ Sci Technol 43(5):1618–1623

    Article  CAS  PubMed  Google Scholar 

  • El Idrissi A (2008) Taurine improves learning and retention in aged mice. Neurosci Lett 436:19–22

    Article  PubMed  Google Scholar 

  • El Idrissi A (2011) Functional consequences of taurine interaction with the GABAergic system. Amino Acids 41:S83

    Google Scholar 

  • El Idrissi A, L’Amoreaux WJ (2008) Selective resistance of taurine-fed mice to isoniazide-potentiated seizures: in-vivo functional test for the activity of glutamic acid decarboxylase. Neuroscience 156(3):693–699

    Article  PubMed  Google Scholar 

  • El Idrissi A, Messing J, Scalia J, Trenkner E (2003) Prevention of epileptic seizures through taurine. In: Lombardini JB, Schaffer SW, Azuma J (eds) Taurine 5 beginning the 21st century. Kluwer Press, New York. Adv Exp Med Biol 526: 515–525

    Google Scholar 

  • El Idrissi A, Boukarrou L, Heany W, Malliaros G, Sangdee C, Neuwirth LS (2009) Effects of taurine on anxiety-like and locomotor behavior of mice. Taurine 7, Adv Exp Med Biol 643:207–215

    Article  Google Scholar 

  • El Idrissi A, Iskra BS, Neuwirth LS (2011) Neurobehavioral effects of taurine in fragile X syndrome. In: El Idrissi A, L’Amoreaux WJ (eds) Taurine 8: taurine in health and disease, vol 644. Springer Press, New York, pp 306–345

    Google Scholar 

  • El Idrissi A, Shen CH, L’Amoreaux WJ (2013) Neuroprotective role of taurine during aging. Amino Acids 45(4):735–750

    Article  PubMed  Google Scholar 

  • Eneh OC, Agunwamba JC (2011) Managing hazardous wastes in Africa: recyclability of lead from E-waste materials. J Appl Sci 11(17):3215–3220

    Article  CAS  Google Scholar 

  • Gilbert SG, Weiss B (2006) A rationale for lowering the blood lead action level from 10 to 2 μg/dL. Neurotoxicology 27(5):693–701

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Grandjean P, Hertz KT (2015) Trace elements as paradigms of developmental neurotoxicants: lead, methylmercury, and arsenic. J Trace Elem Med Biol 31:130–134

    Article  CAS  PubMed  Google Scholar 

  • Guo Y, Huo X, Li Y, Wu K, Liu J, Huang J, Zheng G, Xiao Q, Yang H, Wang Y, Chen A, Xu X (2010) Monitoring of lead, cadmium, chromium and nickel in placenta from an E-waste recycling town in China. Sci Total Environ 408(16):3113–3117

    Article  CAS  PubMed  Google Scholar 

  • Hernberg S (2000) Lead poisoning in a historical perspective. Am J Ind Med 38(3):244–254

    Article  CAS  PubMed  Google Scholar 

  • Huo X, Peng L, Xu X, Zheng L, Qui B, Qi Z, Zhang B, Han D, Pio Z (2007) Elevated blood lead levels of children in Guiyu, and electronic waste recycling town in China. Environ Health Perspect 115(7):1113–1117

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Krieg EF Jr, Chrislip DW, Crespo CJ, Brightwell WS, Ehrenberg RL, Otto DA (2005) The relationship between blood lead levels and neurobehavioral test performance in NHANES III and related occupational studies. Public Health Rep 120(3):240–251

    Article  PubMed  PubMed Central  Google Scholar 

  • L’Amoreaux WJ, Marsillo A, El Idrissi A (2010) Pharmacological characterization of GABAA receptors in taurine-fed mice. J Biomed Sci 17(1–5):S14

    Article  PubMed  PubMed Central  Google Scholar 

  • Laidlaw MAS, Taylor MP (2011) Potential for childhood lead poisoning in the inner cities of Australia due to exposure to lead in soil dust. Environ Pollut 159(1):1–9

    Article  CAS  PubMed  Google Scholar 

  • Lanphear BP, Dietrich K, Auinger P, Cox C (2000) Cognitive deficits associated with blood lead concentrations < 10 microg/dL in US children and adolescents. Public Health 115:521–529

