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Environmental Factors On Secondary Metabolism of Medicinal Plants
Environmental Factors On Secondary Metabolism of Medicinal Plants
Environmental Factors On Secondary Metabolism of Medicinal Plants
Mohi Uddin*
World University of Bangladesh, Bangladesh
*Corresponding Author: Mohi Uddin, World University of Bangladesh, Bangladesh.
Received: April 08, 2019; Published: July 11, 2019
DOI: 10.31080/ASPS.2019.03.0338
Abstract
Plants are unrivaled in the common world in both the number and unpredictability of secondary metabolites they produce, and
the pervasive phenylpropanoids and the heredity explicit glucosinolates speak to two such vast and artificially various gatherings.
Advances in genome-empowered natural chemistry and metabolomic innovations have incredibly expanded the comprehension
of their metabolic systems in assorted plant species. There additionally has been some advancement in explaining the quality ad-
ministrative systems that are critical to their combination, gathering and capacity. Secondary metabolites have essential defense
and flagging jobs, and they add to the general quality of creating and aging natural products. Particularly, light conditions and tem-
perature are exhibited to have an unmistakable job on the organization of phenolic compounds. The present survey centers around
the examinations on components related with the guideline of key secondary metabolites, mostly phenolic compounds, in different
plants. are a helpful cluster of normal items as well as an essential piece of plant defense framework against pathogenic assaults and
environmental stresses. With astounding biological exercises, plant SMs are progressively utilized as drug fixings and nourishment
added substances for remedial, fragrant and culinary purposes. Different hereditary, ontogenic, morphogenetic and environmental
components can impact the biosynthesis and aggregation of SMs. As indicated by the writing reports, for instance, SMs gathering is
unequivocally reliant on an assortment of environmental factors, for example, light, temperature, soil water, soil richness and salti-
ness, and for most plants, an adjustment in an individual factor may modify the substance of SMs regardless of whether different
elements stay steady. Here, we survey with accentuation how every one of single elements to influence the collection of plant sec-
ondary metabolites, and lead a relative examination of applicable normal items in the stressed and unstressed plants. Hopefully, this
narrative survey will diagram a general picture of environmental elements in charge of change in plant SMs, give a handy method to
get reliable quality and high amount of bioactive compounds in vegetation, and present a few proposals for future innovative work.
Keywords: Terms; Medicinal Plants; Organic Compounds; Secondary Metabolite; Biosynthesis
Citation: Mohi Uddin. “Environmental Factors on Secondary Metabolism of Medicinal Plants”. Acta Scientific Pharmaceutical Sciences 3.8 (2019): 34-46.
Environmental Factors on Secondary Metabolism of Medicinal Plants
35
Biosynthesis
The pathways of biosynthesis are in charge of the event of both
essential and secondary metabolites showed in figure 1 biosyn-
thetic reactions are vitality devouring, filled by the vitality dis-
charged by glycolysis of sugars and through the citrus extract cycle.
Oxidation of glucose, unsaturated fats and amino acids results in
ATP development, which is a high-vitality atom shaped by catabo-
lism of essential compounds. ATP is reused in fuel anabolic reac-
tions including middle of the road atoms on the pathways. Though,
catabolism includes oxidation of beginning atoms, biosynthesis
or anabolism includes decrease response. Henceforth, the need of
lessening operator or hydrogen contributor, which is generally the
NADP. These impetuses are known as coenzymes and the most gen-
erally happening is CoA comprised of ADP and pantetheine phos-
Figure 1: Cell Metabolic Cycle and Production of Secondary me-
phate. The most well-known pathways taken for biosynthesis are
tabolites. Plants are sessile organisms and, in order to defend them-
performed through the pentose for glycosides, polysaccharides;
selves against exogenous (a)biotic constraints, they synthesize an
shikimic acid for phenols, tannins, sweet-smelling alkaloids; acetic
array of secondary metabolites which have important physiological
acid derivation malonate for phenols and alkaloids and mevalonic
and ecological effects. Plant secondary metabolites can be classified
acid for terpenes, steroids and alkaloids. As appeared in the figure
into four major classes: terpenoids, phenolic compounds, alkaloids
1, the plan plots how metabolites from the procedure of photo-
and sulphur-containing compounds. These phytochemicals can be
synthesis, glycolysis and Krebs cycle are tapped off from vitality
antimicrobial, act as attractants/repellents, or as deterrents against
producing procedure to give biosynthetic intermediates. By a long
herbivores. The synthesis of such a rich variety of phytochemicals
shot, the essential structure squares utilized in the biosynthesis of
is also observed in undifferentiated plant cells under laboratory
secondary metabolites are gotten from Acetyl-CoA, shikimic acid,
conditions and can be further induced with elicitors or by feeding
mevalonic acid and 1-deoxylulose 5-phosphate [1-7] (Figure 2).
