Home A study of effect of Centella asiatica on oxidative markers in the hippocampus of offsprings born to alcohol-fed pregnant rats and the correlation with their cognitive functions
Article
Licensed
Unlicensed Requires Authentication

A study of effect of Centella asiatica on oxidative markers in the hippocampus of offsprings born to alcohol-fed pregnant rats and the correlation with their cognitive functions

  • Mitha K.V. ORCID logo , Saraswati Jaiswal Yadav ORCID logo and Ganaraja Bolumbu ORCID logo EMAIL logo
Published/Copyright: May 12, 2021

Abstract

Objectives

Alcohol consumption causes several harmful effects on the organs, which is hugely understated. Many deformities occur in the fetus when pregnant mothers indulge in alcoholism. Alcohol is a known teratogen, hence organ formation, particularly development of parts brain critical for cognitive function may be affected. The oxidative brain damage also could contribute to reduced cognitive efficiency of brain exposed to alcohol. In this study, effect of Centella asiatica in relieving the oxidative brain damage in offspring of alcohol fed mother rats was evaluated.

Methods

In this study we fed alcohol (5 g/kg body weight, 30% w/v) to a group of pregnant Wistar rats during gestation period, and another group served as control. Four groups of rats (n = 6 each) were selected from the offspring of these mother rats. The groups were, control, positive (treated) control, untreated and treated from alcohol-fed mother. Their cognitive parameters were tested in water maze, shuttle box and compared. Further their oxidative status was evaluated by estimating malondialdehyde (MDA), protein carbonyl, total antioxidants and glutathione reductase (GSH) in hippocampus.

Results

The results suggested that there was significantly high cognitive performance in maze test and shuttle box memory retention in rats treated with C. asiatica water extract and the antioxidant levels were high in their hippocampus.

Conclusions

The outcome of the study suggested that C. asiatica produced beneficial effects in reversing the alcohol induced brain damage in pregnancy.


Corresponding author: Dr. Ganaraja Bolumbu, PhD, Additional Professor, Department of Physiology, Kasturba Medical College, Mangalore, Manipal Academy of Higher Education, Manipal, Karnataka, India, Phone: +91 9449642150, E-mail:

Acknowledgments

We acknowledge the support and facilities provided by the Kasturba Medical College, Mangalore, Manipal Academy of higher education, Manipal, Karnataka, India.

  1. Research funding: None declared.

  2. Author contributions: All authors have accepted responsibility for the entire content of this manuscript and approved its submission.

  3. Competing interests: Authors state no conflict of interest.

  4. Informed consent: Informed consent was obtained from all individuals included in this study.

  5. Ethical approval: Institutional Ethical Committee for animal experimentation has approved the study.

References

1. Jaffer, Z, Nelson, M, Beighton, P. Bone fusion in the fetal alcohol syndrome. J Bone Joint Surg Br 1981;63B:569–71. https://doi.org/10.1302/0301-620X.63B4.7197678.Search in Google Scholar

2. Nyquist Battie, C, Uphoff, C, Cole, TB. Maternal alcohol consumption: effect on skeletal muscle development in guinea pig offspring. Alcohol 1987;4:11–6. https://doi.org/10.1016/0741-8329(87)90053-x.Search in Google Scholar

3. Loser, H, Pgeferkorn, JR, Themann, H. Alcohol in pregnancy and fetal heart damage. Klin Pädiatr 1992;204:335–9. https://doi.org/10.1055/s-2007-1025368.Search in Google Scholar

4. Lemoine, P, Harousseau, H, Borteyru, JP, Menuet, JC. Children of alcoholic parents-observed anomalies: discussion of 127 cases. Ther Drug Monit 2003;25:132–6. https://doi.org/10.1097/00007691-200304000-00002.Search in Google Scholar

5. Jones, KL, Smith, DW. Recognition of the fetal alcohol syndrome in early infancy. Lancet 1973;2:999–1001. https://doi.org/10.1016/s0140-6736(73)91092-1.Search in Google Scholar

6. Jones, KL, Smith, DW, Ulleland, CN, Streissguth, P. Pattern of malformation in offspring of chronic alcoholic mothers. Lancet 1973;1:1267–71. https://doi.org/10.1016/s0140-6736(73)91291-9.Search in Google Scholar

7. Benegal, V, Nayak, M, Murthy, P, Chandra, P, Gururaj, G. Women and alcohol use in India. In: Obot, IS, Room, R, editors. Alcohol, gender and drinking problems (GENACIS): perspectives from low and middle income countries. Geneva: World Health Organization; 2005. pp. 89–123.Search in Google Scholar

