Pharmacognosy Magazine

ORIGINAL ARTICLE
Year
: 2012  |  Volume : 8  |  Issue : 30  |  Page : 129--134

Biodistribution properties of cleistanthin A and cleistanthin B using magnetic resonance imaging in a normal and tumoric animal model


Subramani Parasuraman1, Ramasamy Raveendran1, Mehdi Shafiee Ardestani2, Ramesh Ananthakrishnan3, Ali Jabbari-Arabzadeh2, Mohammad Shafiee Alavidjeh2, Mohammad Reza Aghasadeghi2, Sundararajan Elangovan3, Halanaik Dhanapathi4,  
1 Department of Pharmacology, Jawaharlal Institute of Postgraduate Medical Education and Research, Pondicherry, India
2 Department of Nanobiotechnology and Hepatitis B/AIDs, Pasteur Institute of Iran, Tehran, Iran
3 Department of Radiodiagnosis, Jawaharlal Institute of Postgraduate Medical Education and Research, Pondicherry, India
4 Department of Nuclear Medicine, Jawaharlal Institute of Postgraduate Medical Education and Research, Pondicherry, India

Correspondence Address:
Subramani Parasuraman
Department of Pharmacology, Jawaharlal Institute of Postgraduate Medical Education and Research, Pondicherry
India

Abstract

Aim: To determine the biodistribution properties of cleistanthin A and cleistanthin B in rodents using magnetic resonance imaging (MRI). Materials and Methods: Cleistanthins A and B, constituents of Cleistanthus collinus Roxb., were labelled with gadolinium (Gd 3+ ) directly and injected into normal and tumoric nude mice. The tissue signal intensity was measured using MRI to perform a noninvasive kinetic assay. Wistar rats were used for determination of the grayscale intensity to observe the distribution patterns of of cleistanthins A and B. Results: Cleistanthin A is kinetically more attractive to the gastrointestinal tract than is cleistanthin B, which gets accumulated in muscular tissues of mice in greater concentrations compared with cleistanthin A. Cleistanthin B but not cleistanthin A showed tumoric affinity and exhibited a tumor kinetic attraction in tumoric mice. In rats, cleistanthin A showed greater grayscale intensities in the brain, liver, and skeletal muscles in immediate post contrast MRI images, whereas the gadolinium tagged cleistanthin B showed higher grayscale intensities in the cardiac muscle and skeletal muscles in delayed post contrast MRI images. Conclusions: Cleistanthin A is more pharmacokinetically attractive to the gastrointestinal tract than cleistanthin B.



How to cite this article:
Parasuraman S, Raveendran R, Ardestani MS, Ananthakrishnan R, Jabbari-Arabzadeh A, Alavidjeh MS, Aghasadeghi MR, Elangovan S, Dhanapathi H. Biodistribution properties of cleistanthin A and cleistanthin B using magnetic resonance imaging in a normal and tumoric animal model.Phcog Mag 2012;8:129-134


How to cite this URL:
Parasuraman S, Raveendran R, Ardestani MS, Ananthakrishnan R, Jabbari-Arabzadeh A, Alavidjeh MS, Aghasadeghi MR, Elangovan S, Dhanapathi H. Biodistribution properties of cleistanthin A and cleistanthin B using magnetic resonance imaging in a normal and tumoric animal model. Phcog Mag [serial online] 2012 [cited 2021 May 7 ];8:129-134
Available from: http://www.phcog.com/text.asp?2012/8/30/129/96559


Full Text

 Introduction



Cleistanthin A and cleistanthin B are two of the many constituents of the leaves of Cleistanthus collinus Roxb. (Euphorbiaceae). This plant is commonly used as a suicidal and homicidal poison in Southeast Asian countries, [1] and cleistanthins A and B have been reported to be responsible for toxic effects in human beings. [2],[3] Arylnaphthalide lignin glycosides are the major phytoconstituent of the genus Cleistanthus. They are also present in Phyllanthus taxodiifolius, Haplophyllum buxbaumii, and Cleistanthus patulus. [4] Although cleistanthins A and B have been reported to produce toxicity, the distribution patterns of the compounds and its significance have not been reported. This study was designed to determine the distribution pattern, accumulation sites, tissue binding nature and possible absorption and excretion patterns of cleistanthins A and B in rodents after administering gadolinium (medical diagnostic contrast) tagged compounds and examining them under a magnetic resonance imaging (MRI) system.

