|Year : 2019 | Volume
| Issue : 5 | Page : 217-221
Neuropharmacological evaluation of methanolic extract of Costus speciosus Linn. rhizome in Swiss albino mice
Umay Chen1, Md. Saddam Hussain2, Tanoy Mazumder2, SM Naim Uddin3, Sujan Banik2
1 Department of Pharmacy, University of Chittagong, Chittagong-4331; Department of Pharmacy, Noakhali Science and Technology University, Noakhali-3814, Bangladesh
2 Department of Pharmacy, Noakhali Science and Technology University, Noakhali-3814, Bangladesh
3 Department of Pharmacy, University of Chittagong, Chittagong-4331, Bangladesh
|Date of Submission||14-Mar-2019|
|Date of Decision||25-Mar-2019|
|Date of Acceptance||08-May-2019|
|Date of Web Publication||28-May-2019|
Assistant Professor Sujan Banik
Department of Pharmacy, Noakhali Science and Technology University, Noakhali-3814
Source of Support: None, Conflict of Interest: None
Objective: To evaluate the neuropharmacological properties of Costus speciosus (C. speciosus) rhizome using different experimental mouse models.
Methods: The anxiolytic effect was investigated by hole-board test, elevated plus maze and light/dark test, while central nervous system (CNS) depressant effect was evaluated by thiopental sodium-induced sleep test. Finally, antidepressant effect was evaluated by forced swimming test and tail suspension test.
Results: In both elevated plus maze and hole board test, 400 mg/kg C. speciosus showed more significant CNS depressant effect than 1 mg/kg diazepam. Both 200 mg/kg and 400 mg/kg C. speciosus extract produced a significant dose-dependent decrease in onset of sleep. In forced swimming test, C. speciosus rhizome showed a decrease in duration of immobility in a dose-dependent manner. Imipramine (10 mg/kg) and C. speciosus extract at 400 mg/kg dose exhibited a significant reduction in duration of immobility in tail suspension test which provided additional evidence of antidepressant effect of C. speciosus rhizome.
Conclusions: Our study indicates that C. speciosus rhizome possesses CNS depressant, anxiolytic and antidepressant-like activities. Further studies are warranted determine the exact phytoconstituents and mechanism of action responsible for the neuropharmacological effect.
Keywords: Costus speciosus, CNS depressant, Anxiolytic, Antidepressant
|How to cite this article:|
Chen U, Hussain MS, Mazumder T, Naim Uddin S M, Banik S. Neuropharmacological evaluation of methanolic extract of Costus speciosus Linn. rhizome in Swiss albino mice. Asian Pac J Trop Biomed 2019;9:217-21
|How to cite this URL:|
Chen U, Hussain MS, Mazumder T, Naim Uddin S M, Banik S. Neuropharmacological evaluation of methanolic extract of Costus speciosus Linn. rhizome in Swiss albino mice. Asian Pac J Trop Biomed [serial online] 2019 [cited 2022 Jan 28];9:217-21. Available from: https://www.apjtb.org/text.asp?2019/9/5/217/259002
Umay Chen, Md. Saddam Hussain. These authors contributed equally.
| 1. Introduction|| |
Among the stress-related mental issues responsible for different physiological disorders and early death, anxiety and depressive disorders are most common. It has been assumed and confirmed that more than 20% adult populations suffered these mental conditions during their life. According to the WHO report on mental health, over 1.1 billion people worldwide suffering mental disorder, and people with anxiety disorder account for almost 4 percent of the world population. It is assumed that the total incidence of the disease will increase from 12.3% to 15.0% within the year 2020.
Because of the upward push of this alarming anticipation, WHO speculates that depression will become the second place among causes for premature death and disability within 2020. Depression is considered as a burden for every country and is more severe in third world countries where diagnosis and treatment are inadequate and relatively more expensive. This burden has a significant effect on the total economic and health of every country. Because of various pharmacological side effects and resistance to the chronic treatment, approximately two-thirds of depressed or anxious patients are reacting poorly to the currently available treatment. This situation has led researcheres to investigate medicinal plants which can combat anxiety and depression. Medicinal plant researches have been standardized constantly to search the potent new therapeutic products from plant sources for the remedy of neurological diseases using different experimental animal models.