    CAS  PubMed  PubMed Central  Google Scholar 

  • Leung AOW, Duzgoren-Aydin NS, Cheung KC, Wong MH (2008) Heavy metals concentrations of surface dust from E-waste recycling and its human health implications in southeast China. Environ Sci Technol 42(7):2674–2680

    Article  CAS  PubMed  Google Scholar 

  • Lidsky TI, Schneider JS (2006) Adverse effects of childhood lead poisoning: the clinical neuropsychological perspective. Environ Res 100:284–293

    Article  CAS  PubMed  Google Scholar 

  • Needleman HL (2004) Lead poisoning. Annu Rev Med 55:209–222

    Article  CAS  PubMed  Google Scholar 

  • Needleman HL, Gatsonis CA (1990) Low-level lead exposure and the IQ of children. A meta-analysis of modern studies. J Am Med Assoc 263:673–678

    Article  CAS  Google Scholar 

  • Neuwirth LS (2014) The characterization of Pb2+ toxicity in rat neural development: an assessment of Pb2+ effects on the GABA-shift in neural networks and implications for learning and memory disruption. UMI Proquest Dissertation & Theses 3612469. DAI/B 75-06(E), Apr 2014

    Google Scholar 

  • Neuwirth LS (2018) Resurgent lead poisoning and renewed public attention towards environmental social justice issues: a review of current efforts and call to revitalize primary and secondary lead poisoning prevention for pregnant women, lactating mothers, and children within the U.S. Int J Occup Environ Health, (in press)

    Google Scholar 

  • Neuwirth LS, Volpe NP, El Idrissi A (2013) Taurine effects on emotional learning and memory in aged mice: neurochemical alterations and differentiation in auditory cued fear and context conditioning. In: El Idrissi A, L’Amoreaux WJ (eds) Taurine 8: the nervous system, immune system, diabetes, and the cardiovascular system. Springer, New York. Adv Exp Med Biol 775: 195–214

    Google Scholar 

  • Neuwirth LS, Volpe NP, Corwin C, Ng S, Madan N, Ferraro AM, Furman Y, El Idrissi A (2017) Taurine recovery of learning deficits induced by developmental Pb2+ exposure. In: Lee DH, Shaffer S, Park E, Kim HW (eds) Taurine 10: 975: 39–55. https://doi.org/10.1007/978-94-024-1079-2_4

    Google Scholar 

  • Neuwirth LS, Phillips GR, El Idrissi A (2018) Perinatal Pb2+ exposure alters the expression of genes related to the neurodevelopmental GABA-shift in postnatal rats. J Biomed Sci 25(45):1–11. https://doi.org/10.1186/s12929-018-0450-4

    Article  CAS  Google Scholar 

  • Neuwirth LS, Masood S, Anderson DW, Schneider JS (2019a) The attention set-shifting test is sensitive for revealing sex-based impairments in executive functions following developmental lead exposure in rats. Behav Brain Res 366:126–134

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Neuwirth LS, Kim Y, Barrera ED, Jo C, Chrisphonte JM, Hameed N, Rubi S, Dacius TF Jr, Skeen JC, Bonitto JR, Khairi E, Iqbal A, Ahmed I, Masood S, Tranquille B, Thiruverkadu V (2019b) Early neurodevelopmental exposure to low lead levels induces frontoexecutive dysfunctions that are recovered by taurine co-treatment in the rat attention set-shift test: implications for taurine as a psychopharmacotherapy against neurotoxicants. In: Hu J, Yang J, Schaffer SW (eds) Taurine 11. (in press)

    Google Scholar 

  • Rentschler G, Broberg K, Lundh T, Skerfving S (2012) Long-term lead elimination from plasma and whole blood after poisoning. Int Arch Occup Environ Health 85(3):311–316

    Article  CAS  PubMed  Google Scholar 

  • Rogan WJ, Dietrich KN, Ware JH, Dockery DW, Salganki M, Radcliffe J, Jones RL, Ragan NB, Chisolm JJ Jr, Rhoads GG (2001) The effect of chelation therapy with succimer on neuropsychological development in children exposed to lead. N Engl J Med 344:1421–1426

