Role of Micronutrients in the Management of Male Infertility
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Transcript of Role of Micronutrients in the Management of Male Infertility
Role of Micronutrients in the
Management of Male Infertility
Final Diagnostic Categories in a Male Infertility Clinic
Diagnosis No %
Varicocele
Idiopathic
Obstruction
Normal/Female factor
Cryptorchidism
Immunologic
Ejaculatory dysfunction
Testicular failure
Drug/Radiation
Endocrinologic
Infection
Sexual dysfunction
Systemic disease
Sertoli -cell-only
Ultrastructural defect
Genetic
Testis cancer
603
324
205
113
49
36
18
18
16
16
13
4
4
3
3
2
2
42.2
22.7
14.3
7.9
3.4
2.6
1.3
1.3
1.1
1.1
0.9
0.3
0.3
0.2
0.2
0.1
0.1
Total 1,430 100.0 (Stigman et al. 1997)(Stigman et al. 1997)
Treatment of Male InfertilityTreatment of Male Infertility
1. Medical Therapy
2. Surgical Therapy Varicocelectomy
Vasovasostomy Vasoepididymostomy
TUR of ejaculatory duct
obstruction
3. Assisted Reproductive Technology (ART)
Sperm processing, IUI, IVF
4. Artificial Insemination
of Donor (AID)
Medical TherapyMedical Therapy
I.I. According to evidence According to evidence dependencydependency
Specific Medical TherapySpecific Medical Therapy Non-specific Empirical Medical Non-specific Empirical Medical
TherapyTherapy
II. According to drugII. According to drug Hormonal therapyHormonal therapy Non-hormonal therapyNon-hormonal therapy
Criteria for SuccessCriteria for Success• Duration : 3~6 months, at least one full spermatogenic cycleDuration : 3~6 months, at least one full spermatogenic cycle• Parameter : Semen analysis & hormonal assayParameter : Semen analysis & hormonal assay
: Criteria -: Criteria - count 30%, motility 20% (Lee et al. 1986)count 30%, motility 20% (Lee et al. 1986)
VolumeVolume >2.0ml>2.0ml
pHpH >7.2>7.2
Sperm concentrationSperm concentration >20×10>20×1066/ml /ml >15 million>15 million
Total sperm countTotal sperm count >40×10>40×1066/ejaculate/ejaculate
MotilityMotility >50% (grade a+b) or >25% (grade a)>50% (grade a+b) or >25% (grade a)
MorphologyMorphology >15% by strict criteria >15% by strict criteria 10%10%
ViabilityViability >75%>75%
WBCWBC <1×10<1×1066/ml/ml
WHO criteria of normal semen, 1999WHO criteria of normal semen, 1999
Specific Medical TherapySpecific Medical Therapy
Endocrine Disorder
Pyospermia
Immunologic Infertility with Antisperm Ab
Retrograde Ejaculation
Nonspecific Empirical Medical TherapyNonspecific Empirical Medical Therapy
Hormonal TherapyHormonal TherapyGnRHGnRH
GonadotropinGonadotropin
TestosteroneTestosterone
AntiestrogenAntiestrogen
Aromatase inhibitorAromatase inhibitor
Growth hormone Growth hormone
Iatrogenic oligospermiaIatrogenic oligospermia
Refractory to specific medical therapyRefractory to specific medical therapy
Adjuvant therapy before and after 1Adjuvant therapy before and after 1stst line therapeutic modality line therapeutic modality
Preliminary therapy prior to ARTsPreliminary therapy prior to ARTs
Non-hormonal TherapyNon-hormonal TherapyCarnitineCarnitine
KallikreinKallikrein
PentoxyphyllinePentoxyphylline
NSAIDsNSAIDs
αα-blocker-blocker
ClonidineClonidine
MisellaneousMisellaneous
Difficult Cases for Empirical Medical Treatment
1. Shrunken testicle (volume < 10ml)1. Shrunken testicle (volume < 10ml)
2. Histopathological findings of testis biopsy2. Histopathological findings of testis biopsy
: Sertoli cell only syndrome: Sertoli cell only syndrome
Severe maturation arrest (Johnson score 3-4)Severe maturation arrest (Johnson score 3-4)
3. Azoospermia or severe oligospermia (1.0 3. Azoospermia or severe oligospermia (1.0
× 10× 1066ml)ml)
: especially, Increased FSH to twice normal: especially, Increased FSH to twice normal
Pitfall in Comparison among Results of Empirical Medical Therapy
• No placebo controlled double blind trials No placebo controlled double blind trials
• Heterogenous patients population Heterogenous patients population
• Variable dosages, treatment period and follow-up Variable dosages, treatment period and follow-up
• Tremendous fluctuation in an individual Tremendous fluctuation in an individual
semen parameter semen parameter
• Different criteria for success Different criteria for success
Newer concepts
Reactive Oxygen Species in Male InfertilityReactive Oxygen Species in Male Infertility
I. ROS generation in semenI. ROS generation in semen
: About 40% in infertile men (Iwasaki & Gagnon, 1992): About 40% in infertile men (Iwasaki & Gagnon, 1992)
II. Harmful action mechanism of ROS on spermII. Harmful action mechanism of ROS on sperm
by overwhelming endogenous antioxidant defensesby overwhelming endogenous antioxidant defenses
1. Cause sperm membrane lipid peroxidation1. Cause sperm membrane lipid peroxidation
2. Decrease membrane fluidity2. Decrease membrane fluidity
3. Reduce sperm motility3. Reduce sperm motility
4. Decrease sperm-oocyte fusion capability4. Decrease sperm-oocyte fusion capability
5. Impair fertilizing capacity5. Impair fertilizing capacity
ROS and Male Infertility
Reactive Oxygen Species isone of the majorcontributors to male Infertility & cause Damage to the sperm
• Cell membrane
• DNA molecules
• Lipids
• Proteins
Urology. 1996;48(6):835–850.
Endogenous ROS Formation and Direct Scavenging Endogenous ROS Formation and Direct Scavenging Effect of Antioxidant in Sperm CellEffect of Antioxidant in Sperm Cell
antioxydantantioxydantInfectionRadiationChemotherapypollution
Intrinsic antioxidant : SOD, catalase, ascorbate, tocopherolIntrinsic antioxidant : SOD, catalase, ascorbate, tocopherolManagement 1) Extrinsic antioxidant : Vit A, C, E, glutathione, selenium, Management 1) Extrinsic antioxidant : Vit A, C, E, glutathione, selenium, rebamipiderebamipide 2) Sperm washing with culture media including antioxidant 2) Sperm washing with culture media including antioxidant to removal leukocyteto removal leukocyte
Genetic Causes
• DNA damage and mutations in mitochondrial DNA have
been linked to poor sperm motility and male subfertility.
• A genetic factor located at Yq11 has been established to
be important for male germ cell development and Yq11
damage may lead to male infertility.
• Deletions of AZFa, AZFb and AZFc (Microdeletions in the
Y-chromosome) can result in male infertility.
• Klinefelter’s syndrome, Kallman’s syndrome can also
result in male infertilityIndian J Med Res. 2008;127:124-132.J. Biosci. 2001;26(4):492-435.
Environmental Causes
Various environmental factors can result in male infertility. The factors
are as follows:
• Infection
• Excessive heat
• Radiation exposure
• Heavy metal toxicity
• Cigarette smoking
• Xeno-estrogen exposure
• Pesticides and other chemicals
Altern Med Rev. 2000;5(1):28-38.
Human Reproduction, 2001;16(8):1768-1776.
http://www.gfmer.ch/Endo/Fellows_11/Pdf/Infertility_environment.pdfHuman Reproduction, 2001;16(8):1768-1776.
Occupationally Free time
Physical activity Prolonged sitting
Thermoregulation of scrotumelevation of scrotal temperature
HEAT EXPOSURE
Spermatogenesis
Quality and quantity of sperm production(count, morphology, motility, delayed coception)
Sedentary lifestyle
Environmental Causes
Nutritional Considerations
Various micronutrients are
associated with male
fertility.
Deficiency of these
micronutrients may result
in infertility.
Nutritional Factors
Free radical scavengers
L-Carnitine
Lycopene
Coenzyme Q10
Vitamin C
Zinc Vitamin E
Arginine Glutathione
Vitamin B12
Selenium
Altern Med Rev. 2000;5(1):28-38.
Role of Micronutrients in Fertility
Nutrition plays vital role in maintaining male fertility:
• Involved in the successful maturation of sperm
• Provides nutrition for motility of sperm
• Improvement in sperm count and motility
• Helps in production of sex hormones
• Prevents sperm damage
Altern Med Rev. 2000;5(1):28-38.
Non hormonal TherapyNon hormonal Therapy
: To improvement of Sperm motility : To improvement of Sperm motility
Sperm fertilizing capacitySperm fertilizing capacity
Sperm metabolismSperm metabolism
Testicular microcirculationTesticular microcirculation
1. Carnitine1. Carnitine
2. Kallikrein2. Kallikrein
3. Pentoxyphylline3. Pentoxyphylline
4. NSAIDs4. NSAIDs
5. 5. αα-blocker-blocker
6. Clonidine6. Clonidine
7. Miscellaneous 7. Miscellaneous
• CoQ10 is a naturally-occurring compound found in every cell in the body.
• Coenzyme Q10 (CoQ10) is concentrated in the mitochondrial mid-piece
• CoQ10's alternate name is ubiquinone
• It is found in foods, particularly in fish and meats
• Coenzyme Q10 (CoQ10) acts as an electron carrier in the mitochondrial respiratory chain.*
*CLIN. CHEM. 41/2, 217-219 (1995) **Chem Scripta 1987;27:145-58
Co enzyme Q10
Free Radical
Scavenger
Energizer
CLIN. CHEM. 41/2, 217-219 (1995)
Co enzyme Q10 - Mechanism
• In sperm cells, coenzyme Q10 (CoQ10) is
concentrated in the mitochondria.
• Coenzyme Q10 is responsible for energy for movement and all other energy-dependent processes in the sperm cell.
• Reduction in levels of CoQ10 is observed in sperm cells and seminal plasma of idiopathic (IDA) and varicocele- associated (VARA) asthenozoospermic patients.*
• It is observed that sperm cells, characterized by low motility and abnormal morphology, have low levels
of CoQ10.*Andrologia 34 (2002), 107–111.
Co enzyme Q10 - Mechanism
• Administration of CoQ10 increased the pregnancy rate by 36% and with improvement of sperm
count and functional sperm concentration in 70% and 60%
individuals, respectively.
• Sperm motility and sperm motility index improved in 54% and 46 % while 38 % showed improvement
in sperm morphology.
Folia Med (Plovdiv).2005;47(1):26–30.
Coenzyme Q10: Clinical Trials
Improvement in sperm motility, motilityIndex and sperm morphology
Sperm Morphology
Motilityindex
Sperm Motility
• Patients – 22 infertile men with idiopathic asthenozoospermia.
• Coenzyme Q10 - 200 mg for 6 months
• A significant increase was also found in sperm cell motility
Conclusion:
• The exogenous administration of CoQ(10) may play a positive role in the treatment of asthenozoospermia.
• This is probably the result of its role in mitochondrial bioenergetics and its antioxidant properties.Fertil Steril. 2004
Jan;81(1):93-8.
Coenzyme Q10: Clinical Trials
Coenzyme Q10: Clinical Trials
Lewin et al. showed that Coenzyme Q10 results in improvement in sperm functions in asthenospermic men
35.7
19.1
0
10
20
30
40
Imp
rove
men
t (%
)
Coenzyme Q10 Control group
Mean increase in motility: Coenzyme Q10 vs. control group
Coenzyme Q10: Improvement in fertilization rate
0
5
10
15
20
25
30
Baseline Day 103
Impr
ovem
ent (
%)
Mol Aspects Med 1997;18 S213-S219.
Coenzyme Q10: Clinical Trials
According to a review conducted by Langade et al. Coenzyme Q10 significantly increased sperm motility within 6 months.
Coenzyme Q10 and improvement in sperm motility
02468
1012141618
Baseline After 6 months
Impr
ovem
ent (
%)
Bombay hospital journal.
http://www.bhj.org/journal/april2005/htm/reveiw_coenzyme_145.htm
Non hormonal Therapy Non hormonal Therapy Carnitine Carnitine ::
◈◈ L- carnitine &L- carnitine & acetylcarnitineacetylcarnitine
◈◈ Intracellular energy metabolismIntracellular energy metabolism
Stabilization of cell wallStabilization of cell wall
◈◈
L-carnitine 2~3 gm/dayL-carnitine 2~3 gm/day
Acetylcarnitine 4 gm/dayAcetylcarnitine 4 gm/day
Change of L-carnitine & Acetylcarnitine in Seminal Plasma
I. In oligoasthenozoospermiaLower level of L-carnitine (Lewin et al, 1976)
Lower level of acetylcarnitine (Kohengkul et al, 1977)
II. Significant positive correlation between L-carnitine and sperm density & motility
(Menchini-Fabrisetal, 1984)
III. Reduction of acetylcarnitine/L-carnitine ratio
: low grade sperm motility (Bartelloni et al, 1987)
→ Rationale for using carnitine in the Tx of male infertility
L-Carnitine
• The main function of L-Carnitine in the epididymis is
to provide an energetic substrate for spermatozoa.
• May be involved in the successful maturation of
sperm.
• L-Carnitine is necessary for transport of fatty acids
into the mitochondria to produce energy.
• Low levels of L-Carnitine reduces fatty acid
concentrations within the mitochondria, leading to
decreased sperm motilityDrugs 1987;34:1-24.Arch Ital Urol Nefrol Androl 1992;64:187-196.
L-Carnitine
• Significantly high levels of free L-Carnitine is
observed in the seminal plasma of the fertile men
compared to the infertile men.
• The level of free L-Carnitine in the semen has positive
correlation with sperm concentration, sperm motility
and vitality of sperm cells
• L-Carnitine provides readily available energy for use
by spermatozoa, which positively affects sperm
motility, maturation and the spermatogenesis process. Folia Med (Plovdiv). 2005;47(1):26–30. . Zhonghua Nan Ke Xue. 2007;13(2):143–146.
L-Carnitine: Clinical Trials
According to a study conducted by Costa et al. L-carnitine
increased the sperm parameters drastically
10.8
28.4
3.73.1
142.4
1832.5
4.120.3
163.3
0
20
40
60
80
100
120
140
160
180
Baseline At 4 months
Motile spermatozoa (%)
Mean velocity (microns)
Linearity index
Spermatozoa with rapidlinear progression (%)
Number of ejaculatedspermatozoa
Andrologia.1994;26:155-159.
L- Carnitine for asthenospermia with varicocele
Carnitine
Placebo
Zhonghua Nan Ke Xue. 2004;10(9):671–672.
There was significant improvement in sperm count,motility and pregnancy rates in infertility due to varicocele.
Use of Carnitine therapy in selected cases of male factor infertility: A double-blind
crossover trial
• Patient(s): One hundred infertile patients
(ages 20–40 years) with the following baseline
sperm selection criteria: concentration, 10–20
X 106/mL; total motility, 10%–30%; forward
motility, <15%; atypical forms, <70%; velocity,
10–30 µ/s;
• Interventions : L-Carnitine therapy 2 g/day or
placebo;
• Duration : 4 monthsFERTILITY AND STERILITY VOL. 79, NO. 2, FEBRUARY 2003
Total motile sperm/mL
Carnitine
Placebo
FERTILITY AND STERILITY VOL. 79, NO. 2, FEBRUARY 2003
Forward motile sperm/mL
Carnitine
Placebo
FERTILITY AND STERILITY VOL. 79, NO. 2, FEBRUARY 2003
L- Carnitine in idiopathic asthenozoospermia: a multicenter study.
Italian Study Group on Carnitine and Male Infertility.
Andrologia 1994;26:155-159
N = 100 patients
L-carnitine - 3 g/day
Duration - 4 months.
Percentage of motile spermatozoa increased from 26.9 ± 1.1 to 37.7 ± 1.1 %.
Total number of spermatozoa per ejaculate also increased
Conclusion - Oral administration of L-Carnitine may improve sperm quality
Lycopene is a bright red
pigment and phytochemical
found in tomatoes and other
red fruits, water melon & guava.
Belongs to a class referred to as
carotenoids which are yellow,
orange, and red pigments
synthesized by plants
Lycopene
Lycopene possesses superior abilities in comparison to other carotenoids.
It has the ability to quench singlet oxygen and prevent oxidative damage to other molecules.
This is because of its unique structure of: 11 conjugated double bonds and no cyclic groups
Lycopene
The general mechanism by which Lycopene works is by preventing oxidative damage to sperms, which includes
• Damage to the cell membrane
• DNA molecules
• Lipids
• Proteins
Lycopene has been demonstrated to be the most potent antioxidant with the ranking: lycopene > α-tocopherol > α -carotene > β- carotene > lutein.
Lycopene – Biological activity
Lycopene supplementation in vivo & in
vitro protects cells from induced oxidative
damage
Lipid peroxidation is reduced by 80%
DNA oxidation is reduced by 75%
Matos et al, Arch Bioch Biophys 1999
Matos et al, Arch Bioch
Biophys 2000
Oral Lycopene supplementation protects
against ex vivo induced lymphocyte DNA
oxidation
DNA fragmentation (COMET assay) is
reduced by 40%Riso et al, Am J Clin Nutr
1999
Lycopene - Biological activity
Lycopene: Clinical Trials
66
5346
010203040506070
Impr
ovem
ent
(%)
Sperm
conc
entra
tion Mo
tility
Morph
ology
Lycopene in infertility
Int Urol Nephrol. 2002;34:369–372.
A Study evaluated
the effect of oral
lycopene therapy in
men with idiopathic
infertility.
Lycopene - 2000
mcg, twice a day
for three months
N - 30 Patients
Improvement in sperm concentration
Results
Improvement in sperm concentration - 20 patients
(66%)
Improved motility – 16 patients (53%)
Improvement in sperm morphology - 14 patients
(46%)
Associated with significant improvement and
resulted in six pregnancies in 26 patients (23%)
Conclusion - Lycopene therapy seems to have a
role in the management of idiopathic male
infertility
Zinc is a micronutrient abundantly present in meat and seafood and serves as a cofactor for more than 80 enzymes involved in DNA multiplication and protein synthesis
Zinc deficiency is associated with decreased testosterone levels & sperm count.
Zinc levels are generally lower in infertile men with diminished sperm count
Furthermore, zinc finger proteins are implicated in the genetic expression of steroid hormone receptors*, and zinc also has anti- apoptotic ** and antioxidant properties.***
*Endocr Rev 1992 :13,129–145. **Curr Drug Targets 2003:4,323–338. ***Free Radic Biol Med 31,266–274.
Zinc
Rev Prat. 1993;43:146-151.
Ann Nutr Metab. 1986;30:213-218.
The functions of zinc in male reproduction
Effects of zinc supplementation on subfertility
Zinc – Clinical Trials
N - 100 men with asthenozoospermia
Two groups--250 mg twice daily zinc therapy for 3 months and no therapy.
Duration – 6 months
There was significant improvement in the sperm quality; sperm count, progressive motility, fertilizing capacity
Conclusion: Zinc therapy has a role in improving sperm parameters in men with asthenozoospermia
Eur J Obstet Gynecol Reprod Biol. 1998 Aug;79(2):179-84.
• Netter et al. studied the effect of zinc
supplementation on testosterone,
dihydrotestosterone and sperm count.
• The results of the study were dramatic
Zinc – Clinical Trials
• 37 patients were studied• Testosterone and dihydrotestosterone levels
increased significantly • Nine wives became pregnant, six within 3 months
and three within 2 months
Zinc: Clinical Trials
According to study conducted by Tikkiwal et al.
zinc resulted in
• Significant improvement in sperm count,
• Number of progressively motile and normal
spermatozoa
• Normal acid phosphates activity. Indian J Physiol Pharmacol. 1987;31(1):30-34.
Arginine
• Arginine is thought to be essential for sperm motility.
• According to a study by Schachter et al. Arginine
significant improved sperm count and motility after
taking 4 g/day for three months.
• A recent study conducted in Italia also showed that
arginine is effective in male infertility
• However, the dosage of arginine is higher compared
to other micronutrients.J Urol 1973;110:311-313.Minerva Urol Nefrol 1994;46:251-253.
Selenium
• Selenium and glutathione are essential to the
formation of phospholipid hydroperoxide
glutathione peroxidase
• Deficiencies of selenium can lead to instability
of the mid-piece, resulting in defective motility
• However, it can be toxic if consumed in
excess.ArchAndrol. 1992;29:65-68. Science 1999;285:1393-1396.Environ Mol Mutagen. 2009 [Epub ahead of print]
Methylcobalamin
• Vitamin B12 is important in cellular replication,
especially for the synthesis of RNA and DNA, and
deficiency states have been associated with
decreased sperm count and motility.
• Various studies have shown that Methylcobalamine
improves the sperm parameters
• However, studies show that Methylcobalamine is
effective in only just over 20% of infertile men.Hinyokika Kiyo 1986;32:1177-1183.Hinyokika Kiyo. 1984;30:581-586.
Hinyokika Kiyo 1988;34:1109-1132.
Vitamin E
• Oral supplementation with vitamin E significantly
decreases the malondialdehyde concentration and
improves the sperm motility
• Although Invitro studies have prooved the efficacy of
vitamin E, human studies are lacking
• Although there are few human studies, they recruited
only few patients
Fertil Steril 1995;64:825-831.Biol Trace Elem Res 1996;53:65-83.Arch Androl 1992;29:65-68.
