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Comfrey or Symphytum officinale (L.) (Boraginaceae) is a very popular plant used for therapeutic purposes. Since the 1980s, its effects have been studied in long-term carcinogenesis studies, in which Comfrey extract is administered at high doses during several months and the neoplastic hepatic lesions are evaluated. However, the literature on this topic is very poor considering the studies performed under short-term carcinogenesis protocols, such as the ‘resistant hepatocyte model’ (RHM). In these studies, it is possible to observe easily the phenomena related to the early phases of tumor development, since pre-neoplastic lesions (PNLs) rise in about 1–2 months of chemical induction. Herein, the effects of chronic oral treatment of rats with 10% Comfrey ethanolic extract were evaluated in a RHM. Wistar rats were sequentially treated with N-nitrosodiethylamine (ip) and 2-acetilaminofluorene (po), and submitted to hepatectomy to induce carcinogenesis promotion. Macroscopic/microscopic quantitative analysis of PNL was performed. Non-parametric statistical tests (Mann–Whitney and χ2) were used, and the level of significance was set at P ≤ 0.05. Comfrey treatment reduced the number of pre-neoplastic macroscopic lesions up to 1 mm (P ≤ 0.05), the percentage of oval cells (P = 0.0001) and mitotic figures (P = 0.007), as well as the number of Proliferating Cell Nuclear Antigen (PCNA) positive cells (P = 0.0001) and acidophilic pre-neoplastic nodules (P = 0.05). On the other hand, the percentage of cells presenting megalocytosis (P = 0.0001) and vacuolar degeneration (P = 0.0001) was increased. Scores of fibrosis, glycogen stores and the number of nucleolus organizing regions were not altered. The study indicated that oral treatment of rats with 10% Comfrey alcoholic extract reduced cell proliferation in this model.
The systematic study of plants normally used for consumption and that are able to modify the carcinogenesis process has greatly developed over recent years (1–6). Comfrey or Symphytum officinale (L.) (Boraginaceae) is a plant of fast growth, whose leaves and roots are used therapeutically since the XVI century, especially to improve wound healing. Since the 1930s it has been used for animal feed, but this use has been prohibited in Australia and New Zealand (5,7).
The toxic effects of Comfrey were described in the early 1980s and, since then, various pyrrolizidine alkaloids, such as lasiocarpine, lycopsamine, intermedine, symlandine, riddelliine and mainly symphytine have been identified (8–13). Chou and Fu (14) have recently determined that metabolic products of pyrrolizidine alkaloids, such as 6,7-dihydro-7-hydroxy-1-hydroxymethyl-5H-pyrrolizine (DHP)-derived DNA adducts, are formed in the liver of female F344 rats and can be related to its toxic effects.
In long-term protocols, it was demonstrated that these active principles were hepatotoxic, mutagenic and carcinogenic (15). Mei and colleagues (16) observed that dietary comfrey resulted in marked changes in liver gene expression, body weight and mutation frequency. Hirono and colleagues (17) demonstrated that pyrrolizidine alkaloids induced hepatocellular adenoma and hemangiosarcoma with lung metastasis. Also, severe venous-occlusive disease was present in the liver, characterized by hepatocyte swelling, formation of membrane blebs, endothelial proliferation and peri-venular hemorrhagic necrosis with deposition of reticulin (18,19). Liver disease was also identified in cases of human chronic intoxication (20,21), although some aspects of human toxicity of Comfrey has been recently revisited (22).
Among several demonstrations of carcinogenic effects of Comfrey, few studies have reported its anti-neoplastic effects (23). Even though, current information about its action in the initial stages of the carcinogenic process—that could be easily evidenced in short-term protocols—is very poor. Also, most studies of short-term hepatic carcinogenesis were performed using isolated active principles (15,24).
Experimental models of liver carcinogenesis represent a simple and frequently used method for studying the genesis and evolution of neoplasms, because of the size and susceptibility of this organ to cancer (25,26). Likewise, these short-term models—hepatectomy with treatment of animals with carcinogenic substances—are fast to perform, and rigid control of experimental conditions can be achieved without lack the in vivo particularities of carcinogenesis (27). The model used in the present work, resistant hepatocyte model (RHM), was first described by Solf and Faber (28). Thus, a single dose of N-nitrosodiethylamine (DEN) and repeated low doses of 2-acetilaminofluorene (AAF), both initiator agents, are administered concomitantly with hepatectomy, which acts as promotion stimulus. In this model, pre-neoplastic lesions (PNLs) can be seen in the liver as early as 5–10 days after hepatectomy. In the contrary, in long-term models, the prolonged treatment with carcinogens without surgery requires much more time to obtain the same lesions.
Herein, this model was used to study the effects of Comfrey extract on the development of early PNLs in liver.
