|Year : 2015 | Volume
| Issue : 6 | Page : 610-615
An evaluation of the protective role of Ficus racemosa Linn. in streptozotocin-induced diabetic neuropathy with neurodegeneration
Nilay D Solanki1, Shailesh K Bhavsar2
1 Department of Pharmacology, Ramanbhai Patel College of Pharmacy, Charotar University of Science and Technology, Changa, Gujarat, India
2 Department of Pharmacology and Toxicology, Vanbandhu College of Veterinary Science and Animal Husbandry, Navsari Agricultural University, Navsari, Gujarat, India
|Date of Submission||09-May-2015|
|Date of Decision||01-Jul-2015|
|Date of Acceptance||14-Oct-2015|
|Date of Web Publication||17-Nov-2015|
Prof. Nilay D Solanki
Department of Pharmacology, Ramanbhai Patel College of Pharmacy, Charotar University of Science and Technology, Changa, Gujarat
Source of Support: None, Conflict of Interest: None
Objective: Ficus racemosa (FR) is one of the herbs mentioned in the scriptures of the Ayurveda as Udumbara with high medicinal value. The objective of this study was to estimate the protective effect of FR against streptozotocin (STZ) induced diabetic neuropathy with neurodegeneration (DNN).
Materials and Methods: Diabetes was induced in Wistar rats with STZ and were divided into six groups namely diabetic vehicle control, FR (four) and glibenclamide (one) treated rats; while one group was of normal control rats. After the 4th week of diabetes, induction treatment was started for further 28 days (5th to 8th week) with FR aqueous extract (250 mg/kg and 500 mg/kg) and ethanolic extract (200 mg/kg and 400 mg/kg). Investigation of DNN was carried out through biochemical and behavioral parameter assessment in rats.
Results: Study showed a significant fall in glycosylated hemoglobin (HbA1c) and blood glucose level by the treatment of FR in diabetic rats. Antioxidant potential of FR showed a great rise in superoxide dismutase, catalase content and reduction observed in serum nitrite level; while significant fall in lipid peroxidation level and of C-reactive protein was observed in FR treated diabetic rats. Further FR treated diabetic rats also showed marked improvement in tail flick latency, pain threshold, the rise in locomotion and fall latency period.
Conclusion: Treatment with FR shows protection in the multiple pathways of DNN by improving blood glucose, HbA1c, biochemical, and behavioral parameters, which suggest the protective role of FR in the reversal of DNN.
Keywords: Behavioral parameters, biochemical parameters, diabetes mellitus, diabetic neuropathy with neurodegeneration, Ficus racemosa
|How to cite this article:|
Solanki ND, Bhavsar SK. An evaluation of the protective role of Ficus racemosa Linn. in streptozotocin-induced diabetic neuropathy with neurodegeneration. Indian J Pharmacol 2015;47:610-5
|How to cite this URL:|
Solanki ND, Bhavsar SK. An evaluation of the protective role of Ficus racemosa Linn. in streptozotocin-induced diabetic neuropathy with neurodegeneration. Indian J Pharmacol [serial online] 2015 [cited 2023 Feb 3];47:610-5. Available from: https://www.ijp-online.com/text.asp?2015/47/6/610/169579
| » Introduction|| |
Diabetes mellitus is a metabolic disease which damage different bodily organs, causing kidney failure, vision loss, autonomic and peripheral neuropathy, peripheral vascular disease, myocardial infarction, and cerebrovascular disease with stroke. Diabetes affects the central nervous system and produce disturbances such as behavioral changes, autonomic dysfunctions, altered neuroendocrine functions, and neurotransmitter alterations and thus leading to end organ damage., Various pathways involved in the pathogenesis of diabetic neuropathy and degeneration are polyol, hexosamine, protein kinase C, advanced glycation, poly (ADP-ribose) polymerase, oxidative stress, and inflammation. Oxidative stress and inflammation play a crucial role in the development and progression of late-stage complications of diabetes, an acute phase reactant C-reactive protein (CRP) level rises dramatically during inflammatory processes. The antioxidant defenses in humans are superoxide dismutase (SOD), catalase (CAT), and glutathione peroxidase. Lipid peroxidation (LPO) was one of the characteristic features of the chronic diabetic condition. Plants have been the major source of the treatment for diabetes in the Indian system of medicine and other ancient systems in the world. Ficus racemosa Linn. (FR) (Family Moraceae) is one of the plants mentioned in the ancient scriptures of Ayurveda. The aim of the present study was to investigate the protective role of FR Linn. in streptozotocin (STZ) induced diabetic neuropathy and neurodegeneration (DNN), which has not been evaluated so far.
| » Materials and Methods|| |
Drugs and Chemicals
All reagents were analytical grades. Biochemical kits were purchased from Span diagnostics, India. STZ was obtained from Sigma chemicals, India. Glibenclamide (GL) was obtained as gratis sample.
Extraction Methods of Ficus racemosa
FR stem bark was collected from the Directorate of medicinal and Aromatic Plants Research, Gujarat. The stem bark was shade dried and converted into powder form by the milling process. An amount of 50 g of powder was dissolved in 3/4th of water, and the mixture was boiled with the temperature not exceeding 50–60°C till the volume of water came down to one-fourth. The mixture was cooled, and concentrated portion was considered as aqueous extract. A total 200 g of powder was dissolved in 99.5% strength with 2/3rd of ethyl alcohol mixed well and refluxed for 3–4 days (3–4 h/day). The alcoholic portion was transferred in rota-vapor (temp of bath 60°C, RPM – 110, Vacuum – 100) until complete drying of alcoholic extract. The aqueous extract was prepared in 10% tween 20 solution prepared in double distilled water while ethanolic extracts were prepared in 5% gum acacia solution for oral administration. Both the vehicles utilized for aqueous and ethanolic extract were inert.
Animals and Experimental Protocol
The animal protocol was approved by the Institutional Animal Ethics Committee. Male Wistar rats (300 ± 50 g) were provided the standard pelleted diet and ad libitum water, were kept at environmental temperature (23°C ± 3°C) and under 12 h light-dark cycle. The animals were acclimatized to the experimental conditions a week before the study. Acute toxicity study of FR was performed with a dose level of 2000 mg/kg, which formed the basis for dose selection in the efficacy study.
Induction of Diabetic Complication with Treatment Schedule
Diabetes was induced in overnight fasted rats by a single intraperitoneal injection of fresh STZ , (60 mg/kg body weight) in citrate buffer (0.1M, pH 7.4). After 48 h of STZ injection, fasting blood samples were withdrawn from tail vein and blood glucose level was measured by use of a glucometer (Accu-Chek, Johnson and Johnson, India). The animals having fasting blood glucose level ≥230 mg/dl were randomized in groups. The development of DNN was confirmed by basal nociceptive reaction at the 4th week of STZ injection, and all treatments were started thereafter from 5th to 8th week. GL is widely used as second-line therapy in diabetes and can lower glycosylated hemoglobin (HbA1c) by 1–2%, several research reports had mentioned the use of GL as a positive control.,, At the end of 8th week, behavioral analysis were done and the blood sample was collected, while brain and sciatic nerve were isolated and washed with ice-cold saline, then homogenate was prepared and stored at –80°C till further analysis. No mortality was observed during the study period.
The animals were divided into seven groups (n = 5):
- Normal control (NC) animals received saline
- Diabetic control (DC) animals received saline
- FR aqueous extract treated diabetic animals (250 mg/kg) p.o (DAFR-250)
- FR aqueous extract treated diabetic animals (500 mg/kg) p.o (DAFR-500)
- FR ethanolic extract treated diabetic animals (200 mg/kg) p.o (DEFR-200)
- FR ethanolic extract treated diabetic animals (400 mg/kg) p.o (DEFR-400)
- GL-treated diabetic rats (2.5 mg/kg) (DGLY).
Analysis of blood glucose and glycosylated hemoglobin level
The blood glucose level was analyzed with glucometer using glucose reagent strip while HbA1c level was measured as reference cited.
Serum protein level and C-reactive protein
Serum protein (SP) level (g/dl) was estimated by a method as per assessment kit. CRP level (mg/l) was determined by particle enhanced immunoturbidometry method.
Serum antioxidant catalase and superoxide dismutase
CAT activity of serum samples was expressed in μmol H2O2 utilized per min/mg of protein. SOD level in serum was expressed as mU of SOD/mg protein.
Serum nitrite level
The serum nitrite level was estimated using greiss reagent which served as an indicator of nitric oxide production.
Tissue homogenate level of malondialdehyde
LPO product as malondialdehyde (MDA) level estimated in tissue homogenate by method cited in reference.
Tail immersion (hot water) test
The tail of the rat was immersed in a hot water bath (55°C ± 0.5°C) until withdrawal or signs of struggle were observed (cutoff 10 s). Shortening of the tail-withdrawal time indicated hyperalgesia.
Hot plate test
In this test, animals were individually placed on a hot plate with the temperature adjusted to 43°C ± 1°C. The latency to the first sign of paw licking or jump response to avoid the heat was taken as an index of the pain threshold.
Motor coordination activity
The motor coordination and performance of each rat was evaluated using rota-rod apparatus. Latency to fall from the rotating bar was registered in seconds.
Photoactometer test was performed to study the effect of drug treatment on spontaneous motor activity and cutoff of the photocell beam was recorded.
Values in the result were expressed as a mean ± standard error of the mean. Differences between groups mean were estimated using one-way analysis of variance. Paired t-test was applied for the comparison of groups at different time interval. The result was considered statistically significant at P < 0.05, 0.01, and 0.001.
| » Results|| |
STZ injected Wistar rats had produced cardinal signs of diabetes, i.e., weekly change in body weight [Figure 1], polyphagia, and polydipsia [Table 1], which persisted throughout the period of study.
|Figure 1: Effect of Ficus racemosa aqueous and ethanolic extracts administration on weekly changes in body weight (g). Each value was considered as mean ± standard error of mean. (n = 5) statistical significant difference was mentioned for Ficus racemosa treated groups (P < 0.05) as compared to diabetic control animals|
Click here to view
|Table 1: Effect of FR Linn. Aqueous and ethanolic extracts administration on food and water intake|
Click here to view
Effect of Ficus racemosa on Body Weight, Food, and Water Intake
Chronic treatment with FR significantly in diabetes prevented weight loss as compared to DC rats [Figure 1]. FR treated diabetic rats also showed a reduction in food consumption and increased water intake during the study period.
Effect of Ficus racemosa on Biochemical Markers
Effect of Ficus racemosa on blood glucose and glycosylated hemoglobin level
Sustained hyperglycemia was observed in STZ induced diabetic rats during the study. There was significant reduction seen in blood glucose level of FR treated diabetic animals as compared to DC rats [Figure 2]. HbA1c level was significantly increased in diabetic animals (8.14 ± 0.34), while aqueous (5.66 ± 0.78, 5.44 ± 0.73) and ethanolic extract of FR (6.38 ± 1.02, 5.47 ± 1.84) treated animals showed a significant reduction in HbA1c level [Table 2].
|Figure 2: Effect of Ficus racemosa aqueous and ethanolic extracts administration on blood glucose analysis before and after the treatment each value was considered as mean ± standard error of mean. (n = 5) statistical significant difference was mentioned of Ficus racemosa, glibenclamide treated and normal control group (**P < 0.01) compared to diabetic control animals statistical significant difference was mentioned of diabetic control (##P < 0.01) as compared to normal control group|
Click here to view
|Table 2: Effect of FR Linn. aqueous and ethanolic extracts administration on SP, catalase, SOD, CRP, nitrite, tissue MDA levels and HbA1c estimation|
Click here to view
Effect of Ficus racemosa on Antioxidant Level
Antioxidant enzyme (CAT and SOD) levels were significantly reduced in diabetic animals (P < 0.05) as compared to normal animals, while FR treated groups showed significant rise in CAT and SOD enzyme levels as of DC rats.
Effect of Ficus racemosa on Serum Protein, C-reactive Protein, and Nitrite Level
Protein present in the blood was significantly higher in diabetic rats as compared to NC animals [Table 2]. Treatment with FR showed a significant reduction in SP content as compared to DC rats. CRP levels were significantly increased in diabetic rats as compared to normal rats, while FR treated diabetic rats showed a significant reduction in CRP level as compared to DC rats [Table 2].
Nitrite levels were significantly increased in diabetic rats as compared to NC rats, while FR treated animals showed a significant reduction in nitrite level as compared to DC rats [Table 2].
Effect of Ficus racemosa on Tissue Malondialdehyde Level
Tissue MDA level was significantly raised in brain and nerve tissues of diabetic rats. Two-fold decrease in the level of brain MDA was observed in FR (aqueous extract) treated diabetic rats, while four-fold decrease in brain MDA level were observed in FR (ethanolic extract) treated diabetic rats as compared to DC rats [Table 2]. Nerve MDA level were reduced four-fold with FR treated (ethanolic extract) diabetic rats as compared to DC rats.
Effect of Ficus racemosa on Behavioral Markers
STZ injected rats had nociceptive threshold significantly lower than NC rats as observed by tail immersion test and hot plate assay. FR treated diabetic rats exhibited a rise in the tail flick latency as compared to DC rats [Table 3]. FR aqueous extract treated group showed significantly improved pain threshold, while FR ethanolic extract treated group showed double fold rise in pain threshold as compared to DC rats [Table 3]. Diabetic animals showed reduced locomotion (lo) ability as observed in a number of cut off significantly different from NC rats (100.2 ± 2.03). FR treated diabetic animals showed a significant rise in lo time as compared to DC rats [Table 3]. The rota-rod test experiment demonstrated the impairment of the motor function and coordination in the diabetic rats with a significant reduction in fall off time as compared to NC rats. FR extract treated diabetic rats showed a significant increase in fall off time as compared to diabetic animals [Table 3].
|Table 3: Effect of FR Linn. aqueous and ethanolic extracts administration on photoactometer, rotarod test, hot plate assay and tail immersion test|
Click here to view
| » Discussion|| |
STZ causes direct DNA damage to the pancreatic islets of beta cells, which leads to hyperglycemic state. Increase in blood glucose and HbA1c levels following STZ treatment observed in our study was supported by other work.,Coscinium fenestratum stem and Catharanthus roseus brought back the status of blood glucose and HbA1c to normal range in diabetic rats, supported our study results. Alteration in antioxidant defense in the diabetic rats was evidenced by a significant reduction in serum antioxidant enzyme activity in diabetic rats. The decrease in antioxidant enzymes activity in the hyperglycemic rats could be due to oxidative stress induced inactivation  which was observed in present study. Antioxidant levels were increased with FR treatment in DNN supported by result of carnitine and lipoic acid had reduced free radical production and increased in antioxidant status thereby lowering oxidative stress, while ginger had significantly improved the level of SOD, CAT in diabetic rats. The excessive production of superoxide and peroxynitrite in sciatic nerve have been linked with altered vaso-relaxation responsible for nerve perfusion irregularities. In hyperglycemia induced oxidative injury, key mediator is peroxynitrite formed by the combination of superoxide with nitric oxide that exerts detrimental effects on the nerve tissue leading to neuropathic pain. Thus formed peroxynitrite further initiates the pathways implicated in the development of diabetes neuropathy and degeneration. Present study showed reduced nitrite level by FR in diabetic rats, supported by a work showed that reduced neural nitrite level in naringin-treated diabetic rats. In another study, cannabis exhibited significantly lower levels of nitrite in diabetic condition. CRP, an acute phase reactant, was a highly sensitive marker of inflammation. Treatment with FR extracts showed anti-inflammatory potential, which is supported by results of berberine, which had reduced plasma CRP levels. LPO was one of the characteristic features of chronic diabetes. The overall effect of LPO was to decrease the membrane fluidity, deformability, visco elasticity of tissues, which was improved by treatment with FR extracts in diabetic rats, result of other studies showed decreased LPO level in diabetic rats when treated by ginger  and Erythrina variegate also showed reduction in basal LPO as compared to DC. The nociceptive threshold was significantly lower in diabetic animals than nondiabetic animals indicating that diabetics exhibited thermal hyperalgesia. Diabetic rats showed a significant reduction in paw withdrawal threshold, which indicates the development of hyperalgesia. Present study revealed that treatment with FR prevents allodynia which further reduces neuropathic pain in diabetic rats, in scientific evidence naringin-treated diabetic rats attenuated reduced mean tail withdrawal latency as compared to diabetic rats. Present study also evaluated the behavioral response in motor and lo performance of diabetic and NC rats through rota-rod and photoactometer test. Diabetic rats showed lower fall off time from the rotating rod when compared to NC and suggesting impairment in their ability to integrate sensory input with appropriate motor commands to balance their posture as showed in present study supported by literature. Present study showed reduced motor performance (mp) and lo in STZ-induced diabetic rats, and FR treated rats showed improvement for mp and lo in diabetic rats. In one study, fall latency was improved, motor incoordination was prevented, and lo counts were improved when diabetic rats treated by the extract of Pakinsonia aculeate  supports our study results.
| » Conclusion|| |
The data of present study suggest that FR exhibit protective effect by reducing complications of DNN through preventing a rise in glycated hemoglobin content, reduced oxidative-nitrosative stress level, and decreased early inflammation level. FR treatment also showed excellent antioxidant potential with a low level of LPO thus provided protection in diabetic tissue. Behavioral aspects were improved during treatment by FR in diabetic animals. FR may be considered as a future option due to varieties of pharmacological actions with proven results in DNN for its reversal. However, further studies are required for the better understanding of the mechanism of action of FR.
Ramanbhai Patel College of Pharmacy, Charotar University of Science and Technology.
Financial Support and Sponsorship
Ramanbhai Patel College of Pharmacy.
Conflicts of Interest
There are no conflicts of interest.
| » References|| |
Zhao Y, Ye W, Boye KS, Holcombe JH, Hall JA, Swindle R. Prevalence of other diabetes-associated complications and comorbidities and its impact on health care charges among patients with diabetic neuropathy. J Diabetes Complications 2010;24:9-19.
Nishikawa T, Edelstein D, Du XL, Yamagishi S, Matsumura T, Kaneda Y, et al.
Normalizing mitochondrial superoxide production blocks three pathways of hyperglycaemic damage. Nature 2000;404:787-90.
Brands AM, Kessels RP, de Haan EH, Kappelle LJ, Biessels GJ. Cerebral dysfunction in type 1 diabetes: Effects of insulin, vascular risk factors and blood-glucose levels. Eur J Pharmacol 2004;490:159-68.
Schalkwijk CG, Poland DC, van Dijk W, Kok A, Emeis JJ, Dräger AM, et al.
Plasma concentration of C-reactive protein is increased in type I diabetic patients without clinical macroangiopathy and correlates with markers of endothelial dysfunction: Evidence for chronic inflammation. Diabetologia 1999;42:351-7.
Dong Q, Wright JR. Expression of C-reactive protein by alveolar macrophages. J Immunol 1996;156:4815-20.
Solanki ND, Bhavsar SK. Toxicological evaluation of the aqueous fraction of Ficus racemosa
and Bauhinia variegate
bark in Rats. Int J Toxicol Pharmacol Res 2014;6:80-5.
Ahmed D, Kumar V, Verma A, Shukla GS, Sharma M. Antidiabetic, antioxidant, antihyperlipidemic effect of extract of Euryale ferox
salisb. with enhanced histopathology of pancreas, liver and kidney in streptozotocin induced diabetic rats. Springerplus 2015;4:315.
Goyal BR, Solanki N, Goyal RK, Mehta AA. Investigation into the cardiac effects of spironolactone in the experimental model of type 1 diabetes. J Cardiovasc Pharmacol 2009;54:502-9.
Lahiri SW. Management of type 2 diabetes: What is the next step after metformin. Clin Diabetes 2012;30:272-5.
Manoharan S, Umadevi S, Jayanthi S, Baskaran N. Antihyperglycemic effect of Coscinium fenestratum
and Catharanthus roseus
in alloxan-induced diabetic rats. Int J Nutr Pharmacol Neurol Dis 2011;1:189-93.
Shanmugam KR, Mallikarjuna K, Kesireddy N, Sathyavelu Reddy K. Neuroprotective effect of ginger on anti-oxidant enzymes in streptozotocin-induced diabetic rats. Food Chem Toxicol 2011;49:893-7.
Miedema K. Towards worldwide standardisation of HbA1c determination. Diabetologia 2004;47:1143-8.
Koller A. Proteins. In: Clinical Chemistry: Theory, Analysis, and Correlation. St. Louis: Mosby Company; 1984. p. 1268-327.
Hokama Y, Nakamura RM. C-reactive protein: Current status and future perspectives. J Clin Lab Anal 1987;1:15-27.
Aebi H. Catalase in vitro
. Methods Enzymol 1984;105:121-6.
Misra HP, Fridovich I. The role of superoxide anion in the autoxidation of epinephrine and a simple assay for superoxide dismutase. J Biol Chem 1972;247:3170-5.
Griess P. Bemerkungen zu der abhandlung der H. H. Weselsky und Benedikt “Ueber einige azoverbindungen.” Chem Ber 1879;12:426.
Ohkawa H, Ohishi N, Yagi K. Assay for lipid peroxides in animal tissues by thiobarbituric acid reaction. Anal Biochem 1979;95:351-8.
Kanaan SA, Saadé NE, Haddad JJ, Abdelnoor AM, Atweh SF, Jabbur SJ, et al.
Endotoxin-induced local inflammation and hyperalgesia in rats and mice: A new model for inflammatory pain. Pain 1996;66:373-9.
Dunham NW, Miya TS. A note on a simple apparatus for detecting neurological deficit in rats and mice. J Am Pharm Assoc Am Pharm Assoc 1957;46:208-9.
Goddard M, Zheng Y, Darlington CL, Smith PF. Locomotor and exploratory behavior in the rat following bilateral vestibular deafferentation. Behav Neurosci 2008;122:448-59.
Frankish N, de Sousa Menezes F, Mills C, Sheridan H. Enhancement of insulin release from the beta-cell line INS-1 by an ethanolic extract of Bauhinia variegata and its major constituent roseoside. Planta Med 2010;76:995-7.
Seven A, Guzel S, Seymen O, Civelek S, Bolayirli M, Uncu M, et al.
Effects of Vitamin E supplementation on oxidative stress in streptozotocin induced diabetic rats: Investigation of liver and plasma. Yonsei Med J 2004;45:703-10.
Savitha S, Tamilselvan J, Anusuyadevi M, Panneerselvam C. Oxidative stress on mitochondrial antioxidant defense system in the aging process: Role of DL-alpha-lipoic acid and L-carnitine. Clin Chim Acta 2005;355:173-80.
Coppey LJ, Gellett JS, Davidson EP, Yorek MA. Preventing superoxide formation in epineurial arterioles of the sciatic nerve from diabetic rats restores endothelium-dependent vasodilation. Free Radic Res 2003;37:33-40.
Shukla PK, Tang L, Wang ZJ. Phosphorylation of neurogranin, protein kinase C, and Ca2±/calmodulin dependent protein kinase II in opioid tolerance and dependence. Neurosci Lett 2006;404:266-9.
Ceriello A. Oxidative stress and diabetes-associated complications. Endocr Pract 2006;12 Suppl 1:60-2.
Kandhare AD, Raygude KS, Ghosh P, Ghule AE, Bodhankar SL. Neuroprotective effect of naringin by modulation of endogenous biomarkers in streptozotocin induced painful diabetic neuropathy. Fitoterapia 2012;83:650-9.
Arora A, Taliyan R, Sharma PL. Ameliorative potential of cannabis sativa extract on diabetes induced neuropathic pain in rats. Int J Pharm Sci Res 2010;1:91-9.
