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JOURNAL CLUB PRESENTATION
HERBAL FORMULATION FOR ERECTILE
DYSFUNCTION IN MALE
APURVA K PAWAR
DEPARTMENT OF PHARMACOLOGY
AISSMS COLLEGE OF PHARMACY PUNE
UNDER GUIDANCE OF MRS.SWATI KOLHE MAM
AGENDA
 Objective
 Abstract
 Aim of experiment
 Risk factors with drugs
 Mechanism of ED
 PHF
 Method
 Statistical results
 Conclusion
 Reference
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OBJECTIVE
 Discuss the etiologies and the pathophysiology of
erectile dysfunction (ED)
 Describe the mechanism of action of agents used
to treat ED
 Recommend pharmacologic and non-
pharmacologic treatment for ED
 Identify drug interactions and adverse effects of
currently used medications for ED
 Identify treatment related side effects.
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ABSTRACT
 Erectile dysfunction (ED) is common among ageing
men because of associated underlying risk factors
which are peculiar to this category of patients.
 Endothelial dysfunction and replacement of
cavernosal smooth muscles by collagen fibres are
common in older men, making them prone to ED.
 Desmodium canum (Strong Back) is used for
experiment.
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AIM OF THE EXPERIMENT
 To identify the various phytochemicals present
within extracts of D. canum, their antioxidant
capabilities and their effects on blood glucose
levels, haemodynamic parameters and testosterone
levels( erectile dysfunction) in healthy Sprague-
Dawley (S-D) rats.
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RISK FACTORS
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Mechanism Of ED
HERBAL FORMULATION
 Desmodium canum (Strong Back) is deemed a
versatile traditional medicine, where it is used to
treat diabetes, hypertension, asthma and erectile
dysfunction.
 it is extensively used in aphrodisiac tonics, where it
is believed to increase libido by increasing
testosterone production and penile erection.
 PHF – Passion flower+ Tribulus terrestris +
ginkgo biloba (1:1:1).
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 The male primary sex hormone, testosterone, plays
a significant role in the erectile responses in men.
Studies have shown that men with higher
testosterone levels typically have a greater sex
drive.
 Additionally, the hormone up-regulates the
expression of the endothelium nitric oxide synthase,
an enzyme responsible for the synthesis of NO.
 Theoretically, this suggests that an increase in
testosterone levels may decrease the incidence of
erectile dysfunction due to oxidative stress in
diabetic men.
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MATERIALS AND METHODS
 Materials- Solvents (HPLC or ACS grade),
glucose and corn oil ,sodium hydroxide, ferric
chloride (GR Grade), hydrochloric acid, ammonium
molybdate, sulfuric acid , ACCU-Check Active
Blood Glucose Monitoring System, water bath B-
481, Spectroline MiniMax UV Lamp (Model UV-
4NFW), Kent CODA 6 non invasive blood Pressure
System (Monitor, animal restraints, electrical
warming pad and O- and V-cuffs), Analytical
Balance, Ohaus triple beam balance).
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1. Plant collection
2. Phytochemical Screening
3. Test for alkaloid,flavonoid,saponin glycosides,
tannis , saponins, tritepenoids.
 ETHICAL CONSIDERATIONS
 ANIMAL CARE
1
MEHTODS
11
RESULTS
 The effects of the crude extracts on testosterone levels
 Thirty-six male S-D rats were obtained from the Animal
House and divided into six groups with n = 6.
 By oral gavage
 group 1- was administered 250 mg/kg body weight
(BW) of the hexane extract dissolved in 0.3 mL corn oil.
 Group 2 was given the ethyl acetate extract (250 mg/kg
BW), again dissolved in 0.3 mL corn oil. Group 3
received the methanol extract (250 mg/kg BW)
dissolved in 0.3 mL of 10% dimethylsulfoxide (DMSO)
1
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1
 Groups 4 and 5- served as negative controls where the
carrier solvent, corn oil and DMSO were respectively
administered to the two groups.
 Groups 1–5 were treated daily for a period of 28 days
by oral administration of the respective treatment regime
described above..
 Group six served as a positive control in which the rats
received a 5 mg/kg BW per week treatment of
testosterone via subcutaneous injections. After 28 days
of treatment, all the rats were weighed and then
anaesthetized by intraperitoneal injections of sodium
pentobarbital (60 mg/kg BW). Blood was then collected
from the renal arteries, centrifuged at 3000 rpm for 10
min. Serum was removed and used for the quantification
of testosterone using a testosterone mouse/rat ELISA
kit.
