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Einstein (São Paulo)

versão impressa ISSN 1679-4508

Einstein (São Paulo) vol.11 no.2 São Paulo abr./jun. 2013

https://doi.org/10.1590/S1679-45082013000200005 

ORIGINAL ARTICLE

 

Effects of Panax ginseng, Turnera diffusa and Heteropterys tomentosa extracts on hippocampal apoptosis of aged rats

 

 

Andréia Gomes BezerraI; Soraya Soubhi SmailiI; Guiomar Silva LopesI; Elisaldo Araújo CarliniI

IUniversidade Federal de São Paulo, São Paulo, SP, Brazil

Correspondence

 

 


ABSTRACT

OBJECTIVE: To verify if the medicinal plants Panax ginseng C.A. Mey, Turnera diffusa Willd. ex Schult., and Heteropterys tomentosa O. Mach., which are amply used by the population as tonics and cognition enhancers, could have a protective effect on cell death by apoptosis, since this could be one of the mechanisms of action of these substances.
METHODS: Aged male Wistar rats (n=24) were divided into four groups. Over 30 days, three groups received treatments with hydroalcoholic extracts of the plants, and one group received saline solution. A fifth group with young adult male Wistar rats (n=4) received saline solution during the same period. Using the TUNEL technique, the percentage of apoptosis in the hippocampus of these animals was evaluated.
RESULTS: No differences were observed between the percentage of apoptotic cells in the hippocampus of aged animals and of young control animals. The percentage of apoptosis in the hippocampus of aged animals treated chronically with the extracts from the three plants also did not differ from the percentage of apoptosis in the hippocampus of the control group of aged animals.
CONCLUSION: Treatment with the hydroalcoholic extracts of Panax ginseng, Turnera diffusa, and Heteropterys tomentosa did not influence the apoptosis of the hippocampal cells of aged rats.

Keywords: Plants, medicinal; Apoptosis; Aging; Hippocampus


 

 

INTRODUCTION

The process of aging causes a series of physiological and anatomical alterations(1). Among these changes, the gradual loss of various cognitive functions is worth mentioning, including attention, reasoning, orientation, language, and especially memory(2). In this case, the hippocampus, a brain structure intimately related to memory, would be particularly compromised(3).

It is known that neuronal loss is a process that does not occur on a large scale or homogeneously in all areas of the brain, but it is suggested that it is involved in cognitive decline resulting from aging(4). Among the biological mechanisms of neuronal loss, apoptosis stands out and can be related to diverse pathogenic processes. An excess in apoptosis rates is related to cellular degeneration caused by oxidative stress(5,6), frequently associated with aging(7,8). Apoptosis is also related to pathogenesis of neurodegenerative conditions, such as Alzheimer's disease(9), Huntington's disease(10) or Parkinsonism(11). Apoptosis may also be involved in the deficit of memory and in hippocampal function(12).

The plants studied in this paper, Panax ginseng, Turnera diffusa (popularly known as "damiana"), and Heteropterys tomentosa (popularly known as "nó-de-cachorro", in Portuguese), have widespread use that coincides with a possible nootropic or adaptogenic action. Nootropic are drugs characterized by improvement of a person's cognitive performance, and do not possess a specific chemical class or mechanism of action(13). Adaptogenic substances, on the other hand, promote increased physical performance or resistance to stress(14).

Panax ginseng was chosen since there are several studies in literature that confirm its adaptogenic action and show positive effects on memory, evaluated by means of improved performance of rats submitted to avoidance testing(15). It was also observed that ginseng extract has a protective effect on death by apoptosis in SK-N-MC neuron cells(16) and astrocytes(17).

A bibliographic survey points out that Turnera diffusa and Heteropterys tomentosa have uses that fit in with the adaptogenic concept and are among those most often used by the Brazilian population(18), but there are not many scientific studies confirming these beneficial effects. Turnera diffusa is described as a stimulant, tonic, and aphrodisiac agent(19). The possible aphrodisiac action, its primary popular reason for usage, was assessed in a pharmacological investigation(20). In this study, hydroalcoholic fluid extracts of Turnera diffusa and Pfaffia paniculata improved the copulatory performance of sexually incapacitated rats. In a passive avoidance test, a standardized extract of Heteropterys tomentosa was effective in reversing the memory deficit in aged animals(21). The plant also showed a good antioxidant index over lipoperoxidation in vitro(22).

