ABSTRACT
The insects are a class of invertebrates within the arthropod phylum that have a chitinous
exoskeleton. The leaf eating insects obtain their nutrients and growth promoting biocompounds from
the variable or specific flora available for them. The plants on earth are the richest source of
metabolites including juvenile hormone analogues for leaf eating insects like silkworm, Bombyx mori
(L). Some of plant origin metabolites are acting as insects juvenoids for insect lives. They serve to
take pause in the progression of metamorphosis through arresting some of the biochemical reactions
including chitin synthesis or accelerating progression through other biochemical pathways in the larval
body of insects. The ten microliters of various concentrations of acetone solution of Fernasol Methyl
Ether (FME) and each selected monoterpene compounds (Myrcene; Camphene; Cymene; Limonene
and Eucalyptol ) were used for topical application to individual larval instars of silkworm, Bombyx
mori (L) (Race: PM x CSR2) at 48 hours after the fourth moult. The integument chitin of untreated
control larvae; acetone treated control; FME treated larvae and monoterpene treated larvae was
estimated at 120 hours after the fourth moult. Topical application of selected concentrations of acetone
solutions of selected monoterpenes to fifth instar larvae of silkworm, Bombyx mori (L) (Race: PM x
CSR2) was found reflected into the reduction in the deposition of chitin in the larval body wall. The
reduction in body wall chitin was found ranging from zero to hundred percent. The plot of
concentrations of acetone solutions of FME and monoterepene compounds and percent reduction in
the body wall chitin was found exhibiting a characteristic Sigmoid form of displacement, which
herewith titled as “Punyamayee Baramati Dose Response Curve”. Since the effects of juvenoids
involve the inhibition of metamorphosis through reduction in chitin deposition, it is possible to express
the concentration (dose) applied in terms of ID50 value. The ID50 value of juvenoid contents of FME
and selected monoterpene compounds can be defined as the specific unit (microgram), which enable to
chitin to deposit fifty percent less in the body wall of larvae (In comparison with untreated control).
Accordingly, the ID50 value calculated from the “Punyamayee Baramati Dose Response Curves” for
FME was found measured 0.08 mg/ml. The ID50 values for monoterpene compounds: Myrcene;
Camphene; Cymene; Limonene and Eucalyptol were found measured: 0.116; 0.122; 0.164; 0.172 and
0.208 mg/ml respectively. Acetone soluble juvenoid content of terpene compounds may be utilized
efficiently for the fortified development of fifth instars of silkworm, Bombyx mori (L) and thereby, the
cocoon quality. Sigmoid (S-form) “Baramati Dose Response Curve” may help for quantitative
estimation of juvenoid contents of various terpene compounds and terpenoids.
References
[1] Ajami, A. M. and Riddiford, L. M. (1973). Comparative metabolism of the cecropia
juvenile hormone. J. Insect Physiol. 19: 635-646.
[2] Baishya, R. L. and Hazarika, L. R. (1996). Effect of methoprene and diflubenzuron on
water, lipid, protein and chitin of Dicladispa armigera (Coleoptera: Chrysomelidae).
Entomon, 21 91(1): 7-11.
[3] Calvez, B., Hirn, M. and Reggi, M. (1976). Progress of development programme during
the last larval instar of Bombyx mori (L). Relationship with food intake, ecdyosteroids
and juvenile hormone. Journal of Insect Physiology, 24(4): 233-239.
[4] Gopakumar B., Ambika, B. and Prabhu, V. K. K. (1977). Juvenmimetic activity in some
south Indian plants and their probable cause of this activity in Morus alba (L). Entomon,2: 259-261.
[5] Grenier and Grenier (1983). Fenoxycarb, a fairlynew growth regulator: a review of its
effects on insects. Ann. App. Biol. 122: 369-403.
[6] Jadhav G. and Kallapur V. L. (1989). Contribution of tissue protein to the cocoon shell
in the fifth instar silk worm, Bombyx mori (L).
[7] Kamimura M. and Kiguchi M. (1980). Effect of juvenile hormone analogue on fifth
stadium larvae of silk worm, Bombyx mori (L) (Lepidoptera: Bombycidae). Appl.
Entomol. Zool. 33(2): 333-338.
[8] Khyade, V. B., Patil, S. B., Khyade, S. V. and Bhawane G. P. (2002). Influence of
acetone maceratives of Vitis vinifera on the larval parameters of silk worm, Bombyx
mori (L). Indian Journal of Comparative Animal Physiology, 20: 14-18.
[9] Khyade V. B., Patil, S. B., Khyade, S. V. and Bhawane, G. P. (2003). Influence of
acetone maceratives of Vitis vinifera on the economic parameters of silk worm,
Bombyx mori (L). Indian Journal of Comparative Animal Physiology. 21: 28-32.
[10] Khyade V. B. (2004). Influence of juvenoids on silk worm, Bombyx mori (L). Ph.D.
Thesis, Shivaji University, Kolhapur, India.
[11] Khyade, V. B. and Ganga V. Mhamane (2005). Vividh Vanaspati Arkancha Tuti
Reshim Kitak Sangopanasathi Upyojana. Krishi Vdnyan. 4, 18-22.
[12] Khyade, V. B.; Poonam B. Patil; M. Jaybhay; Rasika R. Gaikwad; Ghantaloo, U. S.;
Vandana D. Shinde; Kavita H. Nimbalkar and Sarwade, J. P. (2007). Use of digoxin for
improvement of economic parameters in silk worm, Bombyx mori (L). Bioinfrmatics
(Zoological Society of India).
[13] Krishnaswami, S., Narasimhana, M. N., Suryanarayana, S. K. and Kumaraj, S. (1978).
Sericulture Manual – ll: Silk worm Rearing. F A O , United Nation’s Rome: 131.
[14] Mamatha, D. N., Nagalakshmma, K. and Rajeshwara Rao, M. (1999). Impact of
selected Juvenile Hormone Mimics on the organic constituents of silk worm, Bombyx
mori (L).
[15] Norman, T. J. and Baily (1955). Statistical Methods.
[16] Omana Joy and Shyamala, M. B. (1983). Non-spinning syndrome in silk worm:
Occurrence and Pathology. Research paper presented for National Seminar on silk
research and development, Banglore, India.
[17] Prabhu, V. K. K., John, M. and Ambika, B. (1973). Juvenile hormone activity in some
south Indian plants. Current Science, 42: 72-726.
[18] Ratnasen (1988). How does juