IPSIndian Journal of Pharmacology
Home  IPS  Feedback Subscribe Top cited articles Login 
Users Online : 4287 
Small font sizeDefault font sizeIncrease font size
Navigate Here
Resource Links
 »  Similar in PUBMED
 »  Search Pubmed for
 »  Search in Google Scholar for
 »Related articles
 »  Article in PDF (1,695 KB)
 »  Citation Manager
 »  Access Statistics
 »  Reader Comments
 »  Email Alert *
 »  Add to My List *
* Registration required (free)

In This Article
 »  Abstract
 » Introduction
 »  Materials and Me...
 » Results
 » Discussion
 » Acknowledgment
 »  References
 »  Article Figures
 »  Article Tables

 Article Access Statistics
    PDF Downloaded164    
    Comments [Add]    
    Cited by others 4    

Recommend this journal


 Table of Contents    
Year : 2015  |  Volume : 47  |  Issue : 4  |  Page : 430-435

Efficacy of Spirulina platensis in improvement of the reproductive performance and easing teratogenicity in hyperglycemic albino mice

Department of Zoology, Nagaland University, Lumami, Nagaland, India

Date of Submission10-Jun-2014
Date of Decision20-Jul-2014
Date of Acceptance25-Jun-2015
Date of Web Publication21-Jul-2015

Correspondence Address:
Dr. Pranay Punj Pankaj
Department of Zoology, Nagaland University, Lumami, Nagaland
Login to access the Email id

Source of Support: None, Conflict of Interest: None

DOI: 10.4103/0253-7613.161271

Rights and Permissions

 » Abstract 

Objectives: The present study evaluates the therapeutic efficacy of cell suspension of Spirulina platensis (SP) on estrous cycle, fetal development and embryopathy in alloxan (AXN) induced hyperglycemic mice.
Materials and Methods: Diabetes was induced by intra-peritoneal administration of AXN. Mice with blood glucose level above 200 mg/dl were divided into Group I (control), Group II (diabetic control), Group III (diabetic control mice fed with SP), and Group IV (control mice fed with SP). Litter counts, estrous cycles, percent survival of litter, and gestation length were recorded.
Results: In hyperglycemic mice, a significant (P < 0.05) increase in duration of diestrus (14.48%), estrus (84.21%), and metestrus (164.15%) with concomitant decrease in proestrus phase by 26.13% was recorded when compared with control. Reduction in litter count and survival of litter was 68.67% and 88.38%, respectively, whereas gestation length increased to 14.51% day in diabetic mice, but recovery in these parameters was observed (P < 0.05) when subjected to SP treatment. SP resulted in increased fertility rate from 77.5% to 82.5% and dropped off resorption of the fetus to 33.73% while the survival rate of offspring of diabetic mice went up to 88.89% from 83.61%.
Conclusions: These findings suggest that SP is effective in improving the reproductive performance and easing teratogenic effects in diabetic mice and hence warrants further detailed dose-dependent studies to understand its mechanism of action.

Keywords: Diabetes, estrous cycle, fertility rate, fetal development, gestation length, Spirulina platensis

How to cite this article:
Pankaj PP. Efficacy of Spirulina platensis in improvement of the reproductive performance and easing teratogenicity in hyperglycemic albino mice. Indian J Pharmacol 2015;47:430-5

How to cite this URL:
Pankaj PP. Efficacy of Spirulina platensis in improvement of the reproductive performance and easing teratogenicity in hyperglycemic albino mice. Indian J Pharmacol [serial online] 2015 [cited 2023 Dec 5];47:430-5. Available from: https://www.ijp-online.com/text.asp?2015/47/4/430/161271

 » Introduction Top

Diabetes mellitus (DM) is a metabolic syndrome in which pancreatic β-cells fail to produce insulin resulting in hyperglycemia that affects many organs and contributes to several complications. [1] During pregnancy, DM can cause reproductive abnormalities, abortions, congenital anomalies, alterations of fetal growth, neonatal morbidity, and mortality. [2] Several epidemiological and experimental studies have confirmed that the likelihood of developing DM is higher among offspring of diabetic mothers. [3] DM is associated with functional and developmental disorientations of the reproductive system in laboratory animals.