Chen Y, Wang Y, Zhang J, Sun C, Lopez A. Berberine improves glucose homeostasis in streptozotocin-induced diabetic rats in association with multiple factors of insulin resistance. ISRN Endocrinol 2011;2011:519371.
Anupama V, Narmadha R, Gopalakrishnan VK, Devaki K. Enzymatic alteration in the vital organs of streptozotocin diabetic rats treated with aqueous extract of Erythrina variegata
bark. Int J Pharm Pharm Sci 2012;4:134-47.
Hundekari GI, Shahana S, Shukoor MA, Nagappa AN. Antidiabetic activity of aqueous extract of parkinsonia aculeata in alloxan induced diabetic rats, with emphasis on diabetic complications. Int J Pharma Bio Sci 2013;4:533-41.
[Figure 1], [Figure 2]
[Table 1], [Table 2], [Table 3]
|This article has been cited by|
||Antioxidative hypoglycemic herbal medicines with in vivo and in vitro activity against C-reactive protein; a systematic review
| ||Maryam Mirahmad, Shahrzad Mohseni, Ozra Tabatabaei-Malazy, Fataneh Esmaeili, Sudabeh Alatab, Roodabeh Bahramsoltani, Hanieh-Sadat Ejtahed, Husseyn Qulami, Zahra Bitarafan, Babak Arjmand, Elahe Nazeri |
| ||Phytomedicine. 2022; : 154615 |
|[Pubmed] | [DOI]|
||Isolation of Thymol from Trachyspermum ammi Fruits for Treatment of Diabetes and Diabetic Neuropathy in STZ-Induced Rats
| ||Neetu Sachan, Nikita Saraswat, Phool Chandra, Mohammad Khalid, Atul Kabra, Riaz Ullah |
| ||BioMed Research International. 2022; 2022: 1 |
|[Pubmed] | [DOI]|
||Sphaeranthus indicus Linn ameliorates streptozotocin-induced experimental diabetic neuropathy by targeting oxidative stress-mediated alterations
| ||Vishal B. Jadhav, Jai Singh Vaghela |
| ||Future Journal of Pharmaceutical Sciences. 2022; 8(1) |
|[Pubmed] | [DOI]|
||Alleviating effect of Ficus racemosa in high-fat-high-fructose diet-induced non-alcoholic fatty liver disease
| ||Nilay D. Solanki, Kirti Vadi, Sandip Patel |
| ||Indian Journal of Physiology and Pharmacology. 2021; 65: 12 |
|[Pubmed] | [DOI]|
||Neuroprotective Effects of Dried Tubers of Aconitum napellus
| ||Ambreen Shoaib, Hefazat Hussain Siddiqui, Rakesh Kumar Dixit, Sahabjada Siddiqui, Badrud Deen, Andleeb Khan, Salman H. Alrokayan, Haseeb A. Khan, Parvaiz Ahmad |
| ||Plants. 2020; 9(3): 356 |
|[Pubmed] | [DOI]|
||Diabetic encephalopathy causes the imbalance of neural activities between hippocampal glutamatergic neurons and GABAergic neurons in mice
| ||Chun Wang, Juan Li, Shidi Zhao, Li Huang |
| ||Brain Research. 2020; 1742: 146863 |
|[Pubmed] | [DOI]|
Beneficial effects of n-hexane bark extract of
L. on diabetic peripheral neuropathy
| ||Ambreen Shoaib, Badruddeen, Rakesh Kumar Dixit, Magdah Ganash, George Barreto, Ghulam Md Ashraf, Hefazat Hussain Siddiqui |
| ||Journal of Cellular Biochemistry. 2019; 120(10): 16524 |
|[Pubmed] | [DOI]|
||PROTECTIVE ROLE OF FICUS RACEMOSA IN DIABETES INDUCED NEUROPATHY: STRUCTURAL AND FUNCTIONAL EVIDENCES
| ||N Solanki, S. K Bhavsar |
| ||INDIAN DRUGS. 2017; 54(11): 58 |
|[Pubmed] | [DOI]|