precursors (Source: Guerriero G, Berni R, Muñoz-Sanchez JA, et al.
Production of Plant Secondary Metabolites: Examples, Tips and
Expression of secondary metabolites Suggestions for Biotechnologists. Genes (Basel). 2018;9(6):309.
The nearness of or nonattendance of certain secondary metabo- Published 2018 Jun 20. doi:10.3390/genes9060309).
lites in restorative plants are affected by an assortment of compo-
nents, which incorporate atmosphere/season, edaphic conditions
or the relationship of different plants and other living creatures
number of eggs and the hatchlings that rise up out of these eggs
[8,9]. Another factor that affected the creation of secondary me-
at that point feed on leaves of the plants, some of the time oblit-
tabolites in plants are the entomb connection among plants and
erating the plants through and through by over bolstering. Over
the bug greenery. It is currently commonly acknowledged that the
the span of advancement, the plants started to integrate certain
vegetation and the creepy crawly greenery in a tropical biological
dangerous substance so a decent level of the bolstering hatchlings
system have been co-developing and co-adjusting. A considerable
could be murdered [12-14]. The bug then again started to create
lot of the therapeutic plants are cross-pollinated and they need
obstruction with the goal that a significant number of the hatch-
the assistance of pollinators. In an open territory the breeze could
lings could endure. The plants then again balanced. It orchestrat-
do the capacity, yet in a canopied woods a considerable lot of the
ing an ever increasing number of poisonous compounds. This was
bushes and herbs becoming under the enormous trees can't get
something like the adoration and loathe connection among plants
wind to fertilize. These plants are in this manner intensely relying
and the creepy crawlies, which over the span of a great many long
on the creepy crawlies or even the feathered creatures to fertil-
stretches of advancements have brought about the combination of
ize them. To pull in the creepy crawlies or fowls the plants create
incalculable concoction compounds, for the most part the second-
charming smell (basic oils) and give nectar and dust as sustenance
ary metabolites in plants just as in bugs [15,16]. The changeabil-
to these pollinators. Numerous blooms contain nectar or dust,
ity in living life forms is in reality the protection for survival. The
which are the ordinary nourishment of numerous creepy crawlies
transformative root of cross rearing was for sure a nature's gadget
and feathered creatures [10,11]. The creepy crawlies like honey
for reshuffling of qualities so new variations could be delivered.
bees and butterflies visit many flowers, and take nectar or dust
Thus, the abiotic conditions likewise applied certain impact in the
or both. Amid this procedure they likewise convey dust on their
plants and the plants reacted by creating different synthetic com-
body part, which at that point help in pollinating while at the same
pounds [17]. In outrageous dry spell conditions the desert applies
time visiting different plants. Numerous blooms have basically
a sort of stress on the plants and the plants develop by combining
advanced blossom parts to influence such fertilizations by bugs.
synthetics that would assist them with protecting from stress actu-
These creepy crawlies likewise duplicate on plants. They lay a huge
ated by the desert conditions. An incredible case for this is the plant
Citation: Mohi Uddin. “Environmental Factors on Secondary Metabolism of Medicinal Plants”. Acta Scientific Pharmaceutical Sciences 3.8 (2019): 34-46.