Animal models have already been created using alloxan (AXN), a cytotoxic drug toward pancreatic β-cells to investigate the reproductive performance in diabetes and fetal development during pregnancy. [4] Female mice with AXN induced DM showed altered secretion of gonadotropins due to diminution in normal pituitary response as it hinders the hypothalamic-pituitary-gonadal axis. Various metabolites generated in diabetes such as ketone bodies and somatomedin inhibitors alter the embryonic development. [1]

Malformation is the earliest stages of organogenesis, corresponding to approximately the first 8 weeks of human gestation in DM. Virtually any organ system can be affected but the neural tube defect (NTD) and the heart diseases are most common. [5] Maternal DM (MDM) has been shown to increase reactive oxygen species (ROS) production initially in the yolk sac and inhibit free radicals scavenging molecules. [6] ROS intensify the incidence of DM associated developmental disorders in animal models during gestational period. Some plant nutrients containing antioxidants were found to ameliorate the functional and derived developmental disorder induced by DM. [7]

Spirulina platensis (SP) is a unicellular cyanobacterium belonging to cyanophyceae class, oscillatoriaceae family; this cyanobacterium is characterized by spiral chains of the cells enclosed in a thin sheath. It contains very potent naturally occurring antioxidant, free radical scavenging agents. [8] SP is nontoxic, bioavailable, and provide significant multiorgan protection against many drugs and chemicals induced toxic assaults. [9] Its active constituents exhibit anti-inflammatory, neuroprotective, hepatoprotective, immunomodulatory, and anticancer activities. [10]

To the best of our knowledge, there are no reports that describe effects of SP in diabetes associated developmental abnormalities such as alteration in implantation sites, viable embryos, gestation length. In the present study, it has been investigated about therapeutic effect of SP on functional and developmental aspects of mice that developed in hyperglycemia conditions in utero.

 » Materials and Methods Top

Plant Material

SP powder for all experiments was procured from Sunova Spirulina Ltd., Delhi, India. It was a spray dried product, standard in quality, and a part of bulk production by the industry.


Swiss Albino mice Mus musculus weighing 22-27 g were obtained from Central Drug Research Institute, Lucknow, India. Mice were maintained at the animal house of host University under standard conditions. Animals were fed with standard diet (Aashirwad Ltd., Chandigarh, India) and water ad libitum. Animals were maintained under controlled conditions (temperature [23 ± 1°C], humidity [50 ± 15%]), and normal photoperiod (12 h light-dark cycle). Eleven weeks old mice were acclimatized for 1-week prior to experimental studies. Rice husk was used as bedding material and changed daily. The research proposal (Reg. No. 5873/10) was approved by the Research Committee of the Department and all experimental procedures were performed in accordance with the guidelines of Institutional Animal Care Committee and the principles outlined in the Declaration of Helsinki.

Drugs and Chemicals

AXN-monohydrate was purchased from Spectrochem, India. All other chemicals and biochemical reagents were of analytical grade.

Induction of Diabetes

Animals were fasted for 16-18 h with free access of water prior to induction of diabetes. DM was induced by intra-peritoneal (i.p.) administration of AXN (450 mg kg−1 bw) in three injections at intervals of 48 h (150 mg kg−1 bw each time). Mice with blood glucose level above 200 mg/dl were considered as diabetic [11] and selected for further experimental investigations.

Experimental Design

The experimental mice were divided into four groups containing six mice in each group.

  • Group I: Control (normal saline, 10 ml/kg i.p.)
  • Group II: Diabetic control; diab (AXN 150 mg kg−1 bw for three times)
  • Group III: Diab + SP (diabetic control mice fed with 15 mg of SP)
  • Group IV: Ctrl + SP (control mice fed with 15 mg of SP).

Preparation and Administration of Spirulina Platensis Suspension

The suspension was prepared by supplementing 1.5 g of SP in 50 ml of distilled water. SP suspension was fed orally during entire tenure of experiment using infant feeding catheter (3 mm size) attached to a sterile syringe. Catheter was inserted into the gastric region of mice, and 0.5 ml of suspension containing of 15 mg of SP was discharged gradually into each test animals.

Determination of Fasting Blood Glucose Level

Fasting blood glucose level (FBGL) was determined using glucometer (Accu-Chek Active, Mumbai, India) and compatible blood glucose strips at different time points during the course of the study.