Our study focused on Costus speciosus (C. speciosus), a flowering plant also known as crepe ginger which belongs to the family Costaceae under the order of Zingiberales. C. speciosus is native to Southeast Asia, commonly grown as medicinal and ornamental plants. The rhizomes of C. speciosus are significant sources of saponins, diosgenin and tigogenin. Previous studies reported that methanolic extract of the rhizome revealed the presence of alkaloids, cardiac glycosides, saponins, and sterols,. Five new compounds were reported to isolate from the rhizomes, tetradecyl 13- methylpentadecanoate, tetradecyl 11-methyltridecanoate, 14- oxotricosanoic acid, 14-oxoheptacosanoic acid and 15- oxooctacosanoic acid. The rhizomes are bitter and have antidiabetic, anti-dyslipidemic, hepatoprotective, antibacterial, antifertility, anti-inflammatory, antipyretic, anti-asthmatic, antifungal and estrogenic activities[13-17]. According to the literature survey, there is no evidence of neuropharmacological effects of methanolic extract of C. speciosus rhizomes. Therefore, this study was performed in order to explore the neuropharmacological potentiality of C. speciosus rhizome.
| 2. Materials and methods|| |
2.1. Collection and identification of plant parts
The rhizome of C. speciosus was collected from Maheshkhali, Bangladesh. Identification and authentication of this plant part were confirmed by National Herbarium of Bangladesh (Authentication number: 43651).
2.2. Drying, grinding and extraction of rhizome of C. speciosus
The collected rhizomes were separated from unwanted materials, flowers and other plant parts. After grind, coarse powders of this plant were dried by a consecutive air drying process without any direct exposure to sunlight. Then, 500 g of ground fine powders was emerged in 1.5 L methanol in a suitable jar and sealed properly for 15 d, while occasional shaking and stirring was employed to agitate the mixture for proper extraction. The filtrate (methanol extract) was obtained after filtration by a piece of smooth, white cotton material, then by Whatman filter paper and finally evaporation by spontaneous natural vaporization method. At the end, 30.2 g of gummy concentrate slight golden color extract was obtained.
2.3. Experimental animals
Swiss-albino mice were used for this study. They were collected from the animal house of Jahangirnagar University, Savar, Dhaka and kept at 20-25 °C and (55±10)% relative humidity. All experimental animals were fed by ICDDRB formulated rodent food and water ad libitum. They were allowed to acclimatize to the laboratory conditions at the least three to four days earlier the date conducting the experiment. All authors hereby declare that “Principles of laboratory animal care” (NIH publication No. 85-23, revised 1985) were followed, as well as specific national laws where applicable. All experiments have been examined and approved by the ethical committee of Noakhali Science and Technology University (Approval no. R-2018070045).
2.4. Study design
Swiss albino mice were randomized into four groups (with five mice in every group). Group-1: Distilled water 10 mL/kg orally, Group-2: Diazepam 1 mg/kg orally in case of anxiolytic test; Diazepam 2 mg/kg orally in case of thiopental induced sleep test; Imipramine 10 mg/kg in case of antidepressant test, Group-3: C. speciosus rhizomes dissolved in distilled water with few drops of Tween 80, 200 mg/kg orally, Group-4: C. speciosus rhizomes dissolved in distilled water with few drops of Tween 80, 400 mg/kg orally.
2.5. Anxiolytic evaluation
2.5.1. Elevated plus maze test
This anxiolytic test was done with the reference of method described by Lister, here an entry was defined as having all 4 paws inside the arm.
2.5.2. Hole board test
Hole board test is an experimental model used for screening anxiolytic activity based on number of head dips in holes. This test was performed with the reference of method described by by File and Wardill.
2.5.3. Light dark test
The light/dark test was performed according to the Bourin and Hascoët method, where rodents were subjected to brightly illuminated regions and their exploratory behaviour in response to slight stressors with subsequent innate aversion was observed.
2.6. CNS depressant evaluation
Thiopental induced sleep test was performed according to the previously defined method. The time to lose righting reflex, without delay after thiopental sodium injection (latent period) and the length of sleep (time between the loss and recuperation of reflex) were observed.
2.7. Antidepressant evaluation
2.7.1. Tail suspension test
Tail suspension test was employed to measure stress in mice. It is primarily based on the theory that if a mouse is subjected to inescapable stress, it would become motionless, which represents the state of depressive nature. Steru et al. described this method for the very first time, on which this experiment was performed.
2.7.2. Forced swimming test
Forced swimming test is another behavioral test to evaluate antidepressant activity and this study used the method described by Porsolt et al.