13
STATISTICAL RESULT
 The hexane extract (2.21 ± 0.44 ng/mL) and testosterone
(2.99 ± 0.31 ng/mL) both showed significant increase in the
serum testosterone levels when compared with corn oil
control. There was no significant difference between the
hexane extract and the testosterone treated groups. The ethyl
acetate crude extract showed no significant difference to the
control indicating no effect on the testosterone level. There
was no significant difference between the methanol extract
and its control. Indicating no effect on the testosterone level.
The testosterone treated group was significantly higher than
these two groups. Qualitative analysis of the hexane extract
indicated the presence of steroids, alkaloids and terpenoids.
This significantly increased the serum testosterone levels in
the animals, where the values were comparable with the
testosterone treated group. Several studies have established
that many plants such as Moringa ol
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 oleifera and Tribulus alatus are aphrodisiacs, where they
typically increase testosterone level and/or inhibit the
phosphodiesterase-5 enzyme [24, 25]. Low testosterone
levels can be as a result of chronic illnesses, stress, trauma,
lifestyle, congenital issues, among others. The use of
testosterone as a therapeutic agent to infertility, erectile
dysfunction, athletic performance and low libido is well
documented. Exogenous testosterone, however, has many
side effects which include suppression of intratesticular
testosterone development, which is required for
spermatogenesis [26]. The effect of the crude hexane extract
in increasing the production and secretion of testosterone is
an ideal approach to treating hypogonadism in men, which is
a common cause of ED. However, a prudent approach is
necessary in establishing a method that utilizes this plant in
the treatment of hypogonadism,Ed,low sex drive.
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STATISTICAL RESULTS
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CONCLUSION
 The different extracts showed varying
pharmacological activities, that is, the hexane
extract significantly increased serum testosterone
levels in normal male rats.
1
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REFERENCE
1. The phytochemical and pharmacological
screening of three crude extracts of Desmodium
canum (strong back) Ruby Lisa Alexander-Lindo1*
, Roy Barrington Reynolds Porter2 ,
Chuckwuemeka Rapheal Nwokocha3 and
Kemmoy Godfrey Lattibeaudiere1.
1
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1
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erectile dysfunction in male

  • 1. JOURNAL CLUB PRESENTATION HERBAL FORMULATION FOR ERECTILE DYSFUNCTION IN MALE APURVA K PAWAR DEPARTMENT OF PHARMACOLOGY AISSMS COLLEGE OF PHARMACY PUNE UNDER GUIDANCE OF MRS.SWATI KOLHE MAM
  • 2. AGENDA  Objective  Abstract  Aim of experiment  Risk factors with drugs  Mechanism of ED  PHF  Method  Statistical results  Conclusion  Reference 1 2
  • 3. OBJECTIVE  Discuss the etiologies and the pathophysiology of erectile dysfunction (ED)  Describe the mechanism of action of agents used to treat ED  Recommend pharmacologic and non- pharmacologic treatment for ED  Identify drug interactions and adverse effects of currently used medications for ED  Identify treatment related side effects. 1 3
  • 4. ABSTRACT  Erectile dysfunction (ED) is common among ageing men because of associated underlying risk factors which are peculiar to this category of patients.  Endothelial dysfunction and replacement of cavernosal smooth muscles by collagen fibres are common in older men, making them prone to ED.  Desmodium canum (Strong Back) is used for experiment. 1 4
  • 5. AIM OF THE EXPERIMENT  To identify the various phytochemicals present within extracts of D. canum, their antioxidant capabilities and their effects on blood glucose levels, haemodynamic parameters and testosterone levels( erectile dysfunction) in healthy Sprague- Dawley (S-D) rats. 1 5
  • 8. HERBAL FORMULATION  Desmodium canum (Strong Back) is deemed a versatile traditional medicine, where it is used to treat diabetes, hypertension, asthma and erectile dysfunction.  it is extensively used in aphrodisiac tonics, where it is believed to increase libido by increasing testosterone production and penile erection.  PHF – Passion flower+ Tribulus terrestris + ginkgo biloba (1:1:1). 1 8
