- Research article
- Open Access
- Open Peer Review
Chlorophytum borivilianum (Safed Musli) root extract prevents impairment in characteristics and elevation of oxidative stress in sperm of streptozotocin-induced adult male diabetic Wistar rats
© Giribabu et al.; licensee BioMed Central Ltd. 2014
- Received: 14 March 2014
- Accepted: 23 July 2014
- Published: 8 August 2014
We hypothesized that C. borivilianum root, known to improve male reproductive performance, prevents impairment in characteristics, morphology and elevation of oxidative stress in sperm of diabetics. We therefore investigated the effect of aqueous root extract of C. borivilianum on these parameters in diabetic rat model.
C. borivilianum root aqueous extract (250 and 500 mg/kg/day) or glibenclamide (600 μg/kg/day) were administered to streptozotocin (STZ)-induced diabetic male rats for 28 consecutive days. At the end of treatment, animals were sacrificed and sperm were collected. Sperm count and percentages of forward motility, viability, hypoosmotic swelling (HOS) tail-coiled and abnormal sperm were evaluated. Sperm lipid peroxidation product (LPO), hydrogen peroxide (H2O2) and nitric oxide (NO) levels, total antioxidant capacity (TAC), activity levels of endogenous antioxidant enzymes (superoxide dismutase-SOD, catalase-CAT and glutathione peroxidase-GPx), epididymal sperm density, serum fasting blood glucose (FBG) and HbA1c levels were measured. The expression of sperm caspase-3 was assessed. Meanwhile, in-vitro free radical scavenging activity of C. borivilianum root extract was determined and the root extract was analyzed for the presence of bioactive compounds by FTIR spectroscopy.
C. borivilianum root aqueous extract prevents the decrease in sperm count, percentages of forward motility, viability, HOS and the increase in abnormal sperm percentage and caspase-3 level in diabetic rats. Sperm LPO, H2O2 and NO levels, FBG and HbA1c were lower while TAC, SOD, CAT, GPx and epididymal sperm density were higher in diabetic rats receiving C. borivilianum root extract treatment. C. borivilianum root exhibited strong in-vitro free radical scavenging activity which may be due to the phenolic compound.
C. borivilianum root extract prevents impairment in sperm characteristics and morphology via preventing elevation of oxidative stress, apoptosis and free radicals levels of the sperm in diabetes. These effects may be achieved through maintaining sperm antioxidant level which could be related to free radical scavenging activity of the root extract by phenolic compounds. These effects could also be due to ability of the extract to maintain near normal serum FBG and HBA1c levels in diabetes.
- C. borivilianum
- Diabetes mellitus
- Oxidative stress
Diabetes mellitus (DM), characterized by chronic hyperglycemia resulting from deficiency of insulin secretion, resistance to insulin action or both, is associated with long-term damage, dysfunction and failure of various organs . An alarming high rate of infertility has been reported in diabetic male . Diabetes was found to adversely affect the sperm. Rama Raju et al.,  reported that diabetic men have high percentage of sperm nuclear DNA fragmentation and apoptosis. Meanwhile, Thakur et al.,  reported that hyperglycemia in rats diminished sperm count, seminal fluid fructose and antioxidant enzymes. A recent study by Battacharya et al.,  reported that husbands of infertile couples with diabetes possess lower volume of ejaculates, sperm count and percentage of motile sperm as compared to healthy husbands of couples with proven fertility.
Safed Musli or Chlorophytum borivilianum (family: Lilliaceae) is a highly valued medicinal plant in India and is considered as “white gold” in Indian system of Ayurveda . This plant has been reported to possess a number of biological activities including antimicrobial, anti-inflammatory, antipyretic, hepatoprotective, antioxidant, hypolipidemic and antidiabetic . Traditionally, C. borivilianum root has been used to treat male impotence, oligozoospermia and erectile dysfunction . Kenjale et al.,  reported that oral administration of 250 mg/kg/day of C. borivilianum root aqueous extract to normal, healthy male rats preserved sperm count while Thakur et al.,  reported that oral administration of 200 mg/kg/day of this plant extract to adult hyperglycemic male rats provides protection against sexual dysfunction as indicated by high frequency mounting, intromission and ejaculation.