Environmental Factors on Secondary Metabolism of Medicinal Plants
36
this plant developing in a warm damp tropical backwoods locale. and biosynthesis of SMs. Plant development and profitability is ad-
It has no desert like conditions and hence there is no doubt of any versely influenced by temperature boundaries, saltiness, and dry
dry season incited stress. A similar plant when developing in des- spell stress. Plant SMs are compounds that have a fundamental im-
ert needs to stand up to dry season prompted stress and the plant pact in the association of plants with abiotic stresses [25]. What's
incorporates the stress beating synthetic substances. There are nu- more, plant development and advancement are additionally to a
merous comparative cases that show that specific explicit climatic great extent intervened by the endogenous dimensions of these
conditions and edaphic circumstances are critical in the creation SMs. A wide scope of SMs are delivered from essential metabolites,
of restoratively attractive therapeutic compounds. Sandalwood is for example, amino acids, lipids, and sugars in higher plants. Spe-
another traditional model. The particular fragrance of sandalwood cific hues, tastes, and scents of plants are related with SMs. Plant
is because of the nearness of certain fundamental oil synthetic con- SMs additionally fill in as fundamental wellsprings of modernly
coctions, generally monoterpenes and sesquiterpenes. The genera- vital synthetic concoctions, flavors, sustenance added substances,
tion of the particular fragrance synthetic compounds is completely and pharmaceuticals [26]. Plants amass such compounds in light
communicated just in those sandalwood trees that develop in cer- of various flagging particles. SM generation is affected by different
tain woods areas of Karnataka. The sandalwood developing in dif- environmental stresses. Environmental elements decide the blend
ferent places in India or somewhere else on the planet don't have a and resulting amassing of SM. Adjustment in any one factor triggers
irritations in the biosynthesis of plant SMs [27].
Citation: Mohi Uddin. “Environmental Factors on Secondary Metabolism of Medicinal Plants”. Acta Scientific Pharmaceutical Sciences 3.8 (2019): 34-46.
Environmental Factors on Secondary Metabolism of Medicinal Plants
37
Citation: Mohi Uddin. “Environmental Factors on Secondary Metabolism of Medicinal Plants”. Acta Scientific Pharmaceutical Sciences 3.8 (2019): 34-46.
Environmental Factors on Secondary Metabolism of Medicinal Plants
38
Citation: Mohi Uddin. “Environmental Factors on Secondary Metabolism of Medicinal Plants”. Acta Scientific Pharmaceutical Sciences 3.8 (2019): 34-46.
Environmental Factors on Secondary Metabolism of Medicinal Plants
39
Metabolite Class Metabolite Name Structural Image Environment Factor Concentration Change Plant Species
Alkaloids Camptothecin 27% Full sunlight Increase C. acuminate
Table 2: Light intensity changes on the content of various plant SMs [42-45].
Citation: Mohi Uddin. “Environmental Factors on Secondary Metabolism of Medicinal Plants”. Acta Scientific Pharmaceutical Sciences 3.8 (2019): 34-46.
Environmental Factors on Secondary Metabolism of Medicinal Plants
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Citation: Mohi Uddin. “Environmental Factors on Secondary Metabolism of Medicinal Plants”. Acta Scientific Pharmaceutical Sciences 3.8 (2019): 34-46.
Environmental Factors on Secondary Metabolism of Medicinal Plants
41
Metabolite Class Metabolite Name Structural Image Environment Factor Concentration Change Plant Species
Phenols Ferulic acid Increase red light Decrease L. sativa
Table 3: Light quality change on the content of various plant SMs [46-51].
(10-HCPT), an indole alkaloid detached from a Chinese tree, Camp- Pelargonidin chloride is an anthocyanidin chloride that has pelar-
totheca sharpen, hinders the movement of topoisomerase I and has gonidin as the cationic partner. It has a job as a phytoestrogen and
a wide range of anticancer action in vitro and in vivo. In any case, its a plant metabolite. It contains a pelargonidin.
utilization has been constrained because of its water-insolubility
and danger with i.v. organization. Isoprene is combined through Reaction of Plant SMs to Soil and Water
the 2-C-methylerythritol-5-phosphate (MEP) pathway that ad- Water stress is a standout amongst the most critical environ-
ditionally delivers abscisic acid (ABA). Increments in foliar free mental stresses that can direct the morphological development and
ABA focus amid dry spell incite stomatal conclusion and may like- advancement of plants, and modify their biochemical properties.
wise adjust ethylene biosynthesis. This first report on α-farnesene Serious water shortage has been considered to decrease the plants
union in Y. lipolytica establishes a framework for future research development, however a few examinations have exhibited that wa-
on creation of sesquitepenes in Y. lipolytica and other nearest yeast ter stress might be conceivable to build the measure of SMs in a
species and will conceivably contribute in its modern generation. wide assortment of plant species [59,60] (Figure 8).
Citation: Mohi Uddin. “Environmental Factors on Secondary Metabolism of Medicinal Plants”. Acta Scientific Pharmaceutical Sciences 3.8 (2019): 34-46.
Environmental Factors on Secondary Metabolism of Medicinal Plants
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Metabolite Class Metabolite Name Structural Image Environment Factor Concentration Change Plant Species
Alkaloids Morphine Low temperature Decrease P. somniferum
Salidroside is segregated from Rhodiola rosea and is one of the gestion, antiarrhythmic impact, and improvement of angiogenesis.
fundamental dynamic segments in Rhodiola species. Rhodiola ro- Tanshinone IIA (Tan-IIA) is gotten from the dried underlying foun-
sea has for quite some time been utilized as a restorative plant and dations of Salvia miltiorrhiza Bunge, a customary Chinese medica-
has been accounted for to have different pharmacological proper- tion. Despite the fact that Salvia miltiorrhiza has been connected
ties, including antifatigue and against stress movement, anticancer, for a long time, the poisonous quality of the mono-constituent of
cancer prevention agent and safe upgrading and animating sexual Salvia miltiorrhiza, tanshinone IIA, is still understudied. Sub-atom-
action, hostile to aggravation, improvement of glucose and lipid di- ic proof found with cryptotanshinone for treatment and avoidance
Citation: Mohi Uddin. “Environmental Factors on Secondary Metabolism of Medicinal Plants”. Acta Scientific Pharmaceutical Sciences 3.8 (2019): 34-46.
Environmental Factors on Secondary Metabolism of Medicinal Plants
43
Metabolite Class Metabolite Name Structural Image Environment Factor Concentration Change Plant Species
Phenols Salidroside Soil moisture of 55– Increase R. sachalinen-
75% sis
Table 5: Soil water change on the content of various plant SMs [61-64].
of human malignancy. Blend of the perfect solute glycine betaine stances of these metabolites like there is recuperation of the items
presents an extensive level of osmotic stress resilience to Bacillus will be simple and plant societies are especially helpful in the event
subtilis. Ongoing investigation uncovers that abietic acid can be of plants which are troublesome or costly and determination of
created as an injury recuperating specialist. cell lines for high return of secondary metabolites will be simple.
Numerous different precedents could be given plant metabolic de-
Epilogue signing as this exploration zone is growing effectively. Metabolic
building is likely an expansive advance forward yet playing on the
SMs are the helpful regular items that are blended through sec-
qualities won't take care of the considerable number of issues that
ondary digestion in the plants. The generation of some secondary
have kept the improvement of business achievement in the field of
metabolites is connected to the enlistment of morphological sepa-
plant secondary metabolites. Furthermore, Advances in plant cell
ration and it gives the idea that as the phones experience morpho-
societies could give new intends to the savvy, business creation of
logical separation and development amid plant development. It is
even uncommon or colorful plants, their cells, and the synthetic
seen that in-Vitro creation of secondary metabolites is a lot higher
substances that they will deliver. Learning of the biosynthetic path-
from separated tissues when contrasted with non-separated or
ways of wanted compounds in plants just as of societies is regu-
less – separated tissues. There are bunches of favorable circum-
Citation: Mohi Uddin. “Environmental Factors on Secondary Metabolism of Medicinal Plants”. Acta Scientific Pharmaceutical Sciences 3.8 (2019): 34-46.
Environmental Factors on Secondary Metabolism of Medicinal Plants
44
larly still simple, and procedures are thus expected to create data 6. Aly Farag El Sheikha. “Medicinal Plants: Ethno-Uses to Bio-
dependent on a cell and atomic dimension. In view of the complex technology Era”. Affiliation: Department of Biology, McMas-
and not entirely comprehended nature of plant cells in-vitro soci- ter University, 1280 Main St. West, Hamilton, ON, L8S 4K1,
eties, case-by-contextual analyses have been utilized to clarify the Canada
Citation: Mohi Uddin. “Environmental Factors on Secondary Metabolism of Medicinal Plants”. Acta Scientific Pharmaceutical Sciences 3.8 (2019): 34-46.
Environmental Factors on Secondary Metabolism of Medicinal Plants
45
10. Claire Brittain., et al. “Pollination and Plant Resources Change 24. Fumihiko Sato. “Plant Secondary Metabolism”.
the Nutritional Quality of Almonds for Human Health”. PLoS
One 9.2 (2014): e90082. 25. Zhang B. “MicroRNA: a new target for improving plant toler-
ance to abiotic stress”. Journal of Experimental Botany 66.7
11. Koppert Biological System Why do pollinators visit flowers?. (2015): 1749-1761.
12. Ferris Jabr Farming a Toxin to Keep Crops Healthy Scientific 26. Singh R., et al. “Microbial metabolites in nutrition, healthcare
American The Sciences (2013). and agriculture”. 3 Biotech. 7.1 (2017): 15.
13. Ryan A Blaedow. “Forest Health Handbook North Carolina 27. Ashraf MA., et al. “Environmental Stress and Secondary
Forest Service 3rd Edition Publisher”. (2011). Metabolites in Plants: An Overview”. Plant Metabolites and
Regulation Under Environmental Stress Chapter 8 (2018):
14. Crop Scouting Manual Field Crop Integrated Pest Manage- 153-167.
ment Program - University of Wisconsin-Extension - Coop-
erative Extension Service (2010). 28. Sulmon C., et al. “Abiotic stressors and stress responses: What
commonalities appear between species across biological or-
15. Douglas J Futuymaa and Anurag A Agrawalb. “Macroevolu- ganization levels?”. Environmental Pollution 202 (2015): 66-
tion and the biological diversity of plants and herbivores”. 77.
Proceedings of the National Academy of Sciences of the United
States of America 106.43 (2009): 18054-18061. 29. Rejeb IB., et al. “Plant Responses to Simultaneous Biotic and
Abiotic Stress: Molecular Mechanisms”. Plants (Basel) 3.4
16. Marcia O Mello and Marcio C. “Silva-Filho Plant-insect in- (2014): 458-475.
teractions: an evolutionary arms race between two distinct
defense mechanisms”. Brazil Journal of Plant Physiology 41.2 30. Saddique M., et al. “Differential Responses of Plants to Biotic
(2002). Stress and the Role of Metabolites”. Plant Metabolites and
Regulation under Environmental Stress (2018): 69-87.
17. “Plant Evolutionary Biology Copyright Publisher Name
Springer, Dordrecht Information Springer Science+ Business 31. Cragg GM and Newman DJ. “Natural products: a continuing
Media B.V. (1988). source of novel drug leads”. Biochimica et Biophysica Acta
1830.6 (2013): 3670-3695.
18. Neeraj Jain and Rajani S Nadgauda. “Commiphora wightii
(Arnott) Bhandari—A Natural Source of Guggulsterone: Fac- 32. Hussain MS., et al. “Current approaches toward production of
ing a High Risk of Extinction in Its Natural Habitat”. American secondary plant metabolites”. Journal of Pharmacy and Bioal-
Journal of Plant Sciences 4.6A (2013): 57-68. lied Sciences 4.1 (2012): 10-20.
19. Nakuleshwar Dut Jasuja., et al. “Review on Bioactive Com- 33. Breitling R., et al. “Metabolomics for secondary metabolite
pounds and Medicinal Uses of Commiphora mukul”. A Review research”. Metabolites 3.4 (2013): 1076-1083.
on Bioactive Compounds and Medicinal Uses of Commiphora
mukul”. Journal of Plant Sciences 7 (2012): 113-137. 34. Eibl R., et al. “Plant cell culture technology in the cosmetics
and food industries: current state and future trends”. Applied
20. Medicinal Plants Utilisation and Conservation 2nd Revised Microbiology and Biotechnology 102.20 (2018): 8661-8675.
and Enlarged Edition Editor Prof. Pravin Chandra Trivedi
Publisher: Aavishkar Publishers, Distributors Jaipur 302 003 35. Wilson SA and Roberts SC. “Recent advances towards de-
(Raj) India. velopment and commercialization of plant cell culture pro-
cesses for the synthesis of biomolecules”. Plant Biotechnology
21. Schäfer H and Wink M. “Medicinally important secondary Journal 10.3 (2012): 249-268.
metabolites in recombinant microorganisms or plants: prog-
ress in alkaloid biosynthesis”. Biotechnology Journal 4.12 36. Yang L., et al. “Response of Plant Secondary Metabolites to
(2009):1684-1703. Environmental Factors”. Molecules 23.4 (2018): 762.
22. Michael Wink “Chapter 11 Importance of plant secondary 37. dos Santos MD., et al. “Effects of caffeoylquinic acid deriva-
metabolites for protection against insects and microbial in- tives and C-flavonoid from Lychnophora ericoides on in vitro
fections”. Advances in Phytomedicine 3 (2007): 251-268. inflammatory mediator production”. Natural Product Com-
munications 5.5 (2010): 733-740.
23. Michael Wink “Plant breeding: importance of plant second-
ary metabolites for protection against pathogens and her- 38. Skrovankova S., et al. “Bioactive Compounds and Antioxidant
bivores”. Theoretical and Applied Genetics 75.2 (1988): 225- Activity in Different Types of Berries”. International Journal of
233. Molecular Sciences 16.10 (2015): 24673-24706.
Citation: Mohi Uddin. “Environmental Factors on Secondary Metabolism of Medicinal Plants”. Acta Scientific Pharmaceutical Sciences 3.8 (2019): 34-46.
Environmental Factors on Secondary Metabolism of Medicinal Plants
46
39. Del Rio D., et al. “Bioavailability of coffee chlorogenic acids 53. Janas KM., et al. “Constitutive elevated accumulation of phen-
and green tea flavan-3-ols”. Nutrient 2.8 (2010): 820-833. ylpropanoids in soybean roots at low temperature”. Plant Sci-
ence 163.2 (2002): 369-373.
40. Monteiro M., et al. “Chlorogenic acid compounds from coffee
are differentially absorbed and metabolized in humans”. The 54. Irrera N., et al. “Dietary Management of Skin Health: The Role
Journal of Nutrition 137.10 (2007): 2196-2201. of Genistein”. Nutrients 9.6 (2017): 622.
41. National Center for Biotechnology Information. PubChem 55. Poschner S., et al. “The Impacts of Genistein and Daidzein on
Compound Database; CID=135, https://pubchem.ncbi.nlm. Estrogen Conjugations in Human Breast Cancer Cells: A Tar-
nih.gov/compound/135 (accessed Jan. 16, 2019). geted Metabolomics Approach”. Frontiers in Pharmacology 8
(2017): 699.