Adult male Wistar rats weighting 200–250 g were used. They were kept in conventional plastic cages (maximum: five rats per cage) maintained in an exclusive room and were exposed to a controlled light cycle (lights on from 6:30 AM to 6:30 PM) and temperature, which was fixed at 22 ± 2°C. Food and drink were offered ad libitum. All animal care and maintenance procedures were performed according to guidelines of BPL (Brazilian GLP).
Ethical procedures were based on the Brazilian law 6638 (May 8, 1979) ‘Normas para Prática Didático-Científica da Vivissecção de Animais’, which is in accordance to the ‘European Convention for the Protection of Vertebrate Animals used for Experimental and Other Scientific Purposes’ (Strasbourg, March 18, 1986). Moribund rats were sacrificed for humane reasons, by deep anesthesia.
One kilogram of Comfrey leaves harvested from FCAV – Campus Jaboticabal (SP - Brazil) during the winter (July, in Brazil) was soaked with 1 l of 93% ethanol and left to stand for 10 days at room temperature (25 ± 3°C). After this period, the mixture was filtered through conventional filter paper and processed by evaporation methods to obtain the ethanolic extract.
The 10% Comfrey extract was administered to all groups, three times a week, in a volume of 0.02 ml/kg−1 body weight, throughout all the experimental period. This extract concentration was chosen to reproduce the popular method of leaf preparation where toxic effects are described (11). Each group (N = 20 at the beginning of the study) received the treatment by gavage, being the control treated with distilled water and the experimental group treated with the distilled water diluted extract.
Deaths are common in RHM and the rats that died during the study were not analyzed. At the end of the study, the number of surviving rats was eight in the control group and nine in the experimental group. The carcinogenesis protocol was as illustrated in the following scheme:
|Day of experiment||Zero||15–17||18||20,22||30|
|Phase of carcino- genesis||Initiation||Initiation||Promotion||Initiation||–|
|Procedure||Inoculation||Inocula- tion||Hepatectomy (30% of the liver mass)||Inocula- tion||Sacrifice|
|Dose||300 mg/kg (intra- peritoneal)||20 mg/kg (gavage)||–||20 mg/kg (gavage)||–|
DEN, N-nitrosodiethylamine (SIGMA, St Louis, USA); diluted in 0.9% NaCl; 2AAF, 2-acetilaminofluorene (SIGMA, St Louis, USA); diluted in corn oil.
This model, including the hepatectomy technique, was adapted from Dagli and colleagues (29). All carcinogenic substances were handled in a chamber with controlled air output. All personnel involved wore appropriate masks provided with filters against powder and volatile substances, security glasses and double gloves. All material used for injections or gavage was discarded in appropriate boxes for hazardous specimens.
One 5 mm thick central slice was harvested from the left lateral lobe of the liver and fixed in Carnoy solution (3 : 1 : 6 chloroform: glacial acetic acid: absolute alcohol) for 4 h (30). This material was processed by routine histological methods and stained with hematoxylin–eosin, Ag–nucleolus organizing regions (NOR), Masson's trichrome and periodic acid Schiff (PAS). The immunohistochemistry procedures were also made from the same paraffin embedded material.
To perform the histometry of cell types and mitotic figures, photomicrographs of 5 pre-determined fields (top, bottom, laterals and center of the fragment) of each liver slice were obtained using a 200× objective. A grid with 200 points printed on transparent film was superimposed on the photographs and the number of points of intersection incident on each structure was recorded. The structures counted were: oval cells (hepatic steam cells), non-megalocytic and megalocytic hepatocytes (including multinucleated hepatocytes), degenerated (vacuolized) cells and mitotic figures (including typical and atypical mitosis).
PNLs were classified as ‘acidophilic’, ‘mixed’ and ‘clear’ patterns (29) and the total PNLs of each type per slice was counted directly from the microscope (Alphaphot, Nikon, Japan). Fibrosis was scored as follows, on the basis of Masson trichrome staining:
SCORE 0: without evidence of fibrosis
SCORE 1: discrete peri-portal fibrosis
SCORE 2: peri-portal and inter-nodular fibrosis
SCORE 3: peri-portal and inter-nodular fibrosis and capsule thickening
The same scoring method was used to quantify glycogen content of liver cells by PAS staining, as follows:
SCORE 0: without granules
SCORE 1: weak and diffuse granulation
SCORE 2: strong and multifocal granulation
SCORE 3: strong and diffuse granulation
Complementary slides were prepared for AgNOR protein identification using a silver staining method and for PCNA labeling by immunohistochemistry. The NORs were counted as described by Zaczek and colleagues (30). The number of NORs present in histological preparations reflects the quantity of active ribosomal genes and thus the proliferating status of tissues. This method is adequate to verify early stages of cell proliferation, including the interphase of the cell cycle, before the formation of mitotic figures.
