Content uploaded by Zaib Ur Rehman
Author content
All content in this area was uploaded by Zaib Ur Rehman on Jul 10, 2015
Content may be subject to copyright.
Veterinaria 2015 | Volume 3 | Issue 1 | pages 32-39
32
Abstract
Antibiotic growth promoters have been extensively used in the poultry feed to improve weight gain, feed efficiency, lessen the
number of harmful bacteria, enhance immunity etc. However, they have role in development of the resistance in the pathogenic
bacteria and impose negative impact on the consumers due to residues. Medicinal plants are the best replacement option of
ABGP. Garlic is the king of the medicinal plants which have growth promoting effect in chicken production. It has antibacterial,
antiviral, antifungal and antiprotozoal properties. Moreover, it boosts the immune system, improves the body weight gain,
heighten the digestibility of ingredients, decrease the bad cholesterol, and also augment the meat quality parameters. This article
describes the detail about the use of garlic in poultry feed which can enhance the productivity and can attain the growth
promotion potential without causing adverse effects unlike antibiotic growth promoters.
Keywords: Garlic, Poultry, Feed, Immunity, Growth promoter
Key words:
Received May 15, 2015; Revised June 19, 2015; Accepted June 28, 2015
*Corresponding author: Muhammad Tanveer Munir E-mail: muhammadtanveermunir765@gmail.com
Review paper
Effect of garlic on the health and performance of broilers
Zaib ur Rehmana, Muhammad Tanveer Munirb*
aDepartment of Poultry Science, FV&AS, PMAS Arid Agriculture University, Rawalpindi. 46300, Pakistan
bPoultry and Wildlife Section, National Agricultural Research Centre, Islamabad. 46000, Pakistan
To cite this manuscript: Rehman Z, Munir MT. Effect of garlic on the health and performance of broilers. Veterinaria 2015;
3(1): 32-39.
Introduction
Feed additives are added in poultry feed to
improve nutritive value of ingredients and enhance
broiler performance by increasing growth rate and
improving feed conversion efficiency. Chemical
feed additives e.g. Antibiotic growth promoters
(ABGP), have been intensively used in broiler’s
ration to improve productivity. However, they are
notorious for bacterial resistance and their negative
impacts on the consumers’ health [1]. Thus, use of
ABGP has been banned in poultry industry. Now,
nutritionists are shifting from chemical growth
promoter to phytogenic growth promoters. Thus,
it is important to explore the potential of innate
feed additives to replace the chemical ones. Herbs
could be expected to serve as feed additives due to
their suitability and preference, lower cost of
production, reduced risk of toxicity, minimum
health hazards and environment friendliness [2].
Recent research works on phytogenic feed
additives have shown promising results as regards
weight gain, feed efficiency, lowered mortality and
increased livability in poultry birds [3-7].
Phytogenic substances are supposed to increase
performance of birds by stimulating secretion of
digestive enzymes, leading to enhanced digestion
and absorption [8, 9]. Furthermore, the presence of
active ingredients and phenolic compounds can
reduce numbers of intestinal pathogens, thus
minimizing nutrient loss and improving
performance. Both effects may result in better
intestinal health and may lead to more protein
deposition in body tissues. But, the effects of
active ingredients on performance and health of
animals are in-consistent, as affected by the
number of environmental and agronomical factors
leading to differences in amount and activities of
active ingredients. In literature, no clear-cut effect
of phytogenic compounds on performance
parameters in different species of poultry has been
reported.
Herbs spices like garlic (Allium sativum) have
been reported to possess useful pharmacological
substances [10]. Freshly crushed garlic contains
allicin, alliin, ajoene, diallylsulfide, dithiin, S-
allylcysteine. Garlic as natural feed additives in
poultry nutrition may be of great benefit and value
especially for broiler growers. This is due to their
antibacterial, anti-inflammatory, antiseptic, anti-
parasitic and immunomodulatory properties of
garlic. In Pakistan, farmers are already using this
specie in scavenger poultry feed to attain the
aforementioned results.
Garlic is used as flavoring agent in different
dishes and medicament, antioxidant,
antihypertensive, anti-ageing, hypo-lipidaemic,
anti-platelet and detoxify the heavy metal [11, 12].
Due to its antimicrobial properties, garlic is the
highly studied medicinal plant used as growth
promoter in broiler chickens [13, 14]. Therefore,
trials have evaluated garlic as an alternative of
growth promoters in poultry and revealed its
Veterinaria 2015 | Volume 3 | Issue 1 | pages 32-39
33
excellent effects on growth, digestibility and
carcass characteristics [15].
The objective of this article is to gather the
large amount of research literature into a refined
summery so that it can be used as guideline for
standard development of garlic use in poultry. For
this purpose, antimicrobial and performance
enhancing properties of garlic has been discussed
in this review.
Antimicrobial properties
Use of garlic and ginger as a medicine and
condiment goes back to written history. It is
thought that these are originated in traditions of
both India and China. Egyptian medical papyrus,
Codex Ebers, interpreted in 1937; has more than
800 medical formulations, of which 22 contains
garlic.