2.8. Statistical analysis
All the experimental data were analyzed statistically by SPSS version 19 and expressed as mean ± SEM. One-way analysis of variance (ANOVA) followed by Dunnett’s t-test were used for analysis, and P<0.05 was considered to be statistically significant.
| 3. Results|| |
3.1. Anxiolytic evaluation
3.1.1. Elevated plus maze test
Methanolic extract of C. speciosus produced anxiolytic-like effect at both doses level of 200 and 400 mg/kg respectively, which was confirmed by increased time in open arm circumstances and reduced time compared to the control subjects [Table 1].
|Table 1: Effect of C. speciosus rhizome on elevated plus maze test in mice.|
Click here to view
3.1.2. Hole board test
The methanolic extract of C. speciosus increased the number of head dips significantly (P<0.01) at two doses level of 200 and 400 mg/kg (33.6 ± 3.69 and 57.4 ± 2.23, respectively) compared with control group (12.80 ± 1.68), and 400 mg/kg showed more significant result even compared to standard drug group (34.20 ±2.01).
3.1.3. Light dark test
The methanolic extract of C. speciosus increased the time spent in light compartment significantly (P<0.01) at 200 and 400 mg/kg compared with control group [Table 2].
|Table 2: Effect of methanolic extract of C. speciosus rhizome on light dark test.|
Click here to view
3.2. CNS depressant evaluation
Both 200 mg/kg and 400 mg/kg doses of the extract induced a significant decrease in onset of sleep and significantly increased the duration of sleep compared with control group [Table 3]. Extract at 400 mg/kg showed more significant effect than 200 mg/kg.
|Table 3: Effect of methanolic extract of C. speciosus rhizome on thiopental- induced sleeping time test.|
Click here to view
3.3. Antidepressant evaluation
Tail suspension test and forced swimming test all showed that methanolic extract of C. speciosus at two doses and imipramine significantly decreased immobility time compared with control groups (P<0.05) [Table 4].
|Table 4: Effect of methanolic extract of C. speciosus rhizome on tail suspension test and forced swimming test in mice.|
Click here to view
| 4. Discussion|| |
Anxiety and depressive disorders are pathological conditions with high prevalence and play a remarkable role in global morbidity and mortality,. The present study successfully validates the neuropharmacological effects of methanol extract of C. speciosus rhizome.
Elevated plus maze model is a broadly used in vivo method for screening anxiolytic potentiality, in which experimental animals avoiding uncovered open areas of the maze and having a desire for sections enclosed by protecting wall are presumed to be aversive. If tested animals treated with plant extracts showed any statistically significant changes in open arms, it is considered as the sign of anxiolytic effectiveness of this particular plant extract. In this experiment, methanolic extract of C. speciosus produced anxiolytic-like effect at both doses level of 200 and 400 mg/kg, which was confirmed with the increased time spent in open arm circumstances and the reduced time spent in the closed arms.
The anxiolytic effect of C. speciosus is just like diazepam which is a popular drug of benzodiazepine group. The effect of anxiolytic agent is associated with facilitating the opening of the Gamma amino butyric acid (GABA)A-activated chloride channels. Therefore, it can be hypothesized that C. speciosus could act by inducing a benzodiazepine-like substance. Other ways to test anxiolytic effect are hole board test and light dark test. The hole board model is based on the head-dipping behavior of test animals which are sensitive to changes in the emotional state and have increase in head-dipping behavior in anxiolytic-like state,. Crude methanolic extract of C. speciosus at doses of 200 mg/kg and 400 mg/kg showed a significant increase in the number of head dips (33.6 and 57.4, respectively) when compared to the control group (12.8). According to Barua et al, in light/dark test, rodents are subjected to brightly illuminated regions and their exploratory behaviour in response to slight stressors with subsequent innate aversion is observed. This test is useful to determine anxiolytic-like or anxiogenic-like activity of mice. Transition is regarded as an index of activity-exploration because of habituation over time, and the time spent in every compartment is regarded a reflection of aversion. Different classical models are used for different neuropharmacological tests, namely forced swimming, tail suspension, and thiopental-induced sleep tests. GABA is the foremost inhibitory neurotransmitter in the CNS. Involvement of GABA in various neurological disorders such as epilepsy, depression, Parkinson syndrome, and Alzheimer’s disease has been explored. Diverse drugs utilized in various neurological and psychological problems may modify the GABAergic actions, which is acted by increasing synthesis of GABA through potentiating the GABA-mediated postsynaptic inhibition via allosteric changes in GABA receptors. It at once increases the chloride conductance or indirectly potentiates GABA-triggered chloride conductance with simultaneous depression of voltage activated Ca2+ channel like barbiturates,. Therefore, it is presumed that the plant extract may act by potentiating GABAergic inhibition via membrane hyper polarization which leads to a decrease in the firing rate of critical neurons in the brain. Thus an increase in the duration of the GABA-gated ion channel opening and enhanced affinity for GABA may also be responsible for CNS depressant effect.
Thiopental sodium belonging to barbiturate group induces sleep in both human and rodents. Thiopental sodium-induced sleep test is used to investigate sedative-hypnotic drugs. By binding with GABA receptor complex, it exerts GABA mediated hyperpolarization of postsynaptic neurons. All doses of the crude methanolic extracts (200 mg/kg and 400 mg/kg) produced a significant decrease in onset of sleep and increase in duration of sleep when compared to the control group.
For assessment of antidepressant-like effect, the forced swimming test is widely used. In this model, shorter immobility time indicates antidepressant-like activity while extended immobility time indicates CNS depressant-like effect. In forced swimming test, crude methanolic extract of C. speciosus rhizome produced a significant reduction in duration of immobility. Standard imipramine (10 mg/kg) and C. speciosus methanolic extract of 400 mg/kg showed a significant reduction in duration of immobility which confirmed antidepressant-like effect. In tail suspension test, the time of immobility is indicative of a behavioral despair which reflects a depressive state. Crude methanolic extracts at two doses of 400 and 200 mg/kg were found to have significantly reduced immobility time compared to the control group. These results support that the crude methanolic extract of C. speciosus rhizome could possess antidepressant-like effect.
The results of our study demonstrate that methanolic extract of C. speciosus rhizome produces remarkable neuropharmacological effects on experimental mice models. Further investigation is recommended to determine the responsible phytoconstituents and the exact biomedical pathway.
Conflict of interest statement
The authors declare they have no competing interests.
| References|| |
Dang H, Chen Y, Liu X, Pan A, Peng B, Wang Q, et al. Preventive action of Kai Xin San aqueous extract on depressive-like symptoms and cognition deficit induced by chronic mild stress. Exp Biol Med
2009; 234(7): 785-793.
. The world health report 2017 - Mental Health Atlas. Geneva: WHO; 2017
Reynolds EH. Brain and mind: A challenge for WHO. Lancet
2003; 361: 1924-1925.
Patel V, Araya R, Bolton P. Editorial: Treating depression in the developing world. Trop Med Int Heal
2004; 9(5): 539-541.
Ohayon MM. Epidemiology of depression and its treatment in the general population. J Psychiatr Res
2007; 41(3-4): 207-213.
Onasanwo SA, Chatterjee M, Palit G. Antidepressant and anxiolytic potentials of dichloromethane fraction from Hedranthera barteri. African J Biomed Res
2010; 13(1): 76-81.
Panesar G, Kumar A, Sharma A. In vivo
antianxiety and antidepressant activity of Hibiscus sabdariffa
calyx extracts. J Pharm Res Res
2017; 11(8): 962-966.
Zhang ZJ. Therapeutic effects of herbal extracts and constituents in animal models of psychiatric disorders. Life Sci
2004; 75(14): 1659-1699.
Swati S, Agarwal P. Kebuka (Costus speciosus):
A critical review. World J Pharm Pharm Sci
2015; 4(10): 421-429.
Rani SA, Sulakshana G, Patnaik S. Costus speciosus
, an antidiabetic plant- review. J Pharm Res
2012; 1(3): 52-53.
Saraf P. Phytochemical and antimicrobial studies of medicinal plant Costus speciosus
(Koen.). E-J Chem
2010; 7(S1): S405-S413.
Dadsena R, Sahu NK, Agrwal S, Kumar A. Phytochemical analysis of three endangered Plants (Costus specious, Gloriossa superba
Linn Andrauvolfia serpentine
(Linn) Benth) from Kanker district of Chhattisgarh, India. Bioscan
2013; 8(2): 655-659.
Eliza J, Daisy P, Ignacimuthu S, Duraipandiyan V. Antidiabetic and antilipidemic effect of eremanthin from Costus speciosus
(Koen.)Sm., in STZ-induced diabetic rats. Chem Biol Interact
2009; 182(1): 67-72.