8. Mohan, D, Anita, C, Ray, R, Sethi, H. Alcohol consumption in India; a cross sectional study. In: World Health Organization. Management of substance dependence team (‎2001)‎. Surveys of drinking patterns and problems in seven developing countries. World Health Organization; 2001:103–14 pp. https://apps.who.int/iris/handle/10665/66811.Search in Google Scholar

9. Miller, MW. Migration of cortical neurons is altered by gestational exposure to ethanol. Alcohol Clin Exp Res 1993;17:304–14. https://doi.org/10.1111/j.1530-0277.1993.tb00768.x.Search in Google Scholar PubMed

10. Miller, MW. Limited ethanol exposure selectively alters the proliferation of precursor cells in the cerebral cortex. Alcohol Clin Exp Res 1996;20:139–43. https://doi.org/10.1111/j.1530-0277.1996.tb01056.x.Search in Google Scholar PubMed

11. Ikonomidou, C, Bittigau, P, Ishimaru, MJ, Wozniak, DF, Koch, C, Genz, K, et al.. Ethanol-induced apoptotic neurodegeneration and fetal alcohol syndrome. Science 2000;287:1056–60. https://doi.org/10.1126/science.287.5455.1056.Search in Google Scholar PubMed

12. Popova, EN. Ultrastructure of neurons of the sensory motor cortex in the progeny of rats receiving alcohol during pregnancy. Neurosci Behav Physiol 1989;19:433–9. https://doi.org/10.1007/bf01197878.Search in Google Scholar

13. Berman, RF, Hannigan, JH. Effects of prenatal alcohol exposure on the hippocampus: spatial behavior, electrophysiology and neuroanatomy. Hippocampus 2000;10:94–110. https://doi.org/10.1002/(sici)1098-1063(2000)10:1<94::aid-hipo11>3.0.co;2-t.10.1002/(SICI)1098-1063(2000)10:1<94::AID-HIPO11>3.0.CO;2-TSearch in Google Scholar

14. Green, CR, Kobus, SM, Ji, Y, Bennett, BM, Reynolds, JN, Brien, JF. Chronic prenatal ethanol exposure increases apoptosis in the hippocampus of the term fetal guinea pig. Neurotoxicol Teratol 2005;27:871–81. https://doi.org/10.1016/j.ntt.2005.07.006.Search in Google Scholar

15. Jonas, P, Lisman, J. Structure, function, and plasticity of hippocampal dentate gyrus microcircuits. Front Neural Circ 2014;8:107. https://doi.org/10.3389/fncir.2014.00107.Search in Google Scholar

16. Cameron, HA, McKay, RD. Adult neurogenesis produces a large pool of new granule cells in the dentate gyrus. J Comp Neurol 2001;435:406–17. https://doi.org/10.1002/cne.1040.Search in Google Scholar

17. Clements, KM, Girard, TA, Ellard, CG, Wainwright, PE. Short-term memory impairment and reduced hippocampal c-Fos expression in an animal model of fetal alcohol syndrome. Alcohol Clin Exp Res 2005;29:1049–59. https://doi.org/10.1097/01.alc.0000171040.82077.e.Search in Google Scholar

18. Richardson, DP, Byrnes, ML, Brien, JF, Reynolds, JN, Dringenberg, HC. Impaired acquisition in the water maze and hippocampal long-term potentiation after chronic prenatal ethanol exposure in the guinea-pig. Eur J Neurosci 2002;16:1593–8. https://doi.org/10.1046/j.1460-9568.2002.02214.x.Search in Google Scholar

19. Astley, SJ, Aylward, EH, Olson, HC, Kerns, K, Brooks, A, Coggins, TE, et al.. Magnetic resonance imaging outcomes from a comprehensive magnetic resonance study of children with fetal alcohol spectrum disorders. Alcohol Clin Exp Res 2009;33:1671–89. https://doi.org/10.1111/j.1530-0277.2009.01004.x.Search in Google Scholar

20. Malisza, KL, Allman, AA, Shiloff, D, Jakobson, L, Longstaffe, S, Chudley, AE. Evaluation of spatial working memory function in children and adults with fetal alcohol spectrum disorders: a functional magnetic resonance imaging study. Pediatr Res 2005;58:1150–7. https://doi.org/10.1203/01.pdr.0000185479.92484.a1.Search in Google Scholar