The Proliferating Cell Nuclear Antigen (PCNA) positive cells counting was performed by submitting the slides to hot high pressure followed by overnight incubation with 1 : 100 anti-PCNA antibody (mouse anti-human, PC-10 clone, DAKO). The LSAB amplification system was also used. The slides were back stained with hematoxylin. Five microscopic fields were randomly chosen and 500 cells were counted for each slide. The PCNA method reveals the ‘S phase cycle’ positive cells, it means, cells in the early stages of duplication. Positive cells presented strongly nuclear reactivity. The numbers of positive and negative cells were recorded.
All the quantification procedures were done in blind.
F-test to compare variances was first performed to verify the Gaussian distribution of the variables, as a result of which non-parametric Mann–Whitney tests (PNL, NOR, fibrosis and glycogen granules counting) and χ2-test (cell counting) were used. The ‘P’ values were fixed at P ≤ 0.05.
PNL counting on the liver surface is represented in Fig. 1. The number of nodules measuring 1 mm in diameter or less was significantly reduced in Comfrey treated rats, compared to control.
The cell type percentages are given in Table 1. The experimental group showed significant increase in the percentage of megalocytic and vacuolized cells and decrease in oval cells, PCNA positive cells and mitosis, compared to control.
The number of NORs per field and the scores for fibrosis and glycogen granulation on liver slides, respectively stained by Masson trichrome and PAS, did not differ between groups. Table 2 shows the number of PNL according to nodule classification. The experimental group presented significant reduction of acidophilic nodules compared to control.
In short, the results showed a clear protective effect of Comfrey extract on the early stages of induced hepatic carcinogenesis.
In this work, the putative effects of Comfrey extract on the initial stages of neoplastic development were tested. Both, macroscopic and microscopic criteria were considered to evaluate its capacity to change proliferation parameters.
Macroscopically, the number of PNLs was reduced by treatment with Comfrey extract, mainly those measuring 1 mm or less. This particular result suggests that Comfrey extract was able to modulate the early stages of PNL development. These macroscopic findings were supported by the microscopic observations. The increase of the percentage of megalocytic and vacuolized liver cells, associated with the decrease of the percentage of oval cells, PCNA—positive cells, mitotic figures and the number of acidophilic nodules, converge to the anti-proliferation hypothesis. Considering the cell phenotype, the pre-neoplastic nodules are classified according to the following aggressiveness indicators: clear (vacuolized/degenerated) cells, mixed (acidophilic and vacuolized cells in the same nodule) cells, acidophilic (intense protein synthesis) cells and basophilic (intense proliferation activity) cells.
It is important to note that oval cells and acidophilic nodules are typical manifestations of early tumor establishment (29). Thus, their reduction also points toward to a qualitative anti-neoplastic property.
Adding to the earlier described findings, the increase of megalocytosis percentage, the decrease of PCNA-positive cells and cells showing mitosis phenotype also suggest anti-mitotic effects. Some authors consider megalocytosis as a ‘frustrated mitosis’, in which the cell prepares to divide but telophase does not occur (31). This phenotype has been described by other authors in liver models, especially those associated with the effects of pyrrolizidine alkaloids (32), also present in Comfrey extracts (14, 33–35). It is known that chronic ingestion of pyrrolizidine alkaloids by cattle leads to peri-portal fibrosis and bile duct proliferation (33), phenomena related to the proliferation of oval cells. Herein, the reduction on the percentage of these cells reinforces the evidence of anti-mitotic effects (36).
This convergence of results is according the previous studies in which the anti-mitotic effects of pyrrolizidine alkaloids are preponderant over the carcinogenic ones in short-term experimental procedures (37).
The negative result of AgNOR counting may be related to the low degree of sensitivity of this test.
Although scores of glycogen cell stores were not modified, vacuolized hepatocytes were more numerous in treated rats, what could be related to some oxidative toxic effects of Comfrey (36). In fact, degenerative hepatocyte lesions induced by this plant have been described previously (18, 19). The study of Comfrey and other herbs largely used as complementary medicine deserves more specific studies, since plant extracts are chemically diverse and may be able to modulate several metabolism steps simultaneously. Nowadays, some gene expression studies are on the focus of scientific interest for better understanding their molecular mechanisms (38).
To delineate a general hypothesis about the putative mechanism of action of Comfrey extract in this model, a resumed framework is presented in the Fig. 2, showing how the mitotic process could be suppressed at several steps, at the same time.
In conclusion, the present findings can contribute to understand a very particular and under explored Comfrey pharmacological activity, since the treatment of rats with its extract seems to protect them from early development of pre-neoplastic liver lesions, by inhibiting cell proliferation and modulating atypical phenotype.
We thank Vilma Felix dos Santos for preparing the slides, Dr Fernando S. Moreno and Dr Maria Lucia Zaidan Dagli for suggestions about the experimental model, Dr Josmar S. Arrais de Matos, UNISA Pro-rector for Research and Dr Godofredo C. Genofre Netto, UNISA Research Director, for support.