Estrous Cycle

The virgin female mice were divided into four groups, each containing 20 mice (n = 20). Vaginal smears were prepared and examined at regular time points during the duration of the study. Mice showing normal full cycle (4-5 days) were considered as normal. For the study of estrus cycle, vaginal smear of all the female mice were examined twice a day until the completion of the treatment by introducing 2-3 drops of physiological saline in vagina and final drop obtained in the dropper was examined microscopically.

Fertility Test

On 8 th day of post-DM induction, each female in estrus was placed in cage having one nondiabetic male mouse during the dark period of the cycle to allow overnight mating. Similar experimental setup was set up for other groups also. Next morning, male and female animals were separated, and vaginal smears were examined for the presence of sperms. The day when sperm was found in the vaginal smear was considered day 0 of gestation period and thereafter female mice were observed daily till delivery. Laparotomy was performed on day 8 of pregnancy to determine the implantation sites. Mice that did not deliver were anesthetized and sacrificed by decapitation. Uteri were removed and implantation sites, resorptions, and deformities were enumerated. [12]

Statistical Analysis

The statistical analysis of the data was done using SPSS. Data expressed as mean ± standard error of mean (SEM). Comparisons between two groups with normality and homogeneity of variances were performed by two-tailed unpaired Student's t-test. One-way analysis of variance (ANOVA) was used, followed by the post-hoc Tukey multiple comparison test to analyze data for control mice when the SP treated diabetic group was included. The levels of significance were set at P < 0.05 (almost significant) and P < 0.01 (significant).

 » Results Top

Effects of Spirulina Platensis Administration on Fasting Blood Glucose Level

FBGL of control animals ranged from 78.33 ± 3.88 to 83.02 ± 3.58 mg/dl during experimental period which later increased significantly (P < 0.01) to 273% at 21 days in diabetic mice [Figure 1]a. Decrease in the FBGL was observed when diabetic mice fed with SP (P < 0.01). FBGL decreased to 61% in diab + SP at 21 days. However, SP treated control mice showed an insignificant change in FBGL.
Figure 1: (a) Fasting blood glucose level (mg/dl). n = 10, data are presented as mean ± standard error of mean, (b) therapeutic effects of Spirulina platensis on estrous cycle phases of different groups of test mice. n = 20, values are expressed as mean ± standard error of mean; superscripts ** are significantly different at P < 0.01 when compared to control. One-way analysis of variance was used followed by the post-hoc Tukey multiple comparison test

Click here to view

Estrous Cycle Phases of Different Groups of Mice

Control animals showed 11 ± 0.89 h for estrus phase, 10 ± 0.89 h for metestrus phase, 65 ± 0.89 h for diestrus phase and 103.5 ± 2.74 h for total period of cycle which were increased by 91%, 180%, 15.38%, and 32.36%, respectively in diabetic mice when compared with control [Figure 1]b. A significant decrease (P < 0.05) was witnessed in proestrus phase (74.28%) of diabetic when compared to control. Control mice when fed with SP showed insignificant change in proestrus phase.

Litters Count, Implantation Sites and Gestation Length of Test Groups of Mice

Control animals showed 11.00 ± 0.63 implantation sites and 10.43 ± 0.75 l count per animal. The numbers of implanted embryos were decreased to 22.72% in diabetic whereas SP treatment increased the value to 11.76% [Figure 2]. Gestation length of control mice was found to 19.50 ± 0.55 days that were increased to 14.51% days in diabetic (P < 0.01) following treatment with SP, gestation length decreased nearly to normal.
Figure 2: Therapeutic potential of Spirulina platensis in modulating fertilities and preweaning development studies of different groups of mice. (a) Effects on litters counts, implantation sites and gestation length of test groups of mice. Data are presented as mean ± standard error of the mean of 40 animals. **P < 0.01 when the value are compared with Group I. One-way analysis of variance was used followed by the post-hoc Tukey multiple comparison test. (b) Preweaning development in test groups of mice. Data are expressed as mean ± standard error of mean of 20 mice