 

OBJECTIVE

Considering cognitive decline resulting from aging, the importance of the hippocampus for this process and the potential neuroprotective effect of the plants under consideration, this study aimed to evaluate the effects of hydroalcoholic extracts (HE) of the roots of Panax ginseng, of the aerial portions of Turnera diffusa, and of the roots of Heteropterys tomentosa on the apoptosis rate of hippocampal cells in aged rats.

 

METHODS

Botanical material

Aerial parts of Turnera diffusa were obtained commercially, from Quimer Ltda. (batch 011, valid until November, 2006), while the roots of Panax ginseng (batch GINP04/02, valid until June, 2008) and Heteropterys tomentosa (batch NOC06/02, valid until August, 2008), in powder form, were obtained commercially from Santos Flora®, all of them provided with official proof of botanical identification of the species. The HEs were prepared by the turbolysis technique(23). Posteriorly, they were freeze-dried (freeze dryer EDWARDS Pirani 501) to obtain dry extracts, which were stored inside a desiccator in the refrigerator.

Animals

Twenty-four male Wistar aged rats were used (20 month-old) along with four young adult rats (3 month-old), provided by the experimental animal facility – Department of Psychobiology of the Universidade Federal de São Paulo (UNIFESP). All animals were maintained in rooms with controlled temperature (23±2°C) and a 12-hour light/dark cycle, with water and food ad libitum. The animals were euthanized by decapitation. The project was submitted to and approved by the Ethics Committee of UNIFESP (protocol number 0464/05).

Treatment of the animals

The aged rats were divided into four groups and received the treatments orally for 30 days. The groups received 100mg/kg of Panax ginseng extract, a dosage effective in learning and memory of rats(15), 50mg/kg of Heteropterys tomentosa, a dosage that reversed the memory impairment of aged rats(21), and 500mg/kg of Turnera diffusa. Both control groups (aged control group and young control group) received saline solution orally for 30 days.

On the 30th day of treatment, one hour after administration, the animals were anesthetized with ketamine (0.8mL/kg) and xylazine (0.5mL/kg) and submitted to transcardiac perfusion with 4% formaldehyde solution. Next, the animals were decapitated, and the brains were carefully removed and stored in 4% formaldehyde for 48 hours for further paraffin inclusion.

Analysis of apoptosis by the TUNEL (TdT-mediated dUTP-biotin nick end-labeling) immunohistochemical method

To use the TUNEL method, a kit was acquired (ApopTag Plus-peroxidase from ONCOR, Inc., USA), following the manufacturer's protocol and the description by Lopes et al.(8).

The animal brains included in paraffin were sliced with a microtome. Tissue sections were deparaffinized with 95 to 70% ethanol and washed in PBS. After the immunohistochemical reaction sequence, the color of positive cells was revealed with the use of diaminobenzidine (DAB) and the use of Carrazi hematoxylin for counterstaining.

The slides were observed under a light microscope. The percentage of positive cells was calculated for the TUNEL reaction in the hippocampus regions (CA1, CA3, and dorsal and ventral dentate gyri). The percentage was obtained by counting the number of cells marked by the reaction relative to the total number of cells present in the granular layers of the said regions [(apoptotic cells/total number of cells) X 100].

Statistical analysis

For data analysis, one-way ANOVA was used. The results were expressed as mean±standard error of the mean (SEM) and a 5% significance level was adopted (p<0.05).

 

RESULTS

On table 1, we observe that the percentage of death in the hippocampal regions analyzed by the TUNEL reaction showed no statistically significant differences between the groups of aged and young animals. Additionally, the aged rats treated with the three different plant extracts did not differ from the animals with no treatment.

 

 

DISCUSSION

This present study aimed to assess the possible anti-apoptotic effect of three HEs (Panax ginseng, Turnera diffusa, and Heteropterys tomentosa) during aging. The animals were treated for 30 days with the plant HEs under study. The brains of these animals were removed for posterior TUNEL reaction. Regions CA1, CA3, and dorsal and ventral dentate gyri of the hippocampus were analyzed as to percentage of neuron death. The regions analyzed by the TUNEL reaction showed no statistically significant differences among the groups of aged animals treated with the three different plant extracts.