42. Hashimoto T and Yamada Y. “Alkaloid biogenesis: Molecular
aspects”. Annual Review of Plant Biology 45 (1994): 257-285. 56. Ping YH., et al. “Anticancer effects of low-dose 10-hydroxyc-
amptothecin in human colon cancer”. Oncology Reports 15.5
43. Vincent RM., et al. “Sustained harvest of camptothecin from (2006):1273-1279.
the leaves of Camptotheca acuminate”. Journal of Natural
Products 60.6 (1997): 618-619. 57. Yang X., et al. “Heterologous production of α-farnesene in
metabolically engineered strains of Yarrowia lipolytica”. Bio-
44. Gottschalk KW Shade. “leaf growth and crown development resource Technology 216 (2016): 1040-1048.
of quercus rubra, quercus velutina, prunus serotina and acer
rubrum seedlings”. Tree Physiology 14.7-9 (1994): 735-749. 58. National Center for Biotechnology Information. PubChem
Compound Database; CID=67249, https://pubchem.ncbi.
45. Liu Z., et al. “Camptothecin production in Camptotheca acu- nlm.nih.gov/compound/67249 (accessed Jan. 16, 2019).
minata seedlings in response to shading and flooding”. Cana-
dian Journal of Botany 75 (1997): 368-373. 59. Zobayed SMA., et al. “Phytochemical and physiological chang-
es in the leaves of St. John’s wort plants under a water stress
46. Kim OT., et al. “Characterization of the Asiatic Acid Glucos- condition”. Environmental and Experimental Botany 59.2
yltransferase, UGT73AH1, Involved in Asiaticoside Biosyn- (2007): 109-116.
thesis in Centella asiatica (L.) Urban”. International Journal of
Molecular Sciences 18.12 (2017): 2630. 60. Zhu Z., et al. “Impact of fertilization on drought response in
the medicinal herb Bupleurum chinense DC: Growth and
47. Liu LF., et al. “Mechanism of action of camptothecin”. Annals saikosaponin production”. Industrial Crops and Products
of the New York Academy of Sciences 922 (2000): 1-10. 29.2-3 (2009): 629-633.
48. Srinivasan M., et al. “Ferulic Acid: therapeutic potential 61. Zhang BC., et al. “Salidroside decreases atherosclerotic
through its antioxidant property”. Journal of Clinical Bio- plaque formation in low-density lipoprotein receptor-defi-
chemistry and Nutrition 40.2 (2007): 92-100. cient mice”. Evidence-Based Complementary and Alternative
Medicine (2012): 607508.
49. Benyammi R., et al. “Screening and kinetic studies of cath-
aranthine and ajmalicine accumulation and their correlation 62. Wang T., et al. “Evaluation of Tanshinone IIA Developmental
with growth biomass in Catharanthus roseus hairy roots”. Toxicity in Zebrafish Embryos”. Molecules 22.4 (2017). E660.
Pharmaceutical Biology 54.10 (2016): 2033-2043.
63. Chen W., et al. “Molecular evidence of cryptotanshinone for
50. Ishikawa H., et al. “Direct coupling of catharanthine and treatment and prevention of human cancer”. Anti-Cancer
vindoline to provide vinblastine: total synthesis of (+)- and Agents in Medicinal Chemistry 13.7 (2013): 979-987.
ent-(-)-vinblastine”. Journal of the American Chemical Society
130.2 (2008): 420-421. 64. Park JY., et al. “Abietic acid isolated from pine resin (Resina
Pini) enhances angiogenesis in HUVECs and accelerates cuta-
51. Azevedo MI., et al. “The antioxidant effects of the flavonoids neous wound healing in mice”. Journal of Ethnopharmacology
rutin and quercetin inhibit oxaliplatin-induced chronic pain- 203 (2017): 279-287.
ful peripheral neuropathy”. Molecular Pain 9 (2013): 53.
52. Bernáth J and Tétényi P. “The Effect of environmental fac- Volume 3 Issue 8 August 2019
tors on growth. Development and alkaloid production of © All rights are reserved by Mohi Uddin.
Poppy (Papaver somniferum L.): I. Responses to day-length
and light intensity”. Biochemie und Physiologie der Pflanzen
174.5-6 (1979): 468-478.
Citation: Mohi Uddin. “Environmental Factors on Secondary Metabolism of Medicinal Plants”. Acta Scientific Pharmaceutical Sciences 3.8 (2019): 34-46.