    Article  CAS  PubMed  Google Scholar 

  • Santora A, Neuwirth LS, L’Amoreaux WJ, El Idrissi A (2013) The effects of chronic taurine supplementation on motor learning. In: El Idrissi A, L’Amoreaux WJ (eds) Taurine 8: physiological roles and mechanisms of action, vol 775. Springer, New York, pp 177–185. https://doi.org/10.1007/978-1-4614-6130-2_15

    Chapter  Google Scholar 

  • Schütz A, Bergdhal IA, Ekholm A, Skerfving S (1996) Measurement by ICP-MS of lead in plasma and whole blood of lead workers and controls. Occup Environ Med 53(11):736–740

    Article  PubMed  PubMed Central  Google Scholar 

  • Schwartz J (1994) Low-level lead exposure and children’s IQ: a meta-analysis and search for a threshold. Environ Res 65:42–55

    Article  CAS  PubMed  Google Scholar 

  • Shinkuma T, Huong NTM (2009) The flow of E-waste material in the Asian region and a reconsideration of international trade policies on E-Waste. Environ Impact Assess Rev 29(1):25–31

    Article  Google Scholar 

  • U.S. Department of Health and Human Services (2007) Public health service agency for toxic substances and disease registry. http://www.atsdr.cdc.gov/toxprofiles/tp13.pdf. Accessed 7 July 2018

    Google Scholar 

  • Walf AA, Frye CA (2007) The use of the elevated plus maze as an assay of anxiety-related behavior in rodents. Nat Protoc 2(2):322–328

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Wong VCN, Ng THK, Yeung CY (1991) Electrophysiologic study in acute lead poisoning. Pediatr Neurol 7(2):133–136

    Article  CAS  PubMed  Google Scholar 

  • Yan CH, Xu J, Shen XM (2013) Childhood lead poisoning in China: challenges and opportunities. Environ Health Perspect 121(10):A294–A295

    Article  PubMed  PubMed Central  Google Scholar 

  • Yang Y, Lu XS, Li DL, Yu YJ (2013) Effects of environmental lead pollution on blood lead and sex hormone levels among occupationally exposed group in an E-waste dismantling area. Biomed Environ Sci 26(6):474–484

    PubMed  Google Scholar 

  • Zheng L, Wu K, Yan L, Zongli Q, Han D, Zhang B, Gu C, Chen G, Liu J, Chen S, Xu X, Huo X (2008) Blood lead and cadmium levels and relevant factors among children from an E-waste recycling town in China. Environ Res 108(1):15–20

    Article  CAS  PubMed  Google Scholar 

Download references

Acknowledgements

This study was supported by a SUNY Old Westbury Faculty Development grant awarded to L.S.N. We would like to thank the Co-Directors of the SUNY Old Westbury Collegiate-Science Technology Entry Program (C-STEP) Dr. Patrick Cadet and Mrs. Monique Clark for supporting underrepresented minority (URM) research students. The following URM students were supported by the C-STEP program: E.D.B, N.H., S.R., T.F.D. Jr., J.C.S., J.R.B, E.K., A.I., I.A., T.J.J., K.L., A.L.A., & B.T. Lastly, we would like to thank the Biology, Chemistry & Physics Department, and the SUNY-Neuroscience Research Institute for sharing resources and space allocations to conduct this study.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Lorenz S. Neuwirth .

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 2019 Springer Nature Singapore Pte Ltd.

About this paper

Check for updates. Verify currency and authenticity via CrossMark

Cite this paper

Neuwirth, L.S. et al. (2019). Assessing the Anxiolytic Properties of Taurine-Derived Compounds in Rats Following Developmental Lead Exposure: A Neurodevelopmental and Behavioral Pharmacological Pilot Study. In: Hu, J., Piao, F., Schaffer, S., El Idrissi, A., Wu, JY. (eds) Taurine 11. Advances in Experimental Medicine and Biology, vol 1155. Springer, Singapore. https://doi.org/10.1007/978-981-13-8023-5_69

Download citation

Publish with us

Policies and ethics