Oxidative stress-induced sperm damage has been suggested as an important pathological mechanism underlying male infertility . The sperm plasma membrane is susceptible to oxidation due to high content of polyunsaturated fatty acids (PUFA) . Lipid peroxidation in sperm membrane can cause various impairments including decreased sperm motility . The sperm could be protected from oxidative damage by endogenous antioxidant enzymes which are found both in sperm  and seminal fluid . Meanwhile, the decrease in seminal fluid antioxidant level was reported to contribute to male infertility in humans .
We hypothesized that C. borivilianum root prevents impairment in sperm characteristics and morphology, oxidative stress and apoptosis in diabetic rats. This study therefore aimed to investigate C. borivilianum root extract effect on these sperm parameters in diabetes and to extent the previous observations in normal male rats whereby oral administration of this plant root extract improved male reproductive capability [9, 10].
Drugs and chemicals
Streptozotocin was purchased from Sigma Aldrich (St. Louis, MO, USA). All other chemicals used were of analytical grade.
Plant collection and preparation of plant extract
Dried roots of C. borivilianum were procured from Nandan Agro Farms Pvt. Ltd. (Hyderabad, Andhra Pradesh, India) and authenticated by senior botanist, Madhava Setty, Sri Venkateswara University, Tirupati, India. The plant was deposited at Herbarium with the number: KLU 96568. The dried roots were cut into small pieces and grounded into fine powder. The root powder (1000 g) was subjected to cold maceration in 2 L of sterile distilled water for 48 hours at room temperature, filtered into a clean round bottom flask using adsorbent cotton wool and a filter paper (Whatman No. A-1). The whole process was repeated seven times to ensure maximum yield of water soluble compounds from the root powder. The combined aqueous extract was concentrated at 37°C using a rotary evaporator (R-210, Buchi Labortechnik AG, Flawil, Switzerland) and lyophilized by using a cyodos freeze dryer (Telstar, Barcelona, Spain) to yield approximately 38 g of solid extract (3.8% w/w).
A qualitative phytochemical evaluation was performed on the aqueous root extracts to determine the presence of carbohydrates (Barfoed’s test), flavonoids (test of Shinoda), phytosterols (Libermann Buchard test), phenols (ferric chloride test), alkaloids (Dragendorff test), proteins (Biuret test) and saponins (Saponification test) following the methods as described by Harbourne .
Fourier transform infrared (FTIR) spectroscopy
FTIR spectroscopic analysis was performed using Perkin Elmer spectrophotometer system (PerkinElmer, Inc., Shelton, CT, USA) which detects the characteristic peaks and functional groups that are present in the root extract. The spectral range 4000 to 600 cm-1 with resolution of 2 cm-1 was used to record the infrared spectra with the potassium bromide (KBr) pellet making technique.
Adult male Wistar rats (170–200 g) were obtained from Animal House, Faculty of Medicine, University of Malaya (UM). The rats were kept under standard environmental conditions of room temperature 25 ± 2°C, relative humidity between 45-55% and 12 hrs light/dark cycle. Animals were fed with standard feed pellets (Harlan diet, UK) and tap water ad libitum. Experimental procedures were in accordance with ARRIVE guidelines (Animals in Research: Reporting In-Vivo Experiments) and European Community Guidelines/ EEC Directive, 1986. This study was approved by the Faculty of Medicine, Animal Care and Use Committee (ACUC), University of Malaya with ethics number: 2013-07-15/FIS/R/NS. Toxicity study was conducted according to Organization for Economic Cooperation and Development (OECD) revised up-and-down procedure for acute toxicity testing (OECD guideline 425) . No signs of toxicity were observed in the tested animals up to a dose of 3000 mg/kg/day.
