|
Page 6 of 6
Administration of unmodified ECS may lead to spinal fracture and paraplegia in a small percentage of rats. In our experience, the risk is greater in very young animals and when higher stimulus doses are used; however, old animals and those with greater muscle mass are also at risk. Administration of modified ECS is difficult. Ventilating a paralyzed rat before and after the ECS poses problems, and the use of anesthesia may enhance the ECS-induced cognitive deficits (Miller et al., 1985). While the latter may be desirable because it makes the model more representative of clinical contexts, results may actually be inconsistent. Some studies have reported less amnesia with the use of anesthesia, and even the elimination of convulsion (Fochtmann, 1994).
Making an ECS schedule representative of clinical contexts is not easy. We have observed that the administration of alternate-day ECS does not reliably induce amnesia with the models of cognition that we have studied. In this regard, models of retrograde amnesia pose particular problems. The number and frequency of the ECS administered must ideally mimic a clinical course of treatments; however, employing such a schedule of ECS risks introducing time-dependent forgetting of pre-ECS learning. We have therefore administered daily ECS, and sometimes even twice daily ECS, with the (unproven) assumption that the mechanisms of ECS-induced amnesia are similar, provided that the number and frequency of ECS do not differ too widely from clinical norms.
Care must be taken to ensure that the interval between the administration of ECS and subsequent exposure of the rat to the learning task is consonant with the aspect of memory that is being studied. Early exposure to the task is relevant to the transient, postictal cognitive effects of ECT while later exposure is relevant to the more enduring deficits.
Finally, just as learning assessments are best conducted at a fixed time of day, ECS should ideally be administered at a fixed time. This is because variations in ECS-induced seizures have been noted at various points in the diurnal cycle. These variations have been attributed to endogenous opioid levels (Oliverio et al., 1985).
Conclusion
In this article, we have briefly introduced the practice of herbal medicine in India, summarized the studies that have examined the herbal attenuation of amnestic deficits induced by ECS, and discussed the application and limitations of animal models in the context of such research. We have primarily focused on our own work and insights, and have also examined practical issues that are involved in studies of this nature. For a comprehensive review of the effects of ECS on memory and cognition, the effects of pharmacological agents on ECS-induced memory deficits, and the effect of coadministered drugs on ECS seizure properties, the reader is referred to Krueger et al. (1992) and Fochtmann (1994).
Acknowledgment: This article was supported in part by a grant from the Council for Scientific and Industrial Research (CSIR), New Delhi, India.
next: Participate In An ECT Evaluation
References
Abrams R. Electroconvulsive therapy. New York: Oxford University Press, 1997.
Alpern HP, McGaugh JL. Retrograde amnesia as a function of duration of electroshock stimulation. J Comp Physiol Psychol 1968;65:265-9.
Andrade C. Psychobiological frontiers of electroconvulsive therapy in depression: evaluation of strategies for rational prescription and reduction in morbidity. Tilak Venkoba Rao Oration. Indian J Psychiatry 1990;32: 109-30.
Andrade C. Electroconvulsive therapy: methods and results of basic science research at NIMHANS. In: Khanna S, Channabasavanna SM, Keshavan MS, eds. Methods in biological psychiatry research. New Delhi: Tata McGraw-Hill, 1995:114-38.
Andrade C, Joseph J, Chandra JS, Venkataraman BV, Naga Rani MA. ECT-induced anterograde amnesia: can the deficits be minimized? Convulsive Ther 1994a;10:59-64.
Andrade C, Raj T, Udaya HB, Chandra JS. Effect of BR-16A on alpha-2 adrenergic, dopamine autoreceptor and dopamine postsynaptic receptor functioning. Indian J Pharmacol 1994b;26:292-5.
Andrade C, Udaya HB, Chandra JS. BR-16A restricts development of ECS-induced retrograde amnesia. Biol Psychiatry 1995;37:820-2.
Andrade C, Mathews M, George V, Anil M, George J, Naga Ram MA. Lack of effect of Shankapushpi in the attenuation of ECS-induced memory deficits [Abstract]. Indian J Psychiatry 199638(2;suppl): 11.
Andrade C, Gowda S, Chaturvedi SK. Treatment of age-related cognitive decline with a herbal formulation: a double-blind study. Indian J Psychiatry 1998;40:240-6.
Andrade C, Anitha K, Moola B, Hegde R, Chandra JS. A simplified herbal formulation attenuates electroconvulsive shock-induced anterograde amnesia (Letter). J ECT 1999; 15:164-5.
Bures J, Buresova 0, Huston JP, Eds. Techniques and basic experiment for the study of brain and behavior. Amsterdam: Elsevier Scientific Publishing Company, 1976.
Cott J. U.S. efforts in natural products research. In: Koslow SH, Murthy RS, Coelho GV, eds. Decade of the brain. Rockville, MD: U.S. Department of Health and Human Services. 1995:173-83.
Cott J, Misra R, Dev S. Novel pharmacological profile of some psychoactive medicinal plant extracts. Psychopharmacol Bull 1994;30:95.
Dhawan BN. Centrally acting agents from Indian plants. In: Koslow SH, Murthy RS. Coelho GV, eds. Decade of the brain. Rockville, MD: U.S. Department of Health and Human Services, 1995:197-202.