There are various studies of vegetable-origin substances aiming at an anti-apoptotic effect on the central nervous system cells(24-26). Methanolic extracts of Acori graminei and Uncariae ramulus et uncus protected the hippocampus from cellular death induced by ischemia(24). A Chinese medicine preparation called Toki-shakuyaku-san showed a neuroprotective effect against the beta-amyloid protein, an effect attributed to its antioxidant action(26). The injection of Carthamus tinctorius extract in rats decreased the area of cerebral infarct and the expression of caspase-3 (a pro-apoptotic protein)(25). These studies prove that extracts from vegetable species can show a protective effect against neuron death in various animal models. However, despite the plausibility of the statement above, in the present study, no protection was noted against neuron death by apoptosis.

Additionally, in this study, there were no differences between the percentages of apoptotic cells in the group of aged animals and the group of young animals, both without treatment. This fact raises questions as to the statement that aging and neuron loss are concomitant events. In fact, neuron loss in aging is discussed by many authors. Part of them has demonstrated that aging is associated with a physiological decrease in the total number of cells in some regions of the brain. In this sense, Ishimaru et al.(27) observed that the number of cells in the hippocampus of aged rats is 10 to 30% lower than in young rats. An increase in apoptosis was found in the striate of adult and aged rats by means of the TUNEL reaction, which could be related to this cellular decrease in the central nervous system(28). However, other studies suggested that this neuron loss during aging is smaller than in newborns, when comparing the brains of newborn rats with those of adult and aged rats(29). These authors noted that in the neocortex, brainstem, hippocampus, and cerebellum, there was a smaller number of apoptotic cells in aged than in newborn animals. In the newborns, this high rate of apoptosis is intimately connected with development, proliferation, and cellular migration(29). Other authors also analyzed the bulb, cerebellum, and corpus callosum in aged animals(30).Thus, the relation between aging and apoptosis is still not totally defined.

The data of the present study are in accordance with some findings in literature that describe the absence of a large number of apoptotic cells in the brain of aged animals. The results of the present study also suggest that the medicinal plants evaluated do not have an anti-apoptotic effect on the central nervous system. Nevertheless, for the correct interpretation of the data, some methodological reservations and limitations must be considered. First, given that there were no high apoptosis rates in the aged animals, any anti-apoptotic effects of the plants analyzed could have been concealed. In this respect, in future studies it would be useful to use methods of induction of apoptosis and neuron death. Furthermore, only neuron death by apoptosis was addressed, omitting mechanisms such as necrosis and autophagy. In this way, one cannot conclude that these plants do not possess a protective effect against neuron death in general. Finally, one should consider that apoptosis induced by aging is not restricted to the hippocampus. Thus, studies that investigate the effects of the plants analyzed on other brain structures may be of great worth.

It is important to remember that the plants studied are commonly used by the general population that recognizes its effects as adaptogens or nootropics. Scientific studies with vegetable substances that display neuroprotection and anti-apoptotic effects are scarce when compared to the quantity of plants described with this finality, whether popular or with scientific literature data. In this respect, it is important to deepen these studies in order to clarify the mechanism of action of these plants, so widely used by the population.

 

CONCLUSION

The extracts of Panax ginseng, Turnera diffusa, and Heteropterys tomentosa do not display any effect on apoptosis rates of the hippocampus of aged rats. These results are specific for the experimental conditions used, and it is necessary to evaluate the effect of these plants by means of studies that induce apoptosis or that assess cognitive decline typical of aging by means of other neurobiological mechanisms.

 

ACKNOWLEDGEMENTS

The authors wish to thank Luciane de Souza for technical assistance given and the Associação Fundo de Incentivo à Pesquisa (AFIP), the coordination for the Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES), and the Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) for the financial aid.

 

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Corresponding author:
Andréia Gomes Bezerra – Rua Botucatu, 862 – Vila Clementino
Zip code: 04023-006 – São Paulo, SP, Brazil
Phone: (55 11) 2149-0155
E-mail: andreia.bzr@gmail.com

Received on: Sep 7, 2012
Accepted on: Apr 2, 2013
Conflict of interest: none.

 

 

Study carried out at Universidade Federal de São Paulo, São Paulo, SP, Brazil.

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