Verma N, Khosa RL. Evaluation of protective effects of ethanolic extract of Costus speciosus
(Koenig) sm. rhizomes on carbon tetrachloride induced hepatotoxicity in rats. Indian J Nat Prod Resour
2008; 8(2): 123-126.
Srivastava S, Singh P, Mishra G, Jha KK, Khosa RL. Costus speciosus
(Keukand): A review. Der Chem Sin
2011; 2(1): 118-128.
Yasodha S, Nivedhana Arthi P, Agarwal A. Antifertility activity of ethanolic extract of Costus pictus
rhizome in female rats. Sch J Appl Med Sci
2017; 5(1A): 62-64.
Binny K, Kumar GS, Thomas D. Anti-inflammatory and antipyretic properties of the rhizome of Costus speciosus
(koen.) SM. J Basic Clin Pharm
2010; 1(3): 177-181.
Neshe SA, Arefin S, Hussain MS, Das A, Karmakar P, Hossain MS. Safety evaluation of chocolate brown dye in Swiss albino mice. J Nutr Disord Ther
2016; 6(3). Doi:10.4172/2161-0509.1000195.
Lister RG. The use of a plus-maze to measure anxiety in the mouse. Psychopharmacology (Berl)
1987; 92(2): 180-185.
Narasingam M, Vijeepallam K, Mohamed Z, Pandy V. Anxiolytic- and antidepressant-like activities of a methanolic extract of Morinda citrifolia
Linn. (noni) fruit in mice: Involvement of benzodiazepine-GABAAergic, serotonergic and adrenergic systems. Biomed Pharmacother
944-952. Doi: 10.1016/j.biopha.2017.11.148.
File SE, Wardill AG. Validity of head-dipping as a measure of exploration in a modified hole-board. Psychopharmacologia
1975; 44(1): 53-59.
Bourin M, Hascoët M. The mouse light-dark box test. Eur J Pharmacol
2003; 463(1-3): 55-65.
Moniruzzaman M, Rahman MA, Ferdous A. Evaluation of sedative and hypnotic activity of ethanolic extract of Scoparia dulcis
Linn. Evid Based Complement Alternat Med
Chellian R, Pandy V, Mohamed Z. Biphasic effects of α-asarone on immobility in the tail suspension test: Evidence for the involvement of the noradrenergic and serotonergic systems in its antidepressant-like activity. Front Pharmacol
72. Doi: 10.3389/fphar.2016.00072.
Steru L, Chermat R, Thierry B, Simon P. The tail suspension test: A new method for screening antidepressants in mice. Psychopharmacology (Berl)
1985; 85(3): 367-370.
Chellian R, Pandy V, Mohamed Z. Alpha-asarone attenuates depressionlike behavior in nicotine-withdrawn mice: Evidence for the modulation of hippocampal pCREB levels during nicotine-withdrawal. Eur J Pharmacol
10-16. Doi: 10.1016/j.ejphar.2017.10.025
Porsolt RD, Anton G, Blavet N, Jalfre M. Behavioural despair in rats: A new model sensitive to antidepressant treatments. Eur J Pharmacol
Kessler R, Birnbaum H, Shahly V, Bromet E, Hwang I, McLaughlin K, et al. Age differences in the prevalence and co-morbidity of DSM-IV major depressive episodes: Results from the WHO World Mental Health Survey Initiative. Depress Anxiety
2010; 27(4): 351-364.
Collimore KC, Rector NA. Treatment of anxiety disorders with comorbid depression: A survey of expert CBT clinicians. Cogn Behav Pract
2014; 21(4): 485-493.
Wei XY, Yang JY, Wang JH, Wu CF. Anxiolytic effect of saponins from Panax quinquefolium
in mice. J Ethnopharmacol
2007; 111(3): 613-618.
Foyet HS, Tsala DE, Bouba AA, Hritcu L. Anxiolytic and antidepressant- like effects of the aqueous extract of Alafia multiflora
stem barks in rodents. Adv Pharmacol Sci
Barua CC, Roy JD, Buragohain B, Barua AG, Borah P, Lahkar M. Anxiolytic effect of hydroethanolic extract of Drymaria cordata
L Willd. Indian J Exp Biol
Takeda H, Tsuji M, Matsumiya T. Changes in head-dipping behavior in the hole-board test reflect the anxiogenic and/or anxiolytic state in mice. Eur J Pharmacol
1998; 350(1): 21-29.
