Evaluation of in vitro cytotoxic effect of Trichosanthes dioica root

dioecious Methods: Present study was aimed to evaluate in vitro cytotoxic effect of dichloromethane (DCTD), methanol (METD), and aqueous (AQTD) extracts of T. dioica root using Allium cepa root meristems by keeping them in different concentrations of each test extract under specific experimental conditions followed by determination of root growth inhibition (root length and number) and mitotic index. Results: All the extracts significantly demonstrated concentration-dependent inhibition of root length and number and reduction in mitotic index, indicating antimitotic activity demonstrating cytotoxicity and genotoxicity. DCTD was found to be the most potent (EC 50 : 2.8 mg/ml), followed by METD and AQTD. Conclusion: The present study therefore, establishes promising in vitro cytotoxic and genotoxic property of T. dioica root against the test system.


Evaluation of in vitro cytotoxicity (Allium test)
This study was conducted as per the methods reported by previous workers with requisite modifications. [8,9]

Allium cepa bulbs
Approximately equal size bulbs (40 ± 10 g) of the onions (Allium cepa L.) were obtained from the local Market at Chendernagore, West Bengal. Any onions that were dry, moldy or have started shooting green leaves were discarded.

Growing Allium cepa meristems
The outer scales were removed from the healthy onion bulbs leaving the root primordia intact. These bulbs were grown in dark for 48 h over 100 ml of tap water at ambient temperature until the roots have grown to approximately 3 cm. The water was changed daily during this period. The viable bulbs were then selected and used for subsequent studies.

Exposure to test samples
The bulbs with root tips grown up to 2-3 cm were removed from the water and placed on a layer of tissue paper to remove excess of water. The bulbs were divided into 18 groups (n =12), each six groups for each test extract. The first group for each extract served as control. Immediately, the bulbs were placed in test tubes filled with test samples (one bulb in each) and control (tap water) and incubated at 22 ± 2ºC for 96 h away from direct sunlight. The test samples were changed daily with fresh ones. The length of roots grown during incubation (newly appearing roots not included), root number and the mitotic index were recorded after 96 h. After this period the root appearance was also noted. The effective concentration for 50% root length inhibition (EC 50 ) was determined by plotting treatment concentration against root length as percentage of control.

Microscopic studies and determination of mitotic index
After 96 h, the root tips (2-3 mm) were collected and prepared for microscopic studies by standard aceto-orcin squash preparation technique. [10] For each root tip, the numbers of mitotic cells and total meristematic cells were counted in 5-8 fields of view using high resolution (100×) bright field light microscopy. Mitotic index was represented in terms of dividing cells/total cells and expressed as percentage.

Statistical analysis
The data are presented as the mean ± Standard Error of Mean (SEM). The data were analyzed for statistical significance by Student's 't' test. P values less than 0.05 (p ≤ 0.05) were considered as statistically significant.

RESULTS
The results for cytotoxic effects of different extracts from T. dioica root are summarized in Tables 1-3. All the test extracts exhibited significant (P < 0.001) inhibitory effects on root growth (root length and number) and reduction

DISCUSSION
In the present investigation, the in vitro cytotoxic effects of defatted DCM, MeOH and aqueous extracts of T. dioica were evaluated by using Allium cepa root meristem model (Allium test), where root growth inhibition and antimitotic effects provided the indication of cytotoxicty. Allium test is a rapid, highly sensitive and reproducible bioassay for detecting cytotoxicity and genotoxicity; and shows good agreement with results obtained from other test systems. [9,11] Here, cytotoxicity of all test extracts were evidenced by evaluating macroscopic parameters, i.e., reduction in root number and the most importantly, root length, both of which were indicative of root growth inhibition. The cytotoxic effect was further confirmed by microscopic studies involving determination of mitotic indices reduction of which allowed assessment of impaired cell division (antimitotic effect) thereby providing definitive information regarding the extent of cytotoxic action. Both growth inhibition and antimitotic effects were found to be in concert, as growth inhibition had been the inevitable consequence of diminished cell division.
DCTD exhibited maximum and remarkable cytotoxic potential followed by METD and AQTD. The EC 50 values (calculated on the basis of root length inhibition) of DCTD and METD were 2.8 and 122 mg/ml respectively, while that of AQTD was not found. Thus AQTD could be potentially less cytotoxic while still inhibiting cell divisions at higher concentrations. There were irreversible changes in root tip cells resulting in their growth retardation and cessation. The change in color of DCTD treated roots to brownish was due to cytotoxic effects causing cell death. [11] Preliminary phytochemical analysis revealed the presence of various compounds in METD, whereas the DCTD mainly contained triterpenoids and steroids. It appears that the presence of triterpenoids and/or steroids was responsible for the enhanced activity of DCTD. In this connection, it is noteworthy to mention here that METD also contained triterpenoids and steroids, along with several other constituents, but the expected synergistic effect, however, was not observed here, as DCTD was more active than METD. AQTD exhibited the weakest effect, possibly because of the absence of triterpenoids and steroids. Some synergy was obvious, indicating METD to be more active than AQTD, because of the presence of triterpenoids and steroids in METD. Nevertheless, activity in AQTD indicated that not only triterpenoids and steroids were responsible for the cytotoxic activity. Dereplication strategies based on these findings could be helpful for isolation of the active cytotoxic constituents.
With respect to these results it is apparent that T. dioica root contains cytotoxic constituents that can stop cell division. These constituents plausibly affected the cytoskeleton or inhibited the activity of one or more components of the cell cycle.
The present study confirms the in vitro cytotoxic effect of T. dioica root extracts in Allium test. The results indicate that the METD and DCTD especially, possess potential cytotoxic activity including marked antimitotic effect, but more positive results are definitely needed in other test systems involving in vitro and in vivo animal and human cancer cell lines for qualifying prospective anticancer activity. The present preliminary investigation provides comprehensive in vitro evidence that T. dioica root demonstrates remarkable cytotoxic and genotoxic properties thus suggesting the feasibility of its possible use as natural antitumor agent. Further antitumor studies on T. dioica root using animal cancer call lines are presently underway. 16.2 ± 0.20* 20.1 ± 0.10* 41.1 ± 0.31* Data are expressed as mean ± SEM (n = 12); ¶ P < 0.05 and *P < 0.001 compared to control.