  • 9.  The male primary sex hormone, testosterone, plays a significant role in the erectile responses in men. Studies have shown that men with higher testosterone levels typically have a greater sex drive.  Additionally, the hormone up-regulates the expression of the endothelium nitric oxide synthase, an enzyme responsible for the synthesis of NO.  Theoretically, this suggests that an increase in testosterone levels may decrease the incidence of erectile dysfunction due to oxidative stress in diabetic men. 1 9
  • 10. MATERIALS AND METHODS  Materials- Solvents (HPLC or ACS grade), glucose and corn oil ,sodium hydroxide, ferric chloride (GR Grade), hydrochloric acid, ammonium molybdate, sulfuric acid , ACCU-Check Active Blood Glucose Monitoring System, water bath B- 481, Spectroline MiniMax UV Lamp (Model UV- 4NFW), Kent CODA 6 non invasive blood Pressure System (Monitor, animal restraints, electrical warming pad and O- and V-cuffs), Analytical Balance, Ohaus triple beam balance). 1 10
  • 11. 1. Plant collection 2. Phytochemical Screening 3. Test for alkaloid,flavonoid,saponin glycosides, tannis , saponins, tritepenoids.  ETHICAL CONSIDERATIONS  ANIMAL CARE 1 MEHTODS 11
  • 12. RESULTS  The effects of the crude extracts on testosterone levels  Thirty-six male S-D rats were obtained from the Animal House and divided into six groups with n = 6.  By oral gavage  group 1- was administered 250 mg/kg body weight (BW) of the hexane extract dissolved in 0.3 mL corn oil.  Group 2 was given the ethyl acetate extract (250 mg/kg BW), again dissolved in 0.3 mL corn oil. Group 3 received the methanol extract (250 mg/kg BW) dissolved in 0.3 mL of 10% dimethylsulfoxide (DMSO) 1 12
  • 13. 1  Groups 4 and 5- served as negative controls where the carrier solvent, corn oil and DMSO were respectively administered to the two groups.  Groups 1–5 were treated daily for a period of 28 days by oral administration of the respective treatment regime described above..  Group six served as a positive control in which the rats received a 5 mg/kg BW per week treatment of testosterone via subcutaneous injections. After 28 days of treatment, all the rats were weighed and then anaesthetized by intraperitoneal injections of sodium pentobarbital (60 mg/kg BW). Blood was then collected from the renal arteries, centrifuged at 3000 rpm for 10 min. Serum was removed and used for the quantification of testosterone using a testosterone mouse/rat ELISA kit. 13
  • 14. STATISTICAL RESULT  The hexane extract (2.21 ± 0.44 ng/mL) and testosterone (2.99 ± 0.31 ng/mL) both showed significant increase in the serum testosterone levels when compared with corn oil control. There was no significant difference between the hexane extract and the testosterone treated groups. The ethyl acetate crude extract showed no significant difference to the control indicating no effect on the testosterone level. There was no significant difference between the methanol extract and its control. Indicating no effect on the testosterone level. The testosterone treated group was significantly higher than these two groups. Qualitative analysis of the hexane extract indicated the presence of steroids, alkaloids and terpenoids. This significantly increased the serum testosterone levels in the animals, where the values were comparable with the testosterone treated group. Several studies have established that many plants such as Moringa ol 1 14
  • 15.  oleifera and Tribulus alatus are aphrodisiacs, where they typically increase testosterone level and/or inhibit the phosphodiesterase-5 enzyme [24, 25]. Low testosterone levels can be as a result of chronic illnesses, stress, trauma, lifestyle, congenital issues, among others. The use of testosterone as a therapeutic agent to infertility, erectile dysfunction, athletic performance and low libido is well documented. Exogenous testosterone, however, has many side effects which include suppression of intratesticular testosterone development, which is required for spermatogenesis [26]. The effect of the crude hexane extract in increasing the production and secretion of testosterone is an ideal approach to treating hypogonadism in men, which is a common cause of ED. However, a prudent approach is necessary in establishing a method that utilizes this plant in the treatment of hypogonadism,Ed,low sex drive. 1 15
  • 17. CONCLUSION  The different extracts showed varying pharmacological activities, that is, the hexane extract significantly increased serum testosterone levels in normal male rats. 1 17
  • 18. REFERENCE 1. The phytochemical and pharmacological screening of three crude extracts of Desmodium canum (strong back) Ruby Lisa Alexander-Lindo1* , Roy Barrington Reynolds Porter2 , Chuckwuemeka Rapheal Nwokocha3 and Kemmoy Godfrey Lattibeaudiere1. 1 18
  • 19. 1 19