Induction of diabetes
Hyperglycemia was induced in overnight fasted male rats by a single intraperitoneal injection of STZ dissolved in ice cold citrate buffer (0.1 M, pH 4.5) at a dose of 55 mg/kg . The rats were allowed to drink 5% sucrose solution overnight after injection, to overcome drug-induced hypoglycemia. Diabetes was confirmed by the presence of polydipsia, polyuria and weight loss and only animals exhibiting a fasting glucose level greater than 300 mg/dL three days after STZ injection were used in this study. Treatment with C. borivilianum was commenced four days after STZ injection and this was considered as day one. C. borivilianum root extract at 250 and 500 mg/kg/day  were administered in the form of suspension in 1% sodium carboxymethylcellulose (Na-CMC) dissolved in distilled water daily for 28 consecutive days using an oral gavage tube.
The animals were randomly assigned into five experimental groups with six (6) rats per group:
Group I - Control rats- received 1% Na-CMC vehicle only.
Group II - Diabetic control rats- received 1% Na-CMC vehicle only.
Group III and IV - Diabetic rats treated with C. borivilianum root aqueous extract at 250 & 500 mg/kg body weight respectively.
Group V- Diabetic rats treated with standard antidiabetic agent, glibenclamide at 600 μg/kg body weight.
At the end of experimental period, all rats were fasted overnight, weighted and sacrificed under pentobarbital sodium anesthesia (60 mg/kg) followed by cervical dislocation.
Determination of sperm characteristics and morphology
Immediately after euthanasia, cauda epididymis were dissected out, chopped and placed in 5 ml physiological saline (0.9% NaCl) and incubated for 5 min at 37°C in water bath to allow sperm to leave the epididymal tubules.
Evaluation of sperm forward motility
Progressive sperm motility was evaluated by a method of Belsey et al. . Firstly, immotile sperm were counted followed by motile sperm. Sperm forward motility was expressed as percentage of motile sperm to total sperm counted.
Sperm count was determined using Neubauer chamber (Deep 1/10 mm, LAMBART, Darmstadt, Germany) of hemocytometer following the method as described by Belsey et al. . Sperm count was expressed as number of sperm per ml of solution.
The ratio of live to dead sperm was determined using 1% trypan blue staining following the method as described by Talbot and Chacon . A total number of 200 sperm were counted per slide and the results were expressed as percentage of the live sperm.
Hypo-osmotic Swelling Test (HOST)
Sperm’s flagella membrane integrity was assessed by hypo-osmotic swelling test (HOST). In brief, assay was performed by incubating 50 μL sperm suspension with 1 mL hypo-osmotic solution. Two hundred sperm were evaluated and percentage of live sperm (with coiled tail) was calculated following the method of Jeyendran et al. .
Sperm morphological abnormalities
Percentages of sperm head, middle piece and tail abnormalities were determined from a total of 300 sperm per rat . Sperm morphology was viewed under a light microscope (Nikon, H600L, Tokyo, Japan) under 400 × magnifications. Data was expressed as percentage of morphologically abnormal sperm to total sperm count.
Following analysis of sperm parameters, the remaining cauda epididymal sperm suspension was centrifuged at 800 g for 20 min at 4°C and the pellet was resuspended in normal saline. The sperm were homogenized with a glass-Teflon Homogenizer (Heidolph Silent Crusher M, Germany). The supernatant collected was used for biochemical studies.
Assessment of sperm lipid peroxidation
The lipid peroxidation level in sperm homogenate was measured as malondialdehyde (MDA), which is the end product of lipid peroxidation, which reacts with thiobarbituric acid (TBA) to produce TBA reactive substance (TBARS), a red colored complex which has peak absorbance at 532 nm, according to the method of Ohkawa et al., .