Recently the first evidence of its antimicrobial
properties was established when four men were
employed to remove the dead bodies during a
plague in Marseilles in 1721 in France. None of
them became infected. When research is done to
identify the secret then it was known that they use
garlic and wine tincture [16]. The precursor alliin,
a cysteine sulfoxide, and the corresponding
alliinase enzyme are the main components of
garlic [17]. Garlic has been used for centuries in
many countries to control infectious diseases. It
has been used to prevent wound infection and food
spoilage in India [18].
Antibacterial affects
Historically it is believed that Louis Pasteur first
scientist who demonstrate the antimicrobial effects
of garlic ‘juices’ in 1858, however, no reference is
available. Recently it is proved that garlic is
effective against many acid-fast, gram-positive and
gram-negative bacteria. These include Escherichia
coli (E. Coli), Salmonella [19], Clostridium [20],
Staphylococcus aureus, Pseudomonas, Proteus
[21], Klebsiella [22], Micrococcus, Bacillus
subtulis [23] and Helicobacter [24]. So, garlic can
be used to treat Colibacillosis, Salmonellosis and
Cholera in poultry. Garlic exerts a differential
inhibition between beneficial intestinal microflora
and potentially harmful enterobacteria [25]. For
the same garlic dose inhibition zone observed in E.
coli was more than 10 times than that seen in
Lactobacillus casei [26]. The exact mechanism of
this differential inhibition is not known, but one of
the possible reasons may be the change in
chemical composition of membranes of different
bacteria and their absorptivity to allicin [27]. An
inhibitory synergism of antimicrobial properties of
garlic was observed when it was used in
combination with vancomycin [28].
Antiviral effects
Mostly the commercially available antibiotics are
not affective against viruses. That is the reason
these cannot be used to control the viral diseases of
poultry. Very less research is done on antiviral
properties of garlic compared to antibacterial.
Allicin and allicin-derived substances are active
against viruses and no activity has been indicated
with alliin or S-allyl cysteine. It has been proved
that garlic shows in vitro activity against influenza
A and B viruses, rhinovirus, HIV, herpes simplex
virus 1 and 2, cytomegalovirus, viral pneumonia
and rotavirus [29-33].
Anti-protozoal Affects
Use of garlic in poultry feed exhibits antiprotozoal
effects in poultry but the exact mechanism of
action remains to be explored. Several studies have
shown that it is effective against a host of protozoa
including Opalina ranarum, Entamoeba
histolytica, Balantidium entozoon, O. dimidicita,
Trypanosomes, Leishmania, and Leptomonas [34].
Diallyl trisulfide a component of garlic is
commercially available in many countries like
China in commercial preparation named Dasuansu
and has been prescribed for treatment of diseases
caused by Trichomonas vaginalis and Entamoeba
histolytica [35]. Allicin, ajoene and organosulfides
are the main components of garlic which have
antiprotozoals properties. Thiol content of
microbial cells are not quite enough, to
counterbalance the thiol oxidation by allicin and
allicin-derived products that why these are more
affected than animal cells [34].
Antifungal effects
Alike other antimicrobial properties antifungal
activity of garlic has also been proven to be
thanksgiving. The first ever report of antifungal
activity of garlic in epidermophyte cultures was
Veterinaria 2015 | Volume 3 | Issue 1 | pages 32-39
34
reporterd by Schmidt and Marquardt [36]. Studies
suggest that garlic can prevent the growth of
Aspergillus, Torulopsis, Trichophyton,
Cryptococcus, Candida, Trichosporon and
Rhodotorula [37-39]. Garlic has oxygen scavenging
molecules which decrease the oxygen uptake [40],
reduce the growth of the organism, stops the
synthesis of protein, lipids, and nucleic acids [41]
and denature the membranes [42]. A sample of pure
allicin was shown to be antifungal. Solvent
extraction of allicin from garlic decreased the
antifungal activity [43]. Activity has also been
observed with diallyl trisulfide against cryptococcal
meningitis [44], and ajoene, against Aspergillus
[45], Candida [46].
Broiler Growth Performance
Many scientists investigated the effects of long
term feeding of garlic and its’ preparations on the
performance of broilers. Most of these studies
reported a statistically significant improvement in
cumulative feed conversion ratio. Garlic increases
growth and improves feed conversion ratio [47] by
increasing height of villus of small intestine,
activation of absorption process. To support these
ideas a study has proven that dietary fermented
garlic supplementation in broiler ration can
increase the intestinal villus height, villus area, cell
area, cell mitosis in the intestine and results in
better feed efficiency [48].
Serum cholesterol
Garlic, being the king of medicinal plants, imposes
beneficial effects on body metabolites. Several
clinical studies have supported this idea [49-52].
Allicin may reduce the levels of serum cholesterol,
triglyceride and LDL [53]. Diets comprising garlic
powder has ability to lower down serum and egg
cholesterol level in hens [54]. An investigation has
reported that supplementation of garlic powder at
the levels of 0, 2, 6 and 8% does not affect the egg
weight, egg mass, feed consumption and feed
efficiency in the laying hens [55]. However,
lowering effect on the serum and egg yolk
cholesterol concentrations was observed with
dietary garlic [56]. Garlic paste, solvent-extracted
fractions or garlic oil reduced the concentration of
serum cholesterol by 23% and 18% in twelve
week-old Leghorn pullets and broilers,
respectively, when diets were fed for 4 week [57].