Nonhormonal Therapy Nonhormonal Therapy KallikreinKallikrein
· Kininogenase stimulate the release of kinins· Kininogenase stimulate the release of kinins
(bradykinin, kallidin, methionylkallidin) from (bradykinin, kallidin, methionylkallidin) from kininogenskininogens
→ → Increase vascular permeability, smooth m. Increase vascular permeability, smooth m. contraction contraction
& membrane glucose transport& membrane glucose transport
→ → Increase sperm motilityIncrease sperm motility
◈ ◈ 600 units/day, po600 units/day, po
Count 0~50% (25%)Count 0~50% (25%)
Motility 20~67% (43.5%)Motility 20~67% (43.5%)
Pregnancy 17~25% (16.3%)Pregnancy 17~25% (16.3%)
Nonhormonal Therapy Nonhormonal Therapy Penotoxifylline Penotoxifylline
Universal phosphodiesterase inhibitorUniversal phosphodiesterase inhibitor
: Inhibit the breakdown effect of c-AMP: Inhibit the breakdown effect of c-AMP
◈ ◈ 400mg, po, tid400mg, po, tid
Count 57%Count 57%
Motility 47%Motility 47%
Pregnancy 17%Pregnancy 17%
Nonhormonal Therapy Nonhormonal Therapy NSAIDsNSAIDs
◈◈ indomethacin, ketoprofen, diclofenac sodiumindomethacin, ketoprofen, diclofenac sodium◈◈ Inhibit prostaglandin with decreasing Inhibit prostaglandin with decreasing
testicular steroidogenesis, testicular steroidogenesis,
spermatogenesisspermatogenesis and sperm motilityand sperm motility◈◈ 150mg/day150mg/day
Nonhormonal TherapyNonhormonal Therapy αα-blocker-blocker
◈◈ Improve testicular circulationImprove testicular circulation
◈◈ Terazocin Terazocin 2~4mg/day , po2~4mg/day , po
doxazocindoxazocin
alfuzocinalfuzocin
Nonhormonal TherapyNonhormonal Therapy Clonidine Clonidine
◈ ◈ EEnhance secretion of Growth Hormonenhance secretion of Growth Hormone
◈ ◈ Clonidine 1.75mg/dayClonidine 1.75mg/day
◈◈ improvement 50%improvement 50%
Nonhormonal Therapy Nonhormonal Therapy Miscellaneous Miscellaneous
1. Bromocriptine mesylate, metergoline,
corticosteroids, thyroxine oxytocin
2. Folic acid, adenosine triphosphate (ATP) L-
glutamine
3. Serotonin
Clinical Effects of Nonspecific Medical TherapyClinical Effects of Nonspecific Medical Therapy
Drugs Drugs nono Improvement Improvement Pregnancy Pregnancy
nono %% nono %%
HCG + Amino acidsHCG + Amino acids
Folic acid & ZincFolic acid & Zinc
metergolinemetergoline
8585
103103
44
2626
7676
33
3131
7474
7575
1515 1818
L-arginineL-arginine
AlCAMINAlCAMIN
VitaminVitamin
SeleniumSelenium
4040
2929
5050
4545
1010
88
1414
44
2525
2828
2828
1111
55
55
66
1313
1717
1212
CarnitineCarnitine
KallikreinKallikrein
ClonidineClonidine
NSAIDsNSAIDs
αα-blocker-blocker
100100
6363
100100
1515
1818
3535
1515
3030
5050
3535
2525
1515
11
3535
1515
1414
5050
3535
2525
ClomipheneClomipheneTamoxifenTamoxifen
565699
181811
32321111
7711
13131111
The Quadruple of Atreya
• According to ancient sage Athreya, there are 4 components for a successful treatment
1. The Physician.
2. Drugs.
3. The Patient.
4. Attendants
It is told that all the 4 components have to be efficient to achieve successful treatment.
Charka Samhitha
Ideal Nutraceutical for Male Infertility
• Just like the Quadruple of Atreya, successful treatment of male
infertility should control all the aspects of sperm dysfunction
in infertile males.
An combination of L-Carnitine,
Coenzyme Q10, Lycopene and
Zinc can provide holistic approach to
male infertility
L-carnitine
Improves sperm motility by providing energy to the sperm cell through fatty acid metabolism
Zinc
Promotes sperm production & maturation testosterone synthesis & improves sperm morphology
Ideal Nutraceutical for Male Infertility
Coenzyme Q10
Improves sperm motility by providing energy through ATP generation in mitochondrion
Lycopene
Increases sperm count and improves morphology by reducing oxidative damage to sperm DNA and lipids
Thank you
What is an Ideal Choice in Male Infertility?