21. Hamby-Mason, R, Chen, JJ, Schenker, S, Perez, A, Henderson, GI. Catalase mediates acetaldehyde formation from ethanol in fetal and neonatal rat brain. Alcohol Clin Exp Res 1997;21:1063–72. https://doi.org/10.1111/j.1530-0277.1997.tb04255.x.Search in Google Scholar

22. Kotch, LE, Chen, SY, Sulik, KK. Ethanol-induced teratogenesis: free radical damage as a possible mechanism. Teratology 1995;52:128–36. https://doi.org/10.1002/tera.1420520304.Search in Google Scholar

23. Yazgan, ÜC, Elbey, B, Kuş, S, Baykal, B, Keskin, I, Yılmaz, A, et al.. Effect of caffeic acid phenethyl ester on oxidant and anti-oxidant status of liver and serum in a rat model with acute methanol intoxication. Ir J Med Sci 2017;186:519–23. Epub 2016 Apr 30. https://doi.org/10.1007/s11845-016-1462-2.Search in Google Scholar

24. Mitha, KV, Yadav, S, Mayannavar, S, Ganaraja, B. Effect of alcohol consumption in pregnancy on pup quality, exploratory behaviour, memory retention in Wistar rats. IJABPT 2014;5:73–8.Search in Google Scholar

25. Mitha, KV, Yadav, S, Ganaraja, B. Improvement in cognitive parameters among offspring born to alcohol fed female Wistar rats following long term treatment with Centella asiatica. Indian J Physiol Pharmacol 2016;60:167–73.Search in Google Scholar

26. Acharya, YT. Caraka, Āyurveda Dīpikā Vyakhyā. Varanasi: Chaukhambha Prakashan; 2011. Re-print 2011.Search in Google Scholar

27. Sivarajan, VV, Balachandran, I. Ayurvedic drugs and their plant sources. New Delhi: Oxford and IBH Publishing; 1994. p. 289–90.Search in Google Scholar

28. Dash, PK, Mistry, IU, Rao, AR, Patel, KS. Role of Medhya Rasayana in school children. Ayu 1996;12:15.Search in Google Scholar

29. Rahman, M, Hossain, S, Rahaman, A, Fatima, N, Nahar, T, Uddin, B, et al.. Antioxidant activity of Centella asiatica (Linn.) urban: impact of extraction solvent polarity. J Pharmacogn Phytochem 2013;1:27.Search in Google Scholar

30. Babu, TD, Kuttan, G, Padikkala, J. Cytotoxic and anti-tumour properties of certain taxa of Umbelliferae with special reference to Centella asiatica (L.) Urban. J Ethnopharmacol 1995;48:53–7. https://doi.org/10.1016/0378-8741(95)01284-k.Search in Google Scholar

31. Shukla, A, Rasik, AM, Dhawan, BN. Asiaticoside-induced elevation of antioxidant levels in healing wounds. Phytother Res 1999;13:50–4. https://doi.org/10.1002/(sici)1099-1573(199902)13:1<50::aid-ptr368>3.0.co;2-v.10.1002/(SICI)1099-1573(199902)13:1<50::AID-PTR368>3.0.CO;2-VSearch in Google Scholar

32. Kumar, A, Dogra, S, Prakash, A. Neuroprotective effects of Centella asiatica against intracerebroventricular colchicine-induced cognitive impairment and oxidative stress. Int J Alzheimers Dis 2009;2009:1–8. https://doi.org/10.4061/2009/972178.Search in Google Scholar

33. Ochiogu, IS, Uchendu, CN, Ihedioha, JI. A new and simple method of confirmatory detection of mating in Albino rats (Rattus norvegicus). Anim Res Int 2006;3:527–30.10.4314/ari.v3i3.40784Search in Google Scholar

34. Murawski, NJ, Klintsova, AY, Stanton, ME. Neonatal alcohol exposure and the hippocampus in developing male rats: effects on behaviorally induced CA1 c-Fos expression, CA1 pyramidal cell number, and contextual fear conditioning. Neuroscience 2012;206:89–99. https://doi.org/10.1016/j.neuroscience.2012.01.006.Search in Google Scholar

35. Gupta, YK, Veerendara, MH, Sreivastava, AK. Effect of Centella asiatica on pentylenetrazole-induced kindling, cognition and oxidative stress in rats. Pharmacol Biochem Behav 2003;74:579–85. https://doi.org/10.1016/s0091-3057(02)01044-4.Search in Google Scholar

36. Harborne, JB. Phytochemical methods. New Delhi: Springer (India) Pvt. Ltd; 2005:17 p.Search in Google Scholar

37. Madhyastha, S, Somayaji, SN, Bairy, KL, Prakash, MP. Neuroprotective effect of Centella asiatica leaf extract treatment on cognition and hippocampal morphology against prenatal stress. Thai J Physiol Sci 2007;20:79–88.Search in Google Scholar