Decrease in hepatic cholesterol concentration in
chickens was observed when 2% garlic was fed for
14 day [58]. Similar effects of garlic were found in
rats fed diets containing either cholesterol or
triglyceride [59].
The mechanism which involved in decreasing
the cholesterol, triglyceride and LDL is that it
reduces the activities of hepatic lipogenic and
cholesterogenic enzymes such as fatty acid
synthase, malic enzyme, 3-hydroxy-3-methyl-
glutaryl-CoA (HMG CoA) reductase and glucose-6
phosphate dehydrogenase [60]. Garlic also
increased the excretion of cholesterol, as
demonstrated by enhanced excretion of acidic and
neutral steroids after garlic feeding [61]. LDL
isolated from human, given aged garlic extract [62]
and aqueous garlic extract [63] was found to be
decisively more resistant to oxidation. Suppressed
LDL oxidation may be one of the controlling
mechanisms for the benefits of garlic in
atherosclerosis [64]. Allicin was identified initially
as the active compound responsible for depressing
the atherosclerotic effect. However, in vitro studies
revealed that organosulfur compounds especially,
diallyl-di-sulfide, present in garlic oil and water-
soluble S-allyl cysteine, present in aged garlic
extract are also potent inhibitors of cholesterol
synthesis [65].
Hematology
Garlic supplementation in poultry imposes positive
effects on hematological parameters of poultry
birds. Hematological analysis reported by Kung-chi
et al. [66] demonstrated that intake of garlic oil
significantly increased white blood cell and
reduced red blood cell counts, hemoglobin,
hematocrit and mean corpuscular hemoglobin
values in rats. Addition of garlic in diet of fish
increase the red blood cells and mean corpuscular
volume when it was used at the concentration of
20, 30 40g/Kg [67]. The scientists reported that
hematocrit values reached a significant increase in
fish fed on 20 g garlic but no significant differences
in mean corpuscular hemoglobin concentration was
noted.
It is also possible that the end product of garlic
metabolism in the body stimulates the kidney
directly to cause formation and secretion of
Veterinaria 2015 | Volume 3 | Issue 1 | pages 32-39
35
erythropoetin. Now, scientists are trying to
determine the effect of garlic on erythropoetin
level. Another experiment concluded that garlic
supplementation increases the white blood cells,
lymphocytes and immunoglobulin G in broilers
[68]. In contrast, it has been reported that garlic
does not affect leukocyte numbers in broilers [69].
With regards to WBC counts, it was reported that
dietary addition of garlic increased lymphocyte
concentration in peripheral blood of pigs. The
enhanced lymphocyte proliferation by garlic
treatment along with the possible protection of the
cells from oxidative stress seemed to contribute for
the increased WBC count [70-75].
Immune System
Although garlic kills viruses, bacteria and other
microorganisms directly, it also excites the body’s
natural defenses against these antigens. Garlic’s
amazing and famous power against diseases is due
to a combination of both these properties. Aged
garlic extracts have an immunomodulatory effect
and lessens the age-related deterioration of the
immune response. Garlic supplementation in
chickens increase the relative weights of the
spleen, bursa of Fabricius and thymus [68, 73].
In vitro garlic extracts excites the rat and
human lymphocytes. A protein fraction (F4),
isolated from aged garlic extract, boost the
cytotoxicity of human peripheral blood
lymphocytes against natural killer-sensitive and
resistant cell lines and induced lymphocyte
infiltration and cytokine release [74, 75].
Diallyltrisulfide and protein fraction, the
components of garlic has been shown to enhance
activation of T lymphocytes [76, 77] and also
progresses the ratio of helper to suppressor T cell
in AIDS. It also enhances antibody production
against Salmonella enteritidis, Pasteurella
multocida and Leptospira Pomona bacteria [78],
which indicate that it increase the activity of B
lymphocytes. Alliums at low levels in the diet
improved the humoral immune response against
Brucella abortus (non-replicating T-cell
independent antigen) in chickens [68].
Garlic extracts have been found to suppress
pro-inflammatory cytokines like IL-2 and elevate
inter lukin (IL) -10 and IL-12 in monocytes [79].
Garlic preparations encouraged the macrophage
infiltration and cytokine release. Garlic
components boost the immune stimulation by
mitogenic activation (e.g. allicin). Scientists have
reported that addition of garlic extract to a
macrophage culture of laying hens at 50 µg/mL
tended to enhance Sheep red blood cells uptake; on
the other hand, high concentration of the extract
(200 µg/mL) inhibited phagocytosis [80].
Experiments in humans and mice revealed that
addition of aged garlic extract to a culture
enhances the phagocytosis of peritoneal cells and
increases the production of interleukin (IL)-2, IL-
12, interferon-y and tumor necrosis factor-a from
spleenocytes [73], and the addition of different
garlic extracts enhances the engulfment ability of
phagocytes [81], as well as the secretory
metabolism of macrophages [77, 82, 83].
Aged Garlic Extract excites the proliferation of
spleen cells, release of cytokines and phagocytosis
(the ability of immune cells to engulf foreign
agents) of peritoneal macrophages. Immune
enhancing effects of commercial garlic
preparations was studied and it was found that
aged garlic extract was the most effective for
improving immune factors, specifically
macrophage and T-lymphocyte activity [84].
Hanieh et al. [68] reported supplementing
chickens with garlic exerted enhancing effect on
the humoral immune responses against Newcastle
disease virus and sheep RBC (non-replicating T
cell-dependent antigens). It has been studied that
supplementing broilers with a liquid product
including garlic, feed acidifier and microbial cell
extract increase antibody production against
Newcastle disease vaccine [78] and infectious
bursal disease vaccine [85, 86]. These
inconsistencies in the results may be due to
preparation method of the garlic. However, there
might be possibility that immunomodulatory
property could be antigen- dependent [87, 88].
Aged Ginger has antibacterial properties and kills
cold viruses so, indirectly stimulate the immune
system. Nidaullah et al. [89] concluded that
aqueous extract of garlic bulb and ginger (Zingiber
officinale) rhizome plays a very important role as
immunstimulant against Coccidiosis, Newcastle
disease, Infectious bronchitis and infectious bursal
disease.
Veterinaria 2015 | Volume 3 | Issue 1 | pages 32-39
36
Carcass Characteristics
One of the new insights in poultry industry is to
improve the quality of meat with nutrition
modelling. Alteration in the quality of intact
muscle is possible by nutrition. Direct addition of
antioxidants or feed additives to improve the
quality of meat are too effective because these
compounds are not deposited in the muscles where
these are required and this can be done by adding
them in the feed [90].
To prevent the oxidative deterioration of meat
by free radicals, antioxidants have been
extensively used as feed additives. Synthetic
antioxidants are extensively used for industrial
processing in order to prolong the storage stability
of meat. Antioxidants like butylated
hydroxyanisole and butylated hydroxytoluene have
been widely rejected by the consumers due to their
supposed carcinogenic potential as demonstrated
by toxicologists [91]. Rejection to synthetic food
additives by the consumer has been increasing in
advanced countries. That’s why scientists are
searching for the natural additives which have the
greatest potential of anti-oxidation.
Garlic supplementation has an antioxidant
effect that is why lowers the thiobarbituric acid-
reactive substance value and might protect lipid
oxidation [68]. Garlic has many kinds of
antioxidant compounds such as flavonoid and
sulfur containing compounds [92]. Besides,
Leonarduzzi et al. [93] reported that LDL particles
may have significant amount of cholesterol
oxidation products. Therefore, the decrease in LDL
cholesterol could also mirror the antioxidant
effects of garlic supplementation. The anti-
oxidative impact of garlic in meat becomes more
authoritative in less developed nations, considering
storage problems and increasing use of alternative
feed resources without due consideration for meat
quality [94]. By using garlic as feed additive in
broiler ration we can get the bioactive components
in meat that directly cannot be consumed by
human.
Research findings indicated that pH plays a
significant role in the extent of microbial spoilage
[95]. Glycogen concentration in muscle is the main
factor on which pH relies. If birds are exposed to
stress before slaughtering then glycogen is
depleted in the muscles [96]. Meat having higher
pH, holds more water during storage and will
produce more juice after meat preparation. If more
juice is produced from the meat then it will give
juicier, more succulent and tender eating
experience. The pH values of chicken sausage can
be increased by the treatment of garlic [97]. The
pH of meat of finishing pigs can also be increased
by garlic treatment [98].
Conclusion
Garlic is king of medicinal plants and it has
wondrous effects in poultry. The garlic
supplementation of poultry feed has shown better
performance of birds, ultimately enhancing the
production potential. Additionally, garlic reduces
the number of pathogenic bacteria like
Campylobacter, E. coli and Salmonella,
clostridium, etc. It has beneficial effects on
consumer’s immunity. So, it can be effectively
used to replace the antibiotic growth promoter in
poultry feed. Although, there is huge pile of
research literature in this area, but still there is a
need to establish standards of garlic use in poultry
feed. To fulfill this purpose more research is
needed in this economics friendly supplement.
References
[1] Rehman, Z., and Haq, A. Effect of garlic and ginger
supplementation on broiler performance.Lambert Publishing
Company. 2014.
[2] Devegowda, G. Herbal medicines, an untapped treasure in
poultry production. In: Proc. 20th World Poult. Congr. New
Delhi, India. 1996.
[3] Kumar OM. Effect of Liv-52® syrup on broiler performance
in North Eastern region. Indian Poult Rev 1991; 22: 37-38.
[4] Babu M, Gajendran K, Sheriff FR, Srinivasan G. Crown
Growfit® supplementation in broilers improved their
performance. Indian Poult Rev 1992; 23: 27-28.
[5] Mishra SJ, Singh DS. Effect of feeding root powder of
Withania somnifera (L.) Dunal (aswagandha) on growth, feed
consumption, efficiency of feed conversion and mortality rate
in broiler chicks. Bioved 2000; 11: 79-83.
[6] Deepak G, Jogi S, Kumar A, Bais R, Vikas KS. Effect of
herbal liver stimulants on efficacy of feed utilization in
commercial broiler chicken. Indian J Anim Res 2002; 36: 43-
45.
[7] Jahan ZA, Ahsan UH, Muhammad Y, Tanveer A, Sarzamin
K. Evaluation of different medicinal plants as growth
promoters for broiler chicks. Sarhad J Agric 2008; 24: 323-
329.
[8] Geier U, Oster A. Kräuter–Eine Alternative zu antibiotischen
Leistungsförderern. DGS-Magazin 2001; 22: 35-40.
[9] Recoquillay F. Active plant extracts show promise in poultry
production. Poult Int 2006; 28-30.
Veterinaria 2015 | Volume 3 | Issue 1 | pages 32-39
37
[10] Akhtar MS, Afzal H, Chaudhary F. Preliminary in vitro
antibacterial screening of Bakain, Gilo and Zarisk against
Salmonella. Medicos 1984; 9: 6-7.
[11] Agarwal KC. Therapeutic action of garlic constituents. Med
Res Rev 1996; 16: 111-124.
[12] Marilynn L. Effect of garlic on blood lipids in particles with
coronary heart disease. Am J Clin Nutr 2001; 34: 2100-2103.
[13] Freitas R, Fonseca JB, Soares RTRN, Rostango HS Soares
PR. Utilization of garlic (Allium sativum L.) as growth
promoter of broilers. Rev Bras Zootecn 2001; 30: 761-765.
[14] Lewis MR, Rose SP, Mackenzie AM, Tucker LA. Effects of
dietary inclusion of plant extracts on the growth performance
of male broiler chickens. Brit Poult Sci 2003; 44: 43-44.
[15] Bampidis VA, Christodoulou V, Christaki E, Florou-Paneri
P, Spais AB. Effect of dietary garlic bulb and garlic husk
supplementation on performance and carcass characteristics
of growing lambs. Anim Feed Sci Technol 2005; 121: 273-
283.
[16] Hann G. History, folk medicine, and legendary uses of garlic.
In: Koch HP, Lawson LD (eds) Garlic: the science and
therapeutic application of Allium sativum L. and related spe-
cies. Williams and Wilkins, Baltimore. 37-107. 1996.
[17] Stoll V, Seebeck E. Allium compounds. I. Alliin, the true
mother compound of garlic oil. Helv Chem Acta 1948; 31:
189.
[18] Arora SD, Kaur J. Antimicrobial activity of spices. J
Antimicrob Agents 1999; 12: 257-262
[19] Johnson MG, Vaughn RH. Death of Salmonella typhimurium
and Escherichia coli in the presence of freshly reconstituted
dehydrated garlic and onion. Appl Microbiol 1969; 17: 903-
905.
[20] De Witt JC, Notermans S, Gorin N Kampelmacher EH.
Effect of garlic oil or onion oil on toxin production by
Clostridium botulinum in meat slurry. J Food Protect 1979;
42: 222-224.
[21] Cavallito CJ, Bailey JH. Allicin, the antibacterial principle of
Allium sativum. I. Isolation, physical properties and
antibacterial action. J Am Chem Soc 1944; 66: 1950-1951.
[22] Jezowa L, Rafinski, Wrocinski T. Investigations on the
antibiotic activity of Allium sativum L. Herba Pol 1966; 12:
3-13.
[23] Sharma VD, Sethi MS, Kumar A, Rarotra JR. Antibacterial
property of Allium sativum Linn. In vivo and in vitro studies.
Indian J Exp Biol 1977; 15: 466-468.
[24] O’Gara EA, Hill DJ, Maslin DJ. Activities of garlic oil, garlic
powder, and their diallyl constituents against Helicobacter
pylori. Appl Environ Microbiol 2000; 66: 2269-2273.
[25] Rees LP, Minney SF, Plummer NT, Slater JH, Skyrme DA.
A quantitative assessment of the anti-microbial activity of
garlic (Allium sativum). World J Microbiol Biotechnol 1993;
9: 303-307.
[26] Skyrme DA. The antimicrobial activity of Allium sativum.
PhD Thesis, Cardiff University, UK. 1997.
[27] Miron T, Rabinkov A, Mirelman D, Wilchek H, Weiner L.
The mode of action of allicin: its ready permeability through
phospholipid membranes may contribute to its biological
activity. Biochem Biophys Acta 2000; 1463: 20-30.
[28] Jonkers D, Sluimer J, Stobberingh E. Effect of garlic on
vancomycin resistant enterococci. Antimicrob. Agents
Chemother. 1999; 3043-3045.
[29] Fenwick GR, Hanley AB. The genus Allium. CRC Crit Rev
Food Sci Nutr 1985; 22: 199-377.
[30] Tsai Y, Cole LL, Davis LE, Lockwood SJ, Simmons V, Wild
GC. Antiviral properties of garlic: in vitro effects on
influenza B, herpes simplex virus, and coxsackie viruses.
Planta Med 1985; 51: 460-461.
[31] Weber ND, Anderson DO, North JA, Murray BK, Lawson
LD, Hughes BG. In vitro virucidal activity of Allium sativum
(garlic) extract and compounds. Planta Med 1992; 58: 417-
423.
[32] Meng Y, Lu D, Guo N, Zhang L, Zhou G. 1993. Anti-HCMV
ef¬fect of garlic components. Virol Sin 1993; 8: 147-150.
[33] Nai-Lan G, Cao-Pei L, Woods GL, Reed E, Gui-Zhen Z, Li-
Bi Z, Waldman RH. Demonstration of antiviral activity of
garlic extract against human cytomegalovirus in vitro. Chin
Med J 1993; 106: 93-96.
[34] Reuter HD, Koch HP, Lawson LD. Therapeutic effects and
applications of garlic and its preparations. In: Koch HP,
Lawson LD., ed Garlic: The science and therapeutic
application of Allium sativum L. and related species.
Williams and Wilkins, Baltimore. :135-213. 1996.
[35] Lang YJ, Zhang KY. Studies on the effective components of
garlic (Allium sativum L.). Chin Herb Med 1981; 4: 4-6.
[36] Schmidt PW, Marquardt U. Über den antimykotischen efffekt
ätherischer öle von lauchgewächsen und kreuzblütlern auf
pathogene. Hautpilze. Zentralbl. Bakteriol. Parasitenkd.
Infektionskrankh. Hyg Abrst 1936; 138: 104-128.
[37] Hitokoto H, Morozumi S, Wauke T, Sakai S, Kurata H.
Inhibitory effects of spices on growth and toxin production of
toxigenic fungi. Appl Environ Microbiol 1980; 39: 818-822.
[38] Fromtling RA, Bulmer GS. In vitro effect of aqueous garlic
extract (Allium sativum) on the growth and viability of
Cryptococcus neoformans. Mycologia 1978; 70: 397-405.
[39] Tansey MR, Appleton JA. Inhibition of fungal growth by
garlic extract. Mycologia 1975; 67: 409-413.
[40] Szymona M. Effect of phytoncides of Allium sativum on the
growth and respiration of some pathogenic fungi. Acta
Microboil Pol 1952; 1: 5-23.
[41] Adetumbi MA, Javor GT, Lau BHS. Allium sativum (garlic)
inhibits lipid synthesis by Candida albicans. Antimicrob
Agents Chemother 1986; 30: 499-501.
[42] Ghannoum MA. Studies on the anticandicidal mode of
ac¬tion of Allium sativum (garlic). J Gen Microbiol 1988;
134: 2917- 2924.
[43] Hughes BG, Lawson LD. Antimicrobial effect of Allium
sativum L. (garlic) Allium ampeloprasum (elephant garlic),
and Allium cepa L. (onion), garlic compounds and
commercial garlic supplement products. Phytol Res 1991; 5:
154–158.
[44] Cai Y. Anticryptococcal and antiviral properties of garlic.
Cardiol Pract 1991; 9: 11.
[45] Yoshida S, Kasuga S, Hayashi N, Ushiroguchi T, Matsuura
H, Nakagawa S. Antifungal activity of ajoene derived from
garlic. Appl Environ Microbiol 1987; 53: 615-617.
[46] Ghannoum MA. Inhibition of Candida adhesion to buccal
epithelial cells by an aqueous extract of Allium sativum
(garlic). J Appl Bacteriol 1990; 68: 163-169.
[47] Tollba AAH, Hassan MSH. Using some natural additives to
improve physiological and productive performance of broiler
chicks under high temperature conditions. 2. Black cumin
(Nigella sativa) or garlic (Allium sativum). Poult Sci 2003;
23: 327-340.
[48] Incharoen T, Yamauchi K, Thongwittaya N. Intestinal villus
histological alterations in broilers fed dietary dried fermented
ginger. J Anim Physiol Anim Nutr (Berl) 2010; 94: 130-137.
[49] Grundy SM, Bilheimer D, Blackburn H, Brown VW,
Kwiterovich PO, Mattson F, Chonfeld G, Weidman WH.
Rationale of the diet-heart statement of the American Heart
Veterinaria 2015 | Volume 3 | Issue 1 | pages 32-39
38
Association. Report of the Nutrition Committee. Circulation
1982; 65: 839-854.
[50] Mensink RP, Katan MB. Effect of dietary fatty acids on
serum lipids and lipoproteins: a meta-analysis of 27 trials.
Arterioscler Thromb 1992; 12: 911-919.
[51] Katan MB, Grundy SM, Willett WC. Beyond low-fat diets. N
Eng J Med 1997; 337: 563-566.
[52] Warshafsky S, Kamer RS, Sivak SL. Effects of garlic on total
serum cholesterol. A meta-analysis. Ann Intern Med 1993;
119: 599-605.
[53] Alder AJ, Holub BJ. Effect of garlic and fish-oil
supplementation on serum lipid and lipoprotein
concentrations in hypercholesterolemic men. Am J Clin Nutr
1997; 65: 445-450.
[54] Mottaghitalab M, Taraz Z. Effects of garlic (Allium sativum)
on egg yolk and blood serum cholesterol in Aryan breed
laying hens. Brit Poult Sci 2002; 43: 42-43.