Determination of Hydrogen peroxide and nitric oxide level in sperm
In the supernatant levels of H2O2 were estimated according to the method by Pick . In brief, H2O2 mediates horseradish peroxidase-dependent oxidation of phenol red and the results obtained were expressed as nmol H2O2 formed g-1 tissue. Nitric oxide (NO) concentration was measured as nitrite/nitrate by previous method of Miranda et al., . The NO levels were expressed as nmol/g tissue.
Assessment of Sperm Total Antioxidant Capacity (TAC)
The total antioxidant capacity of sperm homogenate was measured according to the modified method of Erel, , where the samples were mixed with acetate buffer, and 2,2’-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS reagent) with hydrogen peroxide. The color reaction was monitored spectrophotometrically at 660 nm. The results were expressed as μmolequivalents Trolox/mg protein.
Determination of sperm endogenous antioxidant enzyme activity
SOD activity level was assayed according to the method by Misra and Fridovich  and was expressed as the amount of enzyme that inhibits oxidation of epinephrine by 50%, which was equal to 1U per milligram of protein. CAT activity level was determined on the basis of H2O2 decomposition  and was expressed in μmol of H2O2 metabolized/mg protein/min. Meanwhile, GPx activity level was determined according to the method by Rotruck et al.  and was expressed as μmol of GSH consumed/mg protein/min.
In-vitro radical scavenging activity of C. borivilianum root extract
Ao = absorbance of control group (without plant extract) and At = absorbance of C. borivilianum root aqueous extract. Absorbance was measured using a spectrophotometer (UV-1700, Shimadzu, Kyoto, Japan) at different wavelengths depending on the type of assay performed. All assays were carried out in triplicate.
Radical-scavenging activity of C. borivilianum root aqueous extract against stable DPPH radical was determined according to the method by Katalinic et al., . Measurement of superoxide radical scavenging activity was based on the method by Xiang and Ning . Hydroxyl radical scavenging activity was measured using a modified method by Halliwell et al., . The ability of C. borivilianum root aqueous extract to scavenge H2O2 was determined according to the method by Ruch et al., . The ability of the extract to scavenge nitric oxide was determined using a method by Dastmalchi et al., . Finally, reducing power scavenging activity of C. borivilianum root extract was determined according to the method by Suseela et al., .
Estimation of sperm caspase-3 levels
Snapped-frozen sperm were homogenized using a sonicator with PRO-PREP (iNtRON Biotechnology, Seoul, South Korea) extraction solution in the presence of protease inhibitors. Total cell protein was obtained by centrifugation at 13000 g for 15 minutes at 4°C. After determination of the protein concentration, the same amount of protein was loaded into the 12% SDS-PAGE gel. The protein was then transferred onto the polyvinyilidene difluoride (PVDF) membrane and incubated in 5% BSA for 90 minutes. The blot was then exposed to primary antibody, caspase-3 rabbit polyclonal IgG, Santa Cruz, USA (sc-7148) at 1:1000 dilution. Following primary antibody incubation, the blot was incubated with HRP-conjugated secondary antibody and finally visualized by using Optic 4C (Bio RAD). β-actin (Santa cruz, sc-130656) was used as a loading control. Photos of the blots were captured and density of each band was determined using Image J software (1.39, Bethesda, Maryland, USA). The ratio of caspase-3/ β-actin band density was determined and was considered the expression level of each of the target proteins.
Determination of Serum HbA1c and Fasting Blood Glucose (FBG) Levels
At the end of 28 day treatment, blood was withdrawn from retro-orbital plexus in overnight fasted diabetic rats. Glucose levels were estimated using glucose oxidase/peroxidase kit (BioSystems S.A. Costa Brava 30, Barcelona, Spain) and HbA1c was measured using a commercially available kit (BioSystems S.A. Costa Brava 30, Barcelona, Spain). The values were estimated using an automated analyzer Dimension RxL Max Integrated Chemistry System (Siemens Healthcare Diagnostics Inc. Deerfield, IL, USA).
Epididymal sperm density
Caput epididymis was freshly harvested and fixed in 10% formaldehyde for 24 hours. The tissue was dehydrated in ethanol, cleared in xylene and embedded in paraffin at 58°C. The embedded tissue samples were cut into 5 μm thickness using a microtome (Histo-line laboratories, ARM-3600, Viabrembo, Milano, Italy). After deparaffinization by immersion into xylene for 20 min, tissues were dropped in ethanol solution of decreasing concentrations (100%, 95%, 90% and 80%) for 5 min. Sections were then stained with hematoxylin and eosin (H&E). Sperm density in epididymal lumen was graded as normal (+++), moderately decreased (++), or severely decreased (+) according to description by Narayana et al., .
Statistical differences were evaluated by analysis of variance (ANOVA) and Student’s t-test. A probability level of less than 0.05 (p < 0.05) was considered as significant. Post-hoc statistical power analysis was performed for all the experiments and values > 0.8 were considered as adequate. Meanwhile, Shapiro-Wilk test was performed to test for data normality and values > 0.05 indicated that data were normally distributed.
Qualitative phytochemical screening of aqueous extract of C. borivilianum root showed the presence of carbohydrates, proteins, phytosterols and saponins (data not shown).
FTIR spectral analysis
FTIR peak values of extracts of C. borivilianum root extract
Name of the group
3385.62 cm-1 (broad trough )
OH (Alcohol) /Phenol
Alcohol/Phenol (High concentration)
2929.67 cm-1 (medium-strong )
CH2 = CH-
1722.13 cm-1 (weak band)
(May be 80%)
Saturated aliphatic/cyclic 6-membered
C = C (Aromatic ring)
Aromatic C = C bond
Aromatic ether linkage (-O-Aromatic ring)
Aromatic ether linkage (phenol derivative)
1151 cm-1 (weak band)
Alcohol (secondary alcohol)
1028 cm-1 (strong band)
Aromatic ether stretching frequency
Aromatic ether linkage
Mono substituted benzene
Mono substituted aromatic ring
Effect on sperm characteristics
Effect of C. borivilianum root extract on sperm parameters
250 mg/kg C. borivilianum
500 mg/kg C. borivilianum
600 μg/kg glibenclamide
Sperm count (millions/ml)
78.64 ± 6.74
45.87* ± 6.87
61.68† ± 5.86
68.64† ± 5.68
69.52† ± 5.71
Sperm motility (%)
73.76 ± 5.84
43.68* ± 6.79
58.75† ± 4.38
68.47† ± 5.76
69.68† ± 5.61
Sperm viability (%)
82.69 ± 4.47
62.87* ± 3.86
71.34† ± 4.79
73.35† ± 4.08
75.38† ± 5.35
HOS tail coiled sperm (%)
69.58 ± 3.64
43.27* ± 3.78
54.86† ± 4.37
61.78† ± 3.61
62.42† ± 4.13
Meanwhile, sperm motility in diabetic rats was 40.78% lower than normal non-diabetic rats. 28-days treatment with C. borivilianum root extract resulted in a significantly higher progressive sperm motility (34.50% and 56.75% respectively) as compared to non-treated diabetic rats. Treatment with 600 μg/kg/day glibenclamide resulted in 59.52% higher progressive sperm motility as compared to non-treated diabetic rats. Glibenclamide was 1.73 times more potent than 250 mg/kg/day C. borivilianum root extract in causing an increase in sperm progressive (forward) motility in diabetic rats.
The sperm viability was 23.97% lower in diabetic rats than normal, non-diabetic rats. 28-days treatment with C. borivilianum root extract resulted in a significantly higher viability (13.47 and 16.67% respectively) as compared to non-treated diabetic rats. Meanwhile, treatment with glibenclamide resulted in 19.9% higher viability as compared to non-treated diabetic rats. Glibenclamide treatment was 1.48 times more potent than 250 mg/kg/day C. borivilianum root extract in causing increased in sperm viability in diabetic rats.
The HOS tail coiled sperm was 37.82% lower in diabetic rats than normal, non-diabetic rats. 28-days treatment with 250 and 500 mg/kg/day C. borivilianum root extracts resulted in 26.79% and 42.87% higher HOS tail-coiled sperm respectively as compared to non-treated diabetic rats. Treatment with glibenclamide resulted in 44.26% higher HOS tail-coiled sperm as compared to non-treated diabetic rats. Glibenclamide treatment was 1.65 times more potent than 250 mg/kg/day C. borivilianum in causing increased percentage of HOS tail coiled sperm in diabetic rats.
Effect on sperm morphology and percentages of abnormal sperm
Percentage of different types of abnormal sperm in different experimental groups
250 mg/kg C. borivilianum
500 mg/kg C. borivilianum
600 μg/kg glibenclamide
1.03 ± 0.02
8.63* ± 1.05
5.78† ± 0.26
4.82† ± 1.09
8.35† ± 1.06
13.15 ± 2.24
8.65 ± 1.09
7.52 ± 1.05
5.89 ± 0.85
Rod less sperm
9.84 ± 1.34
3.16 ± 0.22
2.17 ± 0.07
3.53 ± 0.16
Pin less sperm
6.39 ± 1.58
2.85 ± 0.11
2.65 ± 0.04
5.18 ± 0.27
Folded tail sperm
1.53 ± 0.03
3.35* ± 0.37
2.59† ± 0.06
0.81† ± 0.06
3.66† ± 0.34
Other shaped sperm
1.15 ± 0.18
1.25 ± 0.05
1.34 ± 0.05
2.08 ± 0.05
Effect on sperm MDA content
Effect on hydrogen peroxide and nitric oxide level in sperm
Effect on Sperm Total Antioxidant Capacity (TAC)
Effect of C. borivilianum on sperm endogenous antioxidant enzymes
Effect of C. borivilianum on SOD, CAT and GPx levels in the sperm of different experimental groups
250 mg/kg C. borivilianum
500 mg/kg C. borivilianum
600 μg/kg glibenclamide
Superoxide dismutase (units/mg protein/min)
1.56 ± 0.06
0.95* ± 0.07
1.26† ± 0.08
1.42† ± 0.06
1.45† ± 0.07
Catalase (H2O2 metabolized/mg protein/min)
0.64 ± 0.06
0.34* ± 0.08
0.45† ± 0.06
0.52† ± 0.05
0.56† ± 0.07
Glutathione peroxidase (μmol of GSH consumed/ mg protein/min)
1.72 ± 0.05
1.26* ± 0.08
1.57† ± 0.05
1.64† ± 0.06
1.66† ± 0.07
In-vitro free radical scavenging activity of C. borivilianum root extract
Figure 7(C) shows dose–response curve for hydroxyl radical scavenging activity of the root extract of C. borivilianum and ascorbic acid. IC50 for C. borivilianum root extract was 44.92 μg/ml while for ascorbic acid was 31.87 μg/ml. The IC50 for the root extract was 1.41 times lower than ascorbic acid. Hydroxyl radical is a major active oxygen species formed in the biological system with capability to conjugate with nucleotides in the DNA resulting in strand breakage which could lead to various diseases. Moreover, hydroxyl radical is one of the rapid initiator of lipid peroxidation process via extracting hydrogen atom from the unsaturated fatty acids . Figure 7(D) illustrates a dose-dependent increase in H2O2 scavenging activity of C. borivilianum root extract and ascorbic acid. IC50 of the root extract of C. borivilianum was 51.82 μg/ml while for ascorbic acid was 32.86 μg/ml. The IC50 for ascorbic acid was higher than the root extract by 1.58 times. H2O2 is a weak oxidizing agent that directly inactivates few enzymes via oxidation of essential thiol (-SH) group. This molecule could rapidly transverses the cell membrane. Once within the cell, H2O2 can react with Fe2+and /or Cu2+ to form hydroxyl radical .