38. Morris, R. Developments of a water-maze procedure for studying spatial learning in the rat. J Neurosci Methods 1984;11:47–60. https://doi.org/10.1016/0165-0270(84)90007-4.Search in Google Scholar

39. Cherian, SB, Bairy, KL, Rao, MS. Chronic prenatal restraint stress induced memory impairment in passive avoidance task in post weaned male and female Wistar rats. Indian J Exp Biol 2009;47:893–9.Search in Google Scholar

40. Ohkawa, H, Ohishi, N, Yagi, K. Assay for lipid peroxides in animal tissues by thiobarbituric acid reaction. Anal Biochem 1979;95:351–8. https://doi.org/10.1016/0003-2697(79)90738-3.Search in Google Scholar

41. Levine, RL, Garland, D, Oliver, CN, Amiei, A, Climent, I, Lenz, AG. Determination of carbonyl content in oxidatively modified proteins. Methods Enzymol 1990;86:464–78. https://doi.org/10.1016/0076-6879(90)86141-h.Search in Google Scholar

42. Benzie, IFF, Strain, JJ. The ferric reducing ability of plasma (FRAP) as a measure of “antioxidant power”: the FRAP assay. Anal Biochem 1996;239:70–6. https://doi.org/10.1006/abio.1996.0292.Search in Google Scholar

43. Butler. Estimation of glutathione content of RBC and whole blood. J Lab Clin Med 1963;61:882.Search in Google Scholar

44. Lowry, OH, Rosenbrough, NJ, Farr, AL, Randall, RJ. Protein measurement with folin phenol reagent. J Biol Chem 1951;193:265–75. https://doi.org/10.1016/s0021-9258(19)52451-6.Search in Google Scholar

45. Salami, M, Aghanouri, Z, Ali Akbar Rashidi, BS, Keshavarz, M. Prenatal alcohol exposure and dysfunction of hippocampal formation in cognition. Iran J Reprod Med 2004;2:43–50.Search in Google Scholar

46. Lei, A, Yang, Z, Zhang, T. Imbalanced synaptic plasticity induced spatial cognition impairment in male offspring rats treated with chronic prenatal ethanol exposure. Alcohol Clin Exp Res 2013;37:763–70. https://doi.org/10.1111/acer.12040.Search in Google Scholar PubMed

47. Henderson, GI, Devi, BG, Perez, A, Schenker, S. In utero ethanol exposure elicits oxidative stress in the rat fetus. Alcohol Clin Exp Res 1995;19:714–20. https://doi.org/10.1111/j.1530-0277.1995.tb01572.x.Search in Google Scholar

48. Jamshidi-Kia, F, Wibowo, JP, Elachouri, M, Masumi, R, Salehi Jouneghani, A, Abolhassanzadeh, Z, et al.. Battle between plants as antioxidants with free radicals in human body. J Herbmed Pharmacol 2020;9:191–9. https://doi.org/10.34172/jhp.2020.25.Search in Google Scholar

49. Goldman, R, Claycamp, GH, Sweetland, MA, Sedlov, AV, Tyurin, VA, Kisin, ER, et al.. Myeloperoxidase-catalyzed redox-cycling of phenol promotes lipid peroxidation and thiol oxidation in HL-60 cells. Free Radic Biol Med 1999;27:1050–63. https://doi.org/10.1016/S0891-5849(99)00140-9.Search in Google Scholar

50. Veerendra Kumar, MH, Gupta, YK. Effect of Centella asiatica on cognition and oxidative stress in an intracerebroventricular streptozotocin model of Alzheimer’s disease in rats. Clin Exp Pharmacol Physiol 2003;30:336–42. https://doi.org/10.1046/j.1440-1681.2003.03842.x.Search in Google Scholar PubMed

51. Krishnamurthy, RG, Senut, MC, Zemke, D, Min, J, Frenkel, MB, Greenberg, EJ, et al.. Asiatic acid, a pentacyclic triterpene from Centella asiatica, is neuroprotective in a mouse model of focal cerebral ischemia. J Neurosci Res 2009;87:2541–50. https://doi.org/10.1002/jnr.22071.Search in Google Scholar PubMed PubMed Central


Supplementary Material

The online version of this article offers supplementary material (https://doi.org/10.1515/jcim-2020-0472).