Docter RF. The effect of electroconvulsive shock (ECS) vs. "brief stimulus therapy" (BST) on memory and nest-building in albino rats. J Comp Physiol Psychol 1957;50:100-4.
Dorfman LJ, Jarvik ME. Comparative amnesic effects of transcorneal and transpinnate ECS in mice. Physiol Behav 1968;3:815-8.
Faruqi S, Andrade C, Ramteke S, Joseph J, Venkataraman BV, Naga Rani MA. Herbal pharmacotherapy for the attenuation of ECS-induced anterograde and retrograde amnestic deficits. Convulsive Ther 1995; 11:241-7.
Fochtmann LJ. Animal studies of electroconvulsive therapy: foundations for future research. Psychopharmacol Bull 1994;30:321-444.
Gardner EL, Glick SD, Jarvik ME. ECS dissociation of learning and one-way cross-dissociation with physostigmine and scopolamine. Physiol Behav 1972;8:11-5.
Handa SS. Plants and plant products for mental health. In: Koslow SH, Murthy RS, Coelho GV, eds. Decade of the brain. Rockville, MD: U.S. Department of Health and Human Services 1995;163-71.
Himalaya Drug Company. Mentat: a monograph. Bangalore: Himalaya Drug Company, 1991.
Iyengar MA. Study of crude drugs. Manipal: Manipal Power Press, 1981.
Joseph MH, Waddington JL, eds. Working methods in neuropsychopharmacology. Manchester: Manchester University Press, 1986.
Joseph J, Venkataraman BV, Naga Ram MA, Andrade C. BR-16A protects against ECS-induced anterograde amnesia. Biol Psychiatry 1994:36:478-81.
Kirtikar KR, Basu BD. Indian medicinal plants. 2nd ed. Vols. 1 and 2. Debra Dun: Shiva Offset Press, 1993.
Kirtikar KR, Basu BD. Indian medicinal plants. 2nd ed. Vols. 3 and 4. Debra Dun: Shiva Offset Press, 1994.
Kral PA, Beggerly HD. Electroconvulsive shock impedes association formation. Conditioned taste aversion paradigm. Physiol Behav 1973: 10: 145-7.
Krueger RB, Sackeim HA, Gamzu ER. Pharmacological treatment of the cognitive side effects of ECT: a review. Psychopharmacol Bull 1992:28:409-24.
Le Bars PL, Katz MM, Berman N, Itil TM, Freedman AM, Schatzberg AF, for the North American EGb Study Group. A placebo-controlled. double-blind, randomized trial of an extract of Ginkgo Biloba for dementia. JAMA 1997:278:1327-32.
Linde K, Ramirez G, Mulrow CD. Pauls A, Weidenhammer W, Melchart D. St. John's Wort for depression-an overview and meta-analysis of randomized clinical trials. BMJ 1996:313:253-8.
Miller AL, Faber RA, Hatch JP, Alexander HE. Factors affecting amnesia, seizure duration and efficacy in ECT. Am J Psychiatry 1985;142:692-6.
Nobler MS, Sackeim HA. Augmentation strategies in electroconvulsive therapy: a synthesis. Convulsive Ther 1993;9:331-5 1.
Oliverio A, Castellano C, Puglisi-Allegra S, Renzi P. Diurnal variations in electroconvulsive shock-induced seizures: involvement of endogeneous opoids. Neurosci Lett 1985;57:237-40.
Paylor R, Crawley JN. Inbred strain differences in prepulse inhibition of the mouse startle response. Psychopharmacol 1997;132:169-80.
Posluns DP, Vanderwolf CH. Amnesic and disinhibiting effects of electroconvulsive shock in the rat. J Comp Ph Physiol Psychol 1970;73:291-306.
Pradhan N, Arunasmitha S, Udaya HB. Behavioural and neurochemical differences in an inbred strain of rats. Physiol Behav 1990;47:705-8.
Ramteke S, Andrade C, Faruqi S, Joseph J, Venkataraman BV, Naga Ram MA. BR- 16A attenuates anterograde amnesia induced by electroconvulsive shocks in slow learning rats. Indian J Pharmacology 1995;27:186-8.
Rao SKR. Mental health in Ayurveda. Bangalore: NIMHANS, 1990.
Roullet P, Lassale JM. Radial maze learning using exclusively distant visual cues reveals learners and nonlearners among inbred mouse strains. Physiol Behav 1995;58:1189-95.
Satyavati GV. Leads from Ayurveda on medicinal plants acting on the nervous system. In: Koslow SH, Murthy RS, Coelho GV, eds. Decade of the brain. Rockville, MD: U.S. Department of Health and Human Services, 1995:185-90.
Shaw N. Disruption of conditioned taste aversion: the effect of ECS after the taste-illness interval. Physiol Behav 1986;38:431-4.
Van Buskirk R, McGaugh JL. Retrograde amnesia and brain seizure activity in mice: strain differences. Exp Neural 1973;51:150-9.
Van Ree JM, de Wied D. Behavioral approach to the study of the rat brain. Discussion in Neurosciences 1988;5:1-60.
Vinekar AS, Andrade C, Sriprada VT, George J, Joseph T, Chandra JS. Attenuation of ECS-induced retrograde amnesia by using an herbal formulation. J ECT 1998:14:83-8.
next: Participate In An ECT Evaluation
|