Click here to view

Preweaning Development of Test Groups of Mice

Diabetic mice with defective forelimb and hind limb including digits [Figure 3]a and b, puffiness of the body and venations in the ear [Figure 3]c and d, retinopathy with altered gross morphology [Figure 3]e and f, pattern baldness (alopecia) in F 1 mice [Figure 3]g, deformed fetus [Figure 3]h-k, and fetus with abnormal length and weight during 18 days of gestation length were observed [Figure 3]l.
Figure 3: Gross morphological deformity and disturbed fetal development. (a and b) Diabetic mice with defective forelimb and hind limb including digits, (c and d) puffiness of the body and venations in the ear (dorsal and ventral view), (e and f) retinopathy with altered gross morphology, (g) pattern baldness (alopecia) in F1 mice, (h and k) deformed fetus, (l) fetus with abnormal length and weight of 18 days gestation length

Click here to view

Litters in Fertilities Studies

Control animals (n = 40) showed 10.43 ± 0.32 implantation site as compared to diabetic that possessed 6.58 ± 0.24 implantation site per animal. When mice were fed with SP at fixed dose (15 mg kg−1 bw d−1 ), implantation sites were found to be 7.83 ± 0.22 which corresponds to 37% increase compared to diab. Percentage implantational loss was highest in diabetic control (58.9%) which was reduced to 21% in diab + SP. Live pups at birth in diabetic mice were decreased to 83.51% on the other hand, number of dead fetus of 0 day age increased to 40% in MDM group when compared to normal mice. Resorption rate (36.14%) and abnormal fetus (66.67%) were increased in diab when compared to ctrl [Table 1].
Table 1: Effects of Spirulina platensis on reproduction performance and survival rate of F1 progeny of test group of mice

Click here to view

F0 Generations During Fertilities Studies

Mice (n = 40) of F 0 generation were employed for fertilities studies. Reproductive performance was shown by 36 control animals that decreased to 31 in diabetic mice out of 40. Feeding of diabetic mice with SP increased their numbers to 33. Fertilities rate were observed minimum (77.5%) in diabetic group, and these were increased to 82.5% in diab + SP. Death during delivery was higher (3.23%) in diabetic mice as compared to control that showed no mortality. Mortality rate was also decreased from 4 to 3 as a result of administration of SP to diabetic mice [Table 2].
Table 2: Effects of Spirulina platensis on fertilities of F0 mice and death of F1 progeny of test group of mice

Click here to view

 » Discussion Top

AXN induced hyperglycemia is considered as valid experimental model to study the reproductive performance in diabetic mice. AXN selectively obliterated the pancreatic insulin secreting β-cells, leaving less active cells, and resulting in a diabetic state. Some β-cells of  Islets of Langerhans More Details remained active thus helping to survive in spite of increasing FBGL.

The reproductive toxicity was assessed based on an array of parameters such as estrus cycle stages (proestrus, estrus, metestrus, and diestrus) of various duration, implantation sites, implantational loss, fertilities studies, live pregnant at delivery, live pups at birth, survival rate (0-4 days), gestation length, and preweaning development. Cyclic changes were observed in the estrous cycle, gave a reasonable index of the ovarian activity and synthesis of estrogen and progesterone. The control mice exhibited regular and normal duration of each phases of estrous cycle. In contrast, diabetic mice exhibited significant increase in the length of estrous cycle, duration of estrus, diestrus and metestrus with concomitant decrease in the duration of proestrus phase (P < 0.01) which were further regained by SP supplementation. The appearance of prolonged diestrus indicates secretion of estrogen from ovary must be affected. It might be due to less secretion of gonadotropins, thus causing hormonal imbalances.

Similar results had been reported when mice treated with a carbamate fungicide mancozeb, [13] cyclophosphamide. [14] Similar findings like increased BGL and decreased insulin level were also noted in test mice. Such biochemical changes act on the hypothalamus that affects the ovary that in turn alter estrous cycle and folliculogenesis. [15] The number of implantation sites was significantly (P < 0.01) reduced by progression of hyperglycemic state. This condition was however ameliorated by SP supplementation [Figure 4].
Figure 4: Graphical summary

Click here to view

Diabetic mice have shown an increased BGL from day 1 onward and continued until the end of the experiment. Similarly, induction of diabetes using AXN leading to hyperglycemic condition have been reported by a number of researchers. [10],[16] The results on the decreased FBGL were indicative of the curative effect of SP in induced diabetic mice models. Treatment with SP for 21 days resulted in utmost reversal of the hyperglycemic condition in diabetic mice. In this regard, SP has already been established for its hypoglycemic effect in human subjects. [8],[17]