Our results showing nitric oxide scavenging activity of C. borivilianum root extract and ascorbic acid standard are presented in Figure 7(E). The root extract of C. borivilianum root exhibits a dose-dependent increase on nitric oxide scavenging activity. IC50 for the root extract and ascorbic acid were 65.32 μg/ml and 31.45 μg/ml, respectively. IC50 of C. borivilianum root extract was lower than ascorbic acid by 2.08 times. NO is a free radical with a single unpaired electron, formed from L-arginine by the action of NO synthase . In the present study, the root extract of C. borivilianum showed a significant radical scavenging effect on nitric oxide. Finally, the reducing power scavenging activity of the root extract and ascorbic acid are shown in Figure 7(F). At 10 μg/ml, the percentage inhibition of C. borivilianum root extract and ascorbic acid were 32.68% and 38.67% respectively. IC50 of the root extract was 18.46 μg/ml while that of ascorbic acid was 13.54 μg/ml. Reducing power IC50 of C. borivilianum root extract was lower than ascorbic acid by 1.36 times.
Fasting blood glucose and serum HbA1c levels
FBG and serum HbA1c levels in different experimental groups
250 mg/kg C. borivilianum
500 mg/kg C. borivilianum
600 μg/kg glibenclamide
Fasting blood glucose levels (mg/dl)
93.15 ± 6.78
424.16* ± 7.23
235.24† ± 6.78
216.73† ± 4.84
203.68† ± 8.46
Glycosylated hemoglobin, HbA1c (%)
3.46 ± 0.39
9.38* ± 0.72
6.73† ± 0.61
5.17† ± 0.56
5.12† ± 0.43
Epididymal sperm density assessment
Assessment of epididymal sperm density
250 mg/kg C. borivilianum
500 mg/kg C. borivilianum
600 μg/kg glibenclamide
Epididymis sperm density
Caspase-3 level in sperm homogenates
To the best of our knowledge, this study reported for the first time the effect of root extract of C. borivilianum on sperm characteristics and oxidative stress in diabetic rats. Higher sperm count, percentages of sperm forward motility, viability and HOS tail-coiled with lower percentage of abnormal sperm were observed following C. borivilianum root extract treatment to STZ-induced diabetic rats. Administration of the root extract also lower the percentage of sperm with abnormal appearances, and in few occasion, the herbal root extract effect exceeds glibenclamide, a reference anti-diabetic drug . Our findings have further shown that C. borivilianum root extract was able to lower the level of sperm oxidative stress as evident from lower amount of lipid peroxidation product, MDA, tissue superoxide and nitric oxide free radicals and higher amount of total antioxidant capacity (TAC) and levels of endogenous antioxidant enzymes (SOD, CAT and GPx) in the sperm of diabetic rats. Treatment with C. borivilianum root extract also prevents the increase in serum level of FBG and HbA1c in diabetic rats where this might help to prevent negative effects of hyperglycemia on sperm.
An evaluation of sperm characteristics is useful when investigating the underlying cause of male infertility . In the present study, C. borivilianum root extract administration to diabetic rats prevented or reduced impairment in sperm characteristics, abnormal sperm percentages and abnormal appearances of sperm. The effect of diabetes on these sperm end point parameters was consistent with other reports in both rats and humans [45–47]. In diabetic rats, average sperm count of approximately 45million/ml was lower than normal (approximately 60 milllion/ml per ejaculate) [19, 48, 49]. Oligozoospermia could predispose diabetic males to subfertility or infertility . The observed decrease in sperm count was supported by diminished sperm intensity in the epididymal lumen. Treatment with C. borivilianum root extract has resulted in higher sperm count and epididymal sperm density which suggests that this herb protect the sperm against diabetes-induced damage. In this study, lower percentage of forward moving sperm was also observed in diabetic rats as compared to normal, non-diabetic rats. Sperm with normal forward motility are capable of swimming through the female reproductive tract and ultimately fertilized the oocyte. This characteristic is largely acquired during sperm transit and storage in the epididymis . Several factors including cAMP, intracellular pH and Ca2+ level could affect ability of the sperm to display these characteristics . Further studies are required to investigate oxidative stress parameters in testis, epididymis and seminal fluid which would help to ascertain their contribution towards the increase in sperm oxidative stress which subsequently caused sperm damage.