[55] Khan SH, Hasan S, Sardar R, Anjum MA. Effects of dietary
garlic powder on cholesterol concentration in Native Desi
laying hens. Am J Food Tech 2008; 3: 207-213.
[56] Chowdhury SR, Chowdhury SD, Smith TK. Effects of
dietary garlic on cholesterol metabolism in laying hens. Poult
Sci 2002; 81: 1856-1862.
[57] Qureshi AA, Din ZZ, Abuimeileh N, Burger WC, Ahmad Y,
Elson CE. Suppression of avian hepatic lipid metabolism by
solvent extracts of garlic: Impact on serum lipids. J Nutr
1983; 113: 1746-1755.
[58] Sklan D, Bermer YN, Rabinowitch HD. The effect of dietary
onion and garlic on hepatic lipid concentrations and activity
of antioxidative enzymes in chicks. J Nutr Biochem 1992;
3:322-325.
[59] Myung SC, Enusook TK, Stewart TJ. Effects of garlic on
lipid metabolism in rats fed cholesterol or lard. J Nutr 1982;
112: 241-248.
[60] Yeh Y-Y, Liu L. 2001. Cholesterol lowering effect of garlic
extracts and organosulfur compounds: Human and animal
studies. J Nutr 131: 989-993.
[61] Chi MS, Koh ET, Stewart TJ. Effect of garlic on lipid
metabolism in rats fed cholesterol or lard. J Nutr 1982; 112:
241-248.
[62] Munday JS, James KA, Fray LM, Kirkwood SW, Thompson
KG. Daily supplementation with aged garlic extract, but not
raw garlic, protects low density lipoprotein against in vitro
oxidation. Atherosclerosis 1999; 143: 399-404.
[63] Lewin G, Popov I. Antioxidant effects of aqueous garlic
extract. 2nd communication: Inhibition of the Cu (2+)-
initiated oxidation of low density lipoproteins.
Arzneimittelforschung 1994; 44: 604-607.
[64] Lau Benjamin HS. Suppression of LDL oxidation by garlic. J
Nutr 2001; 131: 958-988.
[65] Gebhardt R, Beck H. Differential inhibitory effects of garlic-
derived organosulfur compounds on cholesterol biosynthesis
in primary rat hepatocyte cultures. Lipids 1996; 31: 1269-
1276.
[66] Kung-chi C, Mei-chin Y, Wan-Ju C. Effect of diallyl
trisulfide-rich garlic oil on blood coagulation and plasma
activity of anticoagulation factors in rats. Food Chem Toxicol
2006; 45: 502-507.
[67] Shalaby AM, Khattab YA, Rahman MA. Effects of garlic
(Allium sativum) and chloramphenicol on growth
performance, physiological parameters and survival of nile
tilapia (Oreochromis niloticus). J Venomous Anim Toxins
Incl Trop Dis 2006; 12: 172-201.
[68] Hanieh H, Kiyoaki N, Mingzi P, Chaogetu G, Asaki A,
Yasuhiro K. Modulatory effects of two levels of dietary
alliums on immune response and certain immunological
variables, following immunization, in White Leghorn
chickens. Anim Sci J 2010; 81:673-680.
[69] Ao X, Yoo JS, Zhou TX, Wang JP, Meng QW, Yan L, Cho
JH, Kim IH. Effects of fermented garlic powder
supplementation on growth performance, blood profiles and
breast meat quality in broilers, Livest Sci 2011; 141: 85-89.
[70] Jafari RA, Jalali MR, Ghorbanpoor M, Saraei MRM. Effect
of dietary garlic on immune response of broiler chicks to live
Newcastle disease vaccine. Pak J Biol Sci 2008; 11: 1848-
1851.
[71] Chen Y, Kim I, Cho J, Yoo J, Wang Q, Wang Y, Huang Y.
Evaluation of dietary L-carnitine or garlic powder on growth
performance, dry matter and nitrogen digestibilities, blood
profiles and meat quality in finishing pigs. Anim Feed Sci
Tech 2008; 141: 141-152.
[72] Onu PN. Evaluation of two herbal species as feed additives
for finisher broilers. Biotech Anim Husb 2010; 26: 383-392.
[73] Kyo E, Uda N, Kasuga S, Itakura Y. Immunomodulatory
effects of aged garlic extract. J Nutr 2001; 131: 1075-1079.
[74] Morioka N, Sze LL, Morton DL, Irie RF. Protein fraction
from aged garlic extract enhances cytotoxicity and
proliferation of human lymphocytes mediated by interleukin-
2 and concanavalin A. Cancer Immunol Immunother 1993;
37: 316-322.
[75] Colic M, Savic M. Garlic extracts stimulate proliferation of
rat lymphocyte in vitro increasing IL-2 and IL-4 production.
Immunopharmacol Immunotoxicol 2000; 22: 163-181.
[76] Feng ZH, Zhang GM, Hao TL, Zhou B, Zhang H, Jiang ZY.
Effect of diallyl trisulfide on the activation of T cell and
macrophage-mediated cytotoxicity. J Tongi Med Univ China
1994; 14: 142-147.
[77] Lau B, Yamasaki T, Gridley D. Garlic compounds modulate
macrophage and T-lymphocyte functions. Mol Bioth 1991; 3:
103-107.
[78] Szigeti G, Pálfi V, Nagy B, Iné E, Nagy G, Szmolény G,
Bagó G, Radványi S. New type of immune stimulant to
increase antibody production generated by viral and
bac¬terial vaccines. Magyar Allatorvosok Lapja 1998; 120:
719–721.
[79] Hodge G, Hodge S, Han P. Allium sativum (garlic)
suppresses leukocyte inflammatory cytokine production in
vitro: potential therapeutic use in the treatment of
inflammatory bowel disease. Cytometry 2002; 48: 209.
[80] Dorhoi A, Dobrean V, Zahan M, Virag P. Modulatory effects
of several herbal extracts on avian peripheral blood cell
immune responses. Phytotherapy Research 2006; 20: 352-
358.
[81] Romano E, Montano R, Brito B, Apitz R, Alonso J, Romano
M, Gebran S, Soyano A. Effects of ajoene on lymphocyte
and macrophage membrane-dependent functions.
Immunopharmacol Immunotoxicol 1997; 19: 15-36.
[82] Dirsch V, Kiemer A, Wanger H, Vollmar M. Effects of
allicin and ajoene, two compounds of garlic, on inducible
nitric oxide synthase. Atherosclerosis 1998; 139: 333-339.
[83] Gomez-Flores R, Calderon C, Scheibel L, Tamez-Guerra P,
Rodriguez-Padilla C, Tamez-Guerra R, Weber R.
Immunoenhancing properties of Plantago major leaf extract.
Phytoth Res 2000; 14: 617-622.
[84] Tadi P, Teel RW, Lau B. Anticandidal and anticarcinogenic
potentials of garlic. Int Clin Nutr Rev 1990; 10: 423-429.
[85] Gabor S, Vilmos P, Bela N, Istvanne E, Gyorgy N, Gabor S,
Gyorgy B, Szabolcs R. New type of immuno-stimulant to
increase antibody production in response to viral and
Veterinaria 2015 | Volume 3 | Issue 1 | pages 32-39
39
bacterial vaccines. Magyar Allatorvosok Lapja 1998; 120:
719-721.
[86] Chinnah AD, Baig MA, Tizard IR, Kemp MC. Antigen
dependent adjuvant activity of a poydispersed beta-(1,4)-
linked acetylated mannan (acemannan). Vaccine 1992; 10:
551-557.
[87] Taheri HR, Rahmani HR, Pourreza J. Humoral immunity of
broilers as affected by Oil Extracted Propolis (OEP) in the
diet. Int J Poult Sci 2005; 4: 414-417.
[88] Nidaullah H, Durrani FR, Ahmad S, Jan IU, Gul S. Aqueous
extract from different medicinal plants as anticoccidial,
growth promotive and Immunostimulant in broilers. ARPN J
Agri Bio Sci 2010; 1: 53-59.
[89] Govaris A, Botsoglou N, Papageorgiou G, Botsoglou E,
Amvrosiadis I. Dietary versus postmortem use of oregano oil
and/ or a-tocopherol in turkeys to inhibit development of
lipid oxidation in meat during refrigerated storage. Int J Food
Sci Nutr 2004; 55: 115-123.
[90] Reishe DW, Lillard DA, Eitenmiller PR. Antioxidants in
food lipids. In: Ahoh, C.C., Min, D.B. (ed.). Chemistry
Nutrition and Biotechnology. Marcel Dekker, New York,
423-448, 1998.
[91] Gorinstein S, Drzewieki J, Leontowicz H, Leontowicz M,
Najman K, Jastrzebski Z. 2005. Comparison of the bioactive
compounds and antioxidant potentials of fresh and cooked
Polish Ukrainian, and Israeli garlic. J Agric Food Chem
2005; 53: 2726-2731.
[92] Leonarduzzi G, Sottero B, Poli G. Oxidized products of
cholesterol: dietary and metabolic origin, and
proatherosclerotic effects: a review. J Nutr Biochem 2002;
13: 700-710.
[93] Onibi GE, Agbede JO, Afun ST, Aletor VA. Assessment of
the meat quality of broiler chickens fed equi-protein
replacement of fish meal with frog meal. Res Agric Sci 2007;
1: 73-80.
[94] Rey CR, Kraft AA, Topel DG, Parrish FC, Hotchkiss DK.
Microbiology of pale, dark, and normal pork. J Food Sci
1976; 41: 111-116.
[95] Ngoka DA, Froning GW. Effect of free struggle and
preslaughter excitement on color of turkey breast muscles.
Poult Sci 1982; 61: 2291-2293.
[96] Sallam KI, Ishioroshi M, Samejima K. Antioxidant and
antimicrobial effects of garlic in chicken sausage. Lebensm
Wiss Technol 2004; 37: 849-855.
[97] Holden PJ, Mckean J, Brandenburg E. Biotechnicals for pigs-
Garlic (ASLR1559). ISU Swine Research Report. Iowa State
University, Ames. 1998.