SP contains satisfactory amount of trace metal mixtures (chromium, magnesium, manganese, and zinc) which improve glucose tolerance by assisting glucose transport and regulation of glucose homeostasis. Dietary fibers present in SP help in improving blood sugar level by slowing down the absorption of sugar. [18]

In one of the study, embryos of mice when injected with glucose caused NTD. [5] In a diabetic condition, a high proportion of glucose is metabolized through the polyol pathway, where aldose reductase reduces glucose to sorbitol. Sorbitol may accumulate in tissue and cause damage through osmotic effects. The increased availability of glucose in experimental diabetic pregnancy is paralleled by an increase in embryonic sorbitol concentration. MDM caused an increase in both sorbitol content and aldose reductase activity in fetus. [19]

ROS reacts with lipids causing altered cell membrane fluidity. [20] These mechanisms have been suggested to be part of the pathogenesis of diabetic embryopathy. MDM is associated with increased oxidative stress (OS) in the embryo during organogenesis and induced malformations. [15],[16]

The beneficial effect of giving Vitamin C and E to the pregnant diabetic mice in the management of diabetic embryopathy have already been established. [21],[22],[23],[24] Orally fed natural antioxidant-Vitamin C (100 mg kg−1 bw for 15 days) showed 49.14% reduction of FBGL in AXN diabetic rat. [21] Similarly, diabetic rat when fed with dietary antioxidant (0.5% Vitamin C and 0.5% Vitamin E supplemented diet for 10 days) did not lower down the FBGL to the steady levels but there was significant reduction (P < 0.05) as compared to DM group. FBGL reduced up to the mark when the double concentration of Vitamin C keeping Vitamin E as usual was given. [22]

Thirty percentage increase in placental weight was observed in MDM, but supplementation of 1% Vitamin C and 0.5% Vitamin E with food restored the placental weight by approximately 35% in 20 days gestational diabetic rats. In the MDM groups, 23% malformations and 32% resorptions were observed which were successively decreased by Vitamin C treatment. [23] Results were in agreement with other workers who suggested that Vitamin C may prevent the accumulation of sorbitol intracellularly by inhibiting the aldose reductase enzyme and maintaining glucose homeostasis. [24] SP contains antioxidant (Vitamin C and E) and blood sugar lowering agents whose treatment resulted in an improvement of pregnancy outcome, manifested as decreased rates of malformations and resorptions in the treated group of mice. [18]

In relation to physical development, the time taken for ear unfolding, upper incisor development, and eye opening was observed among new born and found to be insignificant. Some worker reported delay in the duration of development as well as neonatal growth that might be related to intrauterine disturbances during pregnancy caused by MDM. [25]

Medicinal plants/plant extracts containing secondary metabolites like phenolic compounds, alkaloids, flavonoids, saponins, terpenoids, and phytosterol were found to be effective in the management of diabetic complications. [26] In this regard, Tinospora cordifolia and Ipomoea aquatica (whole leaf powder) were investigated to attenuate embryopathy, OS and protection in the fetal brain and liver, as evidenced by increased levels of antioxidant molecules and reductions of ROS in streptozotocin-diabetic rats. [27]

The placenta represents an important line of defense against any embryopathic agent within the feto-maternal unit. Both human and animal studies have confirmed that phytonutrients can easily cross the placental barrier. [27] The teratological part of the present experiment showed a prominent reduction in the malformations rate and resorptions rate after treatment. However, SP administration remarkably reduced the hyperglycemia-generated detrimental tendencies. On the other hand, SP preserved the significant number of fetuses after having raised the number of implantations, probably referring to the antioxidant activity, thus allowing preparing a proper local environment that supports postimplantational development. In contrast to the identified external anomalies in ctrl and diab + SP, no skeletal dysmorphia were seen in these groups, suggesting that chronic hyperglycemia is directly involved in skeleton mal-development. In this context, progeny from diabetic animals are frequently subjected to paralysis of limb, puffiness of the body, venations in the ear, alopecia, retinopathy, altered gross morphology, and deformity in the fetus.

From this study, it can be concluded that oral therapeutic treatment with SP suspension to pregnant diabetic mice modulates reproductive performance, alleviate maternal hyperglycemic state and attenuate diabetic teratogenesis. Results clearly unmasked therapeutic effects of SP against diabetic embryopathies and warrants further investigation at wider dose regimens in other test animals.