The percentage of sperm viability was also reduced in diabetic rats consistent with reports in both rodents [51, 53] and humans . Kanter et al.,  reported that in rats, diabetes could induce sperm apoptosis which resulted in reduced sperm viability. Similarly, higher caspase-3 expression was observed in this study which indicates increased sperm apoptosis in diabetes. 28-days treatment with C. borivilianum root extract to diabetic rats resulted in higher percentage of HOS tail-coiled sperm and lower percentage of abnormal sperm as well as sperm with various abnormal shapes. The reduced in percentage of HOS-tail coiled sperm which indicate inability of the sperm to display tail-coiled appearance upon placing into hypoosmotic solution  suggest reduced integrity of flagella membrane . Besides membrane integrity assessment, HOS tail coiled test is also useful to evaluate sperm viability . The reduced sperm viability which was parallel to the reduced appearance of HOS-tail coiled sperm has been reported in both diabetic rodents  and humans . Our finding which indicates reduced expression of caspase-3 in sperm of diabetic rats following C. borivilianum root extract treatment suggested that increased sperm viability was due to decreased in apoptosis. We speculated that the reduced appearance of HOS tail coiled sperm in diabetic rats could be due to increased in caspase-3, however this need further confirmation.
Diabetes induces oxidative-stress has been reported to cause peroxidation of sperm membrane lipid which might interfere with membrane fluidity and transport processes . In view of this, appearance of various abnormal sperm shapes could be due to abnormal membrane or cellular and nuclear changes induced by diabetes . More studies are needed to elucidate mechanisms underlying abnormal sperm appearances in diabetes. Treatment with C. borivilianum root extract prevents the increase in the amount of sperm lipid peroxidation as well as the levels of superoxide and nitric oxide free radical in sperm of diabetic rats. In both diabetic rats  and humans , lipid peroxidation was the major cause for sperm damage. Administration of C. borivilianum root extract to diabetic rats alleviates oxidative stress via several mechanisms which include reduced amount of free radicals such as superoxide and nitric oxide and preservation of total antioxidant capacity via maintaining near normal activity level of endogenous antioxidant enzymes. Additionally, a strong in-vitro free radical scavenging activity of the root extract further contribute towards the in-vivo free radical scavenging effects. The later effects may be attributed to higher amount of total phenolic content in the root extract as revealed by FTIR spectroscopic analysis. Meanwhile, ability of C. borivilianum root extract to lower FBG and HbA1c levels in diabetic rats could also help to reduce the risk of acquiring abnormal sperm morphology and characteristics and sperm oxidative stress [55, 59]. Scarano et al.  reported that sperm counts in diabetic rats was diminished following short-term exposure to hyperglycemia, while Amaral et al.  reported that prolonged hyperglycemia in rats adversely affect sperm concentration and motility due to oxidative stress.
The root extract of C. borivilianum is potentially useful for male infertility treatment via overcoming impairment in sperm characteristics and via reducing percentage and appearance of abnormal sperm in diabetes. Additionally, the root extract also prevents elevation of sperm oxidative stress that might trigger apoptosis. Our findings therefore justify the claimed beneficial effects of C. borivilianum root extract on sperm in diabetes.
This study was funded by UMRG grant (UMRG – RP011-13HTM) University of Malaya, Kuala Lumpur, Malaysia.
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