 Materials and Methods



This collaborative study was conducted in the departments of Pharmacology, Radiology and Nuclear Medicine, Jawaharlal Institute of Postgraduate Medical Education and Research (JIPMER), Pondicherry, India, and at the Department of Nanobiotechnology and Hepatitis B/AIDS, Pasteur Institute of Iran, Tehran, Iran.

Plant material

Taxonomically identified Cleistanthus collinus Roxb. (Euphorbiaceae) plant parts were collected in Pondicherry and in rural parts of Villupuram and Cuddalore districts of Tamil Nadu, India. They were identified and certified by the Botanical Survey of India (BSI), Coimbatore (reference number BSI/SC/5/23/08-09/Tech. 241). Leaves of Cleistanthus collinus were collected in the months of February-April every year. A voucher specimen of the plant is kept in the Department of Pharmacology, JIPMER, for further reference.

Isolation of cleistanthin A and cleistanthin B

Cleistanthin A and cleistanthin B were isolated from leaves of the Cleistanthus collinus plant. The acetone extract was obtained from defatted powered leaves. This extract was dissolved in benzene and passed through a neutral alumina column and eluted with a benzene and with benzene:ethyl acetate (4:1), benzene:ethyl acetate (1:1), and methanol:chloroform (9.5:0.5) mixtures to isolate fractions of fatty alcohol, collinusin, cleistanthin A, and cleistanthin B, respectively. The fractions of cleistanthin A and cleistanthin B were purified, and the functional groups and facial arrangements of the molecules were confirmed by spectroscopic analysis. [5],[6],[7]

Animals

Nude mice (16-20 g) and Wistar rats (150-180 g) of both sexes were used for the experiment. The nude mice were obtained from the Pasteur Institute of Iran and allowed to adapt to the laboratory conditions for a week. The Wistar rats were obtained from the central animal house of JIPMER, Pondicherry, and allowed to adapt to the laboratory conditions for a week. All the experimental animals were housed at a temperature of 21 ± 2 °C and 60-70% relative humidity in a 12:12 ± 1 h light-dark cycle. The animals were provided with an adequate standard rodent pellet diet and tap water ad libitum. The experimental protocol was approved by the local ethics committee of the Pasteur Institute of Iran, Tehran, Iran and Institute Animal Ethics Committee (IAEC) of JIPMER, Pondicherry, India. All the animal experiments were carried out in accordance with the guidelines of the Committee for the Purpose of Control and Supervision of Experiments on Animals (CPCSEA), India.

Tagging compounds

The direct labelling method was used for tagging cleistanthin A and cleistanthin B with gadolinium (Gd 3+ ). Two millimoles each of cleistanthin A and cleistanthin B were mixed with 2 mmol of meglumine in distilled deionized water. Meglumine (Pubchem CID: 8567) is an amino sugar derived from sorbitol and used to enhance visualization of tissues in medical imaging systems. The pH value of the mixture was adjusted to 7.5, and 5 mmol of vitamin C (antioxidant) was added with constant stirring for 10 min. Then, gadolinium chloride (GdCl 3 , 1 mmol) was added drop by drop into the mixture. The preparation containing cleistanthin A/ cleistanthin B in meglumine, vitamin C, and GdCl 3 was incubated at room temperature with constant stirring for 2 h. The binding efficacy of cleistanthin A and cleistanthin B with GdCl 3 was assessed using thin layer chromatography (TLC) with remade silica gel as the stationary phase and ethanol:sulfuric acid (9.5:0.5) as the mobile phase. [8],[9]

Confirmation of complex formation

Size-exclusive HPLC (SE-HPLC) was employed for analysis of the complex formed by cleistanthins A and B with gadolinium. The electrochemical detection (ECD) system consisted of a Shimadzu SCL 10-Avp system controller, LC-10AS pump, SIL-10A cooled autoinjector, CT0-10A oven, LECD-6A electrochemical detector, and Gastorr online degasser (ISS, England). Class VP-5 software (Shimadzu) was used with the system. All samples were injected into a reverse phase Luna 5 μm C 18 250 mm × 4.6 mm column (Phenomenex), which was protected by Krudkatcher disposable pre-column filters (Phenomenex) and Security Guard cartridges (Phenomenex).

A mixture of 0.1 M disodium hydrogen orthophosphate and 50 μM EDTA (pH 5.6, 1 M OPA) and HPLC grade methanol (35:65) was used as the mobile phase. This mobile phase was filtered through Millipore 0.45 μm HV Durapore membrane filters (AGB, Dublin) and vacuum degassed prior to use. Compounds were eluted isocratically over a 20 min runtime at a flow rate of 0.65 ml/min after a 20 μl injection. The column was maintained at a temperature of 30 °C, and samples/standards were maintained at 4 °C in the autoinjector prior to analysis unless otherwise stated. The glassy carbon working electrode, combined with an Ag/AgCl reference electrode (Shimadzu), was operated at +0.8 V unless otherwise specified, and the range of the detector was set to 1.