 » Acknowledgment Top

The author gratefully acknowledges the financial assistance from UGC, New Delhi (F.17-126/98 [SA-I]; 06/10/2008) and thank to Head and staff members of University Department of Zoology, TM Bhagalpur University, Bhagalpur, Bihar for their support in providing research facilities.

Financial Support and Sponsorship

UGC, New Delhi, India; (F.17-126/98 [SA-I]; 06/10/2008).

Conflicts of Interest

There are no conflicts of interest.

 » References Top

Olokoba AB, Obateru OA, Olokoba LB. Type 2 diabetes mellitus: A review of current trends. Oman Med J 2012;27:269-73.  Back to cited text no. 1
Wong VW, Suwandarathne H, Russell H. Women with pre-existing diabetes under the care of diabetes specialist prior to pregnancy: Are their outcomes better? Aust N Z J Obstet Gynaecol 2013;53:207-10.  Back to cited text no. 2
Kuo CC, Moon K, Thayer KA, Navas-Acien A. Environmental chemicals and type 2 diabetes: An updated systematic review of the epidemiologic evidence. Curr Diab Rep 2013;13:831-49.  Back to cited text no. 3
King AJ. The use of animal models in diabetes research. Br J Pharmacol 2012;166:877-94.  Back to cited text no. 4
Kappen C, Kruger C, MacGowan J, Salbaum JM. Maternal diet modulates the risk for neural tube defects in a mouse model of diabetic pregnancy. Reprod Toxicol 2011;31:41-9.  Back to cited text no. 5
Xin G, DU J, Wang YT, Liang TT. Effect of oxidative stress on heme oxygenase-1 expression in patients with gestational diabetes mellitus. Exp Ther Med 2014;7:478-82.  Back to cited text no. 6
Dada OK, Akindele AJ, Morakinyo OA, Sofidiya MO, Ota D. Hypoglycemic and antioxidant activities of the hydroethanolic leaf extract of Byrsocarpus coccineus Schumach. and Thonn. (Connaraceae). Chin J Nat Med 2013;11:628-37.  Back to cited text no. 7
Hosseini SM, Khosravi-Darani K, Mozafari MR. Nutritional and medical applications of Spirulina microalgae. Mini Rev Med Chem 2013;13:1231-7.  Back to cited text no. 8
Abdel-Daim MM, Abuzead SM, Halawa SM. Protective role of Spirulina platensis against acute deltamethrin-induced toxicity in rats. PLoS One 2013;8:e72991.  Back to cited text no. 9
Deng R, Chow TJ. Hypolipidemic, antioxidant, and antiinflammatory activities of microalgae Spirulina. Cardiovasc Ther 2010;28:e33-45.  Back to cited text no. 10
Lenzen S. The mechanisms of alloxan- and streptozotocin-induced diabetes. Diabetologia 2008;51:216-26.  Back to cited text no. 11
Leung MB, Choy KW, Copp AJ, Pang CP, Shum AS. Hyperglycaemia potentiates the teratogenicity of retinoic acid in diabetic pregnancy in mice. Diabetologia 2004;47:515-22.  Back to cited text no. 12
Mahadevaswami MP, Jadaramkunti UC, Hiremath MB, Kaliwal BB. Effect of mancozeb on ovarian compensatory hypertrophy and biochemical constituents in hemicastrated albino rat. Reprod Toxicol 2000;14:127-34.  Back to cited text no. 13
Kishk EA, Mohammed Ali MH. Effect of a gonadotropin-releasing hormone analogue on cyclophosphamide-induced ovarian toxicity in adult mice. Arch Gynecol Obstet 2013;287:1023-9.  Back to cited text no. 14
Hirshfeld-Cytron JE, Duncan FE, Xu M, Jozefik JK, Shea LD, Woodruff TK. Animal age, weight and estrus cycle stage impact the quality of in vitro grown follicles. Hum Reprod 2011;26:2473-85.  Back to cited text no. 15
Sharma R, Kumar V, Ashok BK, Galib R, Prajapati PK, Ravishankar B. Hypoglycemic and anti-hyperglycemic activity of Guduchi Satva in experimental animals. Ayu 2013;34:417-20.  Back to cited text no. 16
[PUBMED]  Medknow Journal  
Karkos PD, Leong SC, Karkos CD, Sivaji N, Assimakopoulos DA. Spirulina in clinical practice: Evidence-based human applications. Evid Based Complement Alternat Med 2011;2011:531053.  Back to cited text no. 17
Pankaj PP, Varma MC. Potential role of Spirulina platensis in retaining altered blood parameters in alloxan induced diabetic mice. Int J Pharm Pharm Sci 2013;5:450-6.  Back to cited text no. 18
Zhao Z, Reece EA. New concepts in diabetic embryopathy. Clin Lab Med 2013;33:207-33.  Back to cited text no. 19
Afanas′ev I. Signaling of reactive oxygen and nitrogen species in diabetes mellitus. Oxid Med Cell Longev 2010;3:361-73.  Back to cited text no. 20
Simán CM, Eriksson UJ. Vitamin C supplementation of the maternal diet reduces the rate of malformation in the offspring of diabetic rats. Diabetologia 1997;40:1416-24.  Back to cited text no. 21
Garg MC, Bansal DD. Protective antioxidant effect of Vitamins C and E in streptozotocin induced diabetic rats. Indian J Exp Biol 2000;38:101-4.  Back to cited text no. 22
Cederberg J, Simán CM, Eriksson UJ. Combined treatment with Vitamin E and Vitamin C decreases oxidative stress and improves fetal outcome in experimental diabetic pregnancy. Pediatr Res 2001;49:755-62.  Back to cited text no. 23
Þimþek M, Nazýroğlu M, Erdinc A. Moderate exercise with a dietary Vitamin C and E combination protects against streptozotocin-induced oxidative damage to the kidney and lens in pregnant rats. Exp Clin Endocrinol Diabetes 2005;113:53-9.  Back to cited text no. 24
Ge ZJ, Liang QX, Luo SM, Wei YC, Han ZM, Schatten H, et al. Diabetic uterus environment may play a key role in alterations of DNA methylation of several imprinted genes at mid-gestation in mice. Reprod Biol Endocrinol 2013;11:119.  Back to cited text no. 25
Singh R, Kaur N, Kishore L, Gupta GK. Management of diabetic complications: A chemical constituents based approach. J Ethnopharmacol 2013;150:51-70.  Back to cited text no. 26
Shivananjappa MM, Muralidhara. Dietary supplementation with Ipomoea aquatica (whole leaf powder) attenuates maternal and fetal oxidative stress in streptozotocin-diabetic rats. J Diabetes 2013;5:25-33.  Back to cited text no. 27


  [Figure 1], [Figure 2], [Figure 3], [Figure 4]

  [Table 1], [Table 2]

This article has been cited by
1 Oral Administration of Spirulina platensis at Early Gestation Modulates Litter Size and the Expression of Inhibin, Insulin, IGF-I, CO Q10, and BMP-15 in Ewes Induced for Twinning
Moustafa Zeitoun, Mohamed Ali, Tariq Almundarij, Emad Mousa, Ahmed Alghonaim, Juan Pablo Damián
Veterinary Medicine International. 2023; 2023: 1
[Pubmed] | [DOI]
2 An Overview of Pharmacological and Clinical Aspects of Spirulina
Ramin Ansari, Farzaneh Foroughinia, Amir Hossein Dadbakhsh, Forough Afsari, Mohammad Mehdi Zarshenas
Current Drug Discovery Technologies. 2023; 20(2)
[Pubmed] | [DOI]
3 Polymethoxy-1-Alkenes Screening of Chlorella and Spirulina Food Supplements Coupled with In Vivo Toxicity Studies
Eliana Henao, Patrick J. Murphy, Halina Falfushynska, Oksana Horyn, Daniel M. Evans, Piotr Klimaszyk, Piotr Rzymski
Toxins. 2020; 12(2): 111
[Pubmed] | [DOI]
4 Effects of Spirulina platensis on insulin secretion, dipeptidyl peptidase IV activity and both carbohydrate digestion and absorption indicate potential as an adjunctive therapy for diabetes
J. M. A. Hannan, Prawej Ansari, Shofiul Azam, Peter R. Flatt, Yasser H. A. Abdel Wahab
British Journal of Nutrition. 2020; 124(10): 1021
[Pubmed] | [DOI]


Print this article  Email this article


Site Map | Home | Contact Us | Feedback | Copyright and Disclaimer | Privacy Notice
Online since 20th July '04
Published by Wolters Kluwer - Medknow