Received: 2020-11-23
Accepted: 2021-03-26
Published Online: 2021-05-12

© 2021 Walter de Gruyter GmbH, Berlin/Boston

Articles in the same Issue

  1. Frontmatter
  2. Reviews
  3. Evidence implementation among complementary medicine practitioners: a meta-summary
  4. Phytochemical: a treatment option for heavy metal induced neurotoxicity
  5. The effects of curcumin-containing supplementations on inflammatory markers and lipid profiles in patients with chronic kidney diseases: a systematic review and meta-analysis of randomized controlled trials
  6. A systematic review on traditional medicinal Animal’s parts and products used for the treatment of respiratory tract disorders in Ethiopia
  7. Review on nutraceuticals: phase transition from preventive to protective care
  8. A study of effect of Centella asiatica on oxidative markers in the hippocampus of offsprings born to alcohol-fed pregnant rats and the correlation with their cognitive functions
  9. Anxiogenic and anxiolytic effects of memantine injected into the ventral hippocampus in male stressed mice
  10. Research Articles
  11. Comparison of antithyroid effects and hepatic complications of methimazole with catechin and its nanoencapsulation form in adult male rats
  12. Almond oil restores blood parameters, liver function, blood and liver antioxidants and DNA, and liver histology more efficiently than olive oil in favism
  13. Highly efficient microencapsulation of phytonutrients by fractioned cellulose using biopolymer complexation technology
  14. Ocimum basilicum alleviates blood glucose, lipid profile and iNOS in diabetes gestational rat model
  15. Blood pressure and blood sugar-lowering effects of purified gambir on diabetic hypertensive Wistar Kyoto rats
  16. Assessment of anti-inflammatory and antioxidant activity of quercetin–rutin blend (SophorOx™) – an invitro cell based assay
  17. Subchronic toxicological evaluation of EnXtra™ (standardised extract of Alpinia galanga rhizome) in rats
  18. Ficus glumosa Del. reduces phenylhydrazine-induced hemolytic anaemia and hepatic damage in Wistar rats
  19. Screening of anti-cancerous potential of classical Raudra rasa and modified Raudra rasa modified with hiraka bhasma (nanodiamond) through FTIR & LC-MS analysis
  20. Aqueous extract of Pedalium murex D. Royen ex L. leafy stem protects against lead induced testicular toxicity in Wistar rats
  21. Intrahippocampal co-administration of nicotine and O-acetyl-L-carnitine prevents the H-89-induced spatial learning deficits in Morris water maze
  22. Developmental effects of early-life stress on dopamine D2 receptor and proteins involved in noncanonical D2 dopamine receptor signaling pathway in the prefrontal cortex of male rats
  23. Probiotic administration enhanced antitrypanosomal effects of diminazene aceturate in dogs experimentally infected with Trypanosoma brucei brucei
  24. Acacia arabica (Lam.) Willd. On osteoblastogenesis, osteoblast proliferation, osteoclastic activity, and bone calcium mineralization
  25. GC-MS analysis of curculigo orchiodes and medicinal herbs with cytotoxic, hepatoprotective attributes of ethanolic extract from Indian origin
  26. Biochemical and histopathological evaluation of liver, kidney, and pancreas in normal Sprague Dawley rats administered aqueous extract of beetroot (Beta vulgaris)
  27. The effectiveness of emotional freedom techniques (EFT) on depression of postmenopausal women: a randomized controlled trial
  28. The formulation and efficacy of topical Dorema ammoniacum in treating Melasma: a randomized double-blind, placebo-controlled trial
  29. Impact of inhalation aromatherapy with Damask Rose (Rosa damascena) on stress, anxiety and hemodynamic parameters of patients undergoing coronary angiography: a single blind randomized clinical trial
  30. Hydro-alcoholic extract of Morus nigra reduces fasting blood glucose and HbA1c% in diabetic patients, probably via competitive and allosteric interaction with alpha-glucosidase enzyme; a clinical trial and in silico analysis
  31. Prophylactic management of radiation-induced mucositis using herbal mouthwash in patients with head and neck cancer: an assessor-blinded randomized controlled trial
  32. Implementation science in New Zealand naturopathic practice: a cross-sectional study
  33. Issues of mindfulness implementation for oncology caregivers
  34. Immediate effect of cold mud pack therapy on autonomic variables in primary hypertensive individuals: a randomized trial
  35. Effect of a Persian metabolic diet on the functional dyspepsia symptoms in patients with postprandial distress syndrome: a randomized, double-blind clinical trial
Downloaded on 20.9.2025 from https://www.degruyterbrill.com/document/doi/10.1515/jcim-2020-0472/html
Scroll to top button