Quantitative data analysis

T1- and T2-weighted SE images at 1.5 T (TR/TE = 250 ms/16 ms and TR/TE = 4000 ms/64 ms) were analysed qualitatively. The signal intensities of vials with contrast medium in solution and contrast medium in cells with corresponding iron concentrations were visually compared.

The magnetic resonance (MR) images were transferred as DICOM (Digital Imaging and Communications in Medicine) images to DICOM Works software (Phillipe Puech and Loic Boussel. v 1.3.5). For each concentration, triplicate sampling and the maximum region of interest were considered.

All imaging protocols were done on a 1.5 T GE MRI (Sigma) system. The relaxation rates of gadolinium-loaded-complex contrast agents were measured for different concentrations of the gadolinium-loaded-complex samples, using different spin echo (SE) and gradient echo (GE) protocols. For T2 measurement, two multi-echo SE protocols were used with echo time (TE) values of 12, 24, 36, and 48 ms and 46, 92, 138 and 184 ms, respectively (repetition time [TR] =1000 ms) (Equation 1).

[INLINE:1]

TR-variable SE imaging (with the same TE values) was used for T1 measurement. For T2 measurement, multi-echo SE protocols were used with TR values of 60, 140, 240, 340, 440, 600, 800, 1000, 1500, 2000, 3000, and 5000 ms (TE = 11 ms). The signal intensity equation used for T1 measurement was as follows:

[INLINE:2]

T1 and T2 maps were calculated assuming a monoexponential signal decay. T1 maps were calculated from four SE images with a fixed TE of 11 ms at 1.5 T and TR values of 60, 140, 240, 340, 440, 600, 800, 1000, 1500, 2000, 3000, and 5000 ms using a nonlinear function least-square curve fitting on a pixel-by-pixel basis. The signal intensity of each pixel as a function of time was expressed as follows: SIpixel xy(t) = So(pixel xy) [1 − exp (−t/T1pixel xy)]. [10]

T2 maps were calculated accordingly from four SE images with a fixed TR and TE values of 12, 24, 36, and 48 ms. The signal intensity for each pixel as a function of time was expressed as follows: SIpixel xy(t) = So (pixel xy) exp (t/T2pixel xy). Care was taken to analyse only data points with signal intensities significantly above the noise level. The T1 and T2 relaxation times (s) of the samples in the Eppendorf tubes were obtained from ROI measurements of the test samples on these T1 and T2 maps, and the results were converted to R1 and R2 relaxation rates (s−1 ).

Cancer animal model

Nude mice were xenografted in the right foreleg muscle with 4 × l0 6 human non-small-cell lung cancer [NSCLC] cells. Two weeks later, the tumors attained a size of about 4 mm (diameter).

In vivo imaging of cleistanthin A and cleistanthin B

Nude mice (16-20 g) of either sex were used for the study. Each animal was anaesthetized with ketamine (50 mg/kg) and xylazine (5 mg/kg). [11],[12] The tail vein was cannulated, and 20 mg/kg of tagged cleistanthin A/cleistanthin B was injected. The animal was then placed in a clinical MRI apparatus (1.5 T, GE Sigma). T1-weighted MRI procedures were performed prior to and 20 min after injection. The imaging procedures were also performed on tumoric nude mice.

Determination of grayscale intensity

The grayscale intensity is a measure of the intensity of light at each pixel in a single band of the electromagnetic spectrum. A fasted male rat (8-10 h) was anesthetized using ketamine (80 mg/kg, i.p.) and xylazine (16 mg/kg, i.p.). The animal was placed on a surgical platform, and the skin on the right thigh was exposed and disinfected. A small incision was made in the right thigh, the femoral vein was identified, and cannulated with a 26G × 1/2″ needle, and 20 mg/kg of tagged cleistanthin A or cleistanthin B was injected. [11],[12] The animal was placed in a clinical MRI apparatus (1.5 T, Siemens, Germany). A delayed post-contrast image was taken 30 min after i.v. injection of plain gadolinium as Gadobenate Dimeglumine (MultiHance® ). The pre-contrast, immediate, and delayed post-contrast images were taken for all the animals. The grayscale intensities were calculated for all the animals, and the difference in intensity was determined between the pre-contrast and immediate post-contrast images and between the pre-contrast and delayed post-contrast images. The mean ± SD signal intensity values were calculated for a region of interest with an area of 1.0-1.2 sq. cm, comprising around 35-40 pixels.