Belzung C, Misslin R, Vogel E. Anxiogenic effects of methyl-/3- carboline-3-carboxylate in a light/dark choice situation. Pharmacol Biochem Behav
1987; 28(1): 29-33.
Dey P, Chandra S, Chatterjee P, Bhattacharya S. Neuropharmacological properties of Mikania scandens
(L.) Willd. (Asteraceae). J Adv Pharm Technol Res
2011; 2(4): 255-259.
Abedin F, Hussain MS, Islam A, Sen N, Das A, Kar A, et al. Thrombolytic, CNS depressant and anti-diarrhoeal activities of ethanolic extract of bark of Syzygium cumini
L. skeels: An in-vivo
study. J Pharm Nutr Sci
2018; 8(3): 129-136.
Kumar K, Sharma S, Kumar P, Deshmukh R. Therapeutic potential of GABA(B) receptor ligands in drug addiction, anxiety, depression and other CNS disorders. Pharmacol Biochem Behav
Sultana T, Mannan MA, Ahmed T. Evaluation of central nervous system (CNS) depressant activity of methanolic extract of Commelina diffusa
Burm. in mice. Clin Phytoscience
2018; 4(5). Doi: 10.1186/s40816-018- 0063-1.
Bhosale U, Yegnanarayan R, Prachi P, Zambare M, Somani RS. Study of CNS depressant and behavioral activity of an ethanol extract of Achyranthes aspera
(chirchita) in mouse model. Ann Neurosci
2011; 18(2): 44-47.
Gahlot K, Lal VK, Jha S. Anticonvulsant potential of ethanol extracts and their solvent partitioned fractions from Flemingia strobilifera
root. Pharmacognosy Res
2013; 5(4): 265-270.
Shams-Ud-Doha K, Al Mahmud Z, Bachar SC, Qais N. Antinociceptive, anti-inflammatory, antimicrobial and central nervous system depressant activities of ethanolic extract of leaves and roots of Gomphostemma parviflorum
var. parviflorum wall. Pharmacognosy Res
2013; 5(4): 233-240.
Huang F, Xiong Y, Xu L, Ma S, Dou C. Sedative and hypnotic activities of the ethanol fraction from Fructus Schisandrae in mice and rats. J Ethnopharmacol
2007; 110(3): 471-475.
Subarnas A, Tadano T, Nakahata N, Arai Y, Kinemuchi H, Oshima Y, et al. A possible mechanism of antidepressant activity of beta-amyrin palmitate isolated from Lobelia inflates
leaves in the forced swimming test. Life Sci
1993; 52(3): 289-296.
Surana AR, Wagh RD. Phytochemical analysis and antidepressant activity of Ixora coccinea
extracts in experimental models of depression in mice. Turkish J Pharm Sci
2018; 15(2): 130-135.
[Table 1], [Table 2], [Table 3], [Table 4]
|This article has been cited by|
||CNS anti-depressant, anxiolytic and analgesic effects of Ganoderma applanatum (mushroom) along with ligand-receptor binding screening provide new insights: Multi-disciplinary approaches
| ||S M Moazzem Hossen,Mohammad Jahedul Islam,Md. Rabiul Hossain,Anik Barua,Md. Giash Uddin,Nazim Uddin Emon |
| ||Biochemistry and Biophysics Reports. 2021; 27: 101062 |
|[Pubmed] | [DOI]|
||Exploration of in vitro thrombolytic, anthelminthic, cytotoxic and in vivo anxiolytic potentials with phytochemical screening of flowers of Brassica nigra
| ||Mohammad Sarowar Uddin,Md. Shalahuddin Millat,Mohammad Safiqul Islam,Md. Saddam Hussain,Md. Giash Uddin,Shafayet Ahmed Siddiqui,Mahmuda Ferdous |
| ||Future Journal of Pharmaceutical Sciences. 2020; 6(1) |
|[Pubmed] | [DOI]|
||Evaluation of anxiolytic and hypoglycemic potential of Cissus adnata Roxb. in animal model
| ||Mohammed Shamim Hasan,Md. Giash Uddin,Mohammed Shoibe,Abdullah Al Mahmud,Sujan Banik |
| ||Journal of Complementary and Integrative Medicine. 2019; 0(0) |
|[Pubmed] | [DOI]|