 Results



The binding efficacies of cleistanthin A and cleistanthin B with gadolinium were 82% and 78%, respectively [Figure 1]. The T1 relaxivity values of cleistanthins A and B at 37°C were 62.5 and 60.3 mM s−1 , respectively. The T2 relaxivity values of cleistanthin A and B at 37°C were 24.4 and 22.1 mM s−1 , respectively. The ratio of R2 to R1 for cleistanthins A and B were 2.56 and 2.88, respectively. It can be seen that cleistanthins A and B caused a decrease in both the relaxation times T1 and T2 compared with Magnevist® and water [Figure 2]. The T1 and T2 relativity values (calculated from Equations (1) and (2)) are shown in [Table 1]. The in vitro studies showed the relaxivity values of cleistanthins A and B to be 62.5 and 60.3 mM -1 s -1 relaxivity for Cleistanthins A and B, respectively.{Table 1}{Figure 1}{Figure 2}

A schematic illustration of the performance of in vitro T1/T2 measurements using an MRI apparatus is shown in [Figure 3]. For each concentration, triplicate sampling and the maximum region of interest were considered. Five concentrations of tagged cleistanthin A and cleistanthin B (0.33, 0.17, 0.08, 0.04, and 0.02 mmol/mL) were obtained by dilution with 0.9% sodium chloride. The in vivo drug distribution patterns in normal and cancer nude mice were obtained 20 min after injection (i.v.) of tagged cleistanthin A or cleistanthin B and are presented in [Figure 4],[Figure 5] and [Figure 6]. The in vivo drug distribution study with 1.5 T MRI showed that (a) cleistanthin A was more pharmacokinetically attractive to the gastrointestinal tract compared with cleistanthin B and that (b) cleistanthin B is being increasingly accumulated in muscular tissues rather than cleistanthin A.{Figure 3}{Figure 4}{Figure 5}{Figure 6}

The difference in grayscale intensity is presented in [Table 2] and [Table 3] and in [Figure 7] and [Figure 8]. While the gadolinium tagged cleistanthin A showed greater grayscale intensities in the brain, liver, and skeletal muscles under immediate MRI, the gadolinium tagged cleistanthin B showed greater grayscale intensities in the cardiac muscle and skeletal muscles under delayed MRI.{Table 2}{Table 3}{Figure 7}{Figure 8}

 Discussion



This study suggests that both cleistanthin A and cleistanthin B get accumulated in the gastrointestinal tract. Compared with cleistanthin B, cleistanthin A was found in greater quantities in the gastrointestinal tract, and this may be due to differences in the physicochemical properties of the compounds. The same could be the reason for cleistanthin B getting accumulated in muscular tissues in larger quantities compared with cleistanthin A. [13] The accumulation of cleistanthin A and cleistanthin B indicates that these compounds can be absorbed through oral administration. Gastric erosions were reported in patients with Cleistanthus collinus poisoning, and this could be due to accumulation of cleistanthin A and cleistanthin B in the stomach wall. Cleistanthins A and B have been reported to have anticancer effects, and the cytotoxic effects of the accumulated cleistanthins A and B could be the reason for the erosions. Computer-aided tools also predicted that cleistanthins A and B could be absorbed through the gastrointestinal tract by passive diffusion, yielding an oral bioavailability of 30-70% and 30%, respectively. [14]

MRI helps demonstrate the behaviours of gastrointestinal, topical, colloidal, and target drug delivery systems.[15] The grayscale intensity calculation suggests that cleistanthin A is distributed immediately after i.v. administration and gets accumulated in the brain, liver, and skeletal muscles. However, cleistanthin B is distributed slowly after i.v. administration and gets accumulated in the cardiac muscle and skeletal muscles. The MRI of rats and mice indicates that both the compounds are excreted through the kidneys. The results suggest that cleistanthin B has a slow systemic distribution ratio, which may be attributed to differences in the physicochemical properties of the compounds.

 Conclusion



This study leads to the conclusion that both cleistanthin A and cleistanthin B are accumulated in the gastrointestinal tract and distributed to the entire body. While cleistanthin A is accumulated in the brain, liver, and skeletal muscles, cleistanthin B is accumulated in the cardiac muscle and skeletal muscles. Cleistanthin A is pharmacokinetically more attractive to the gastrointestinal tract than is cleistanthin B, which is accumulated in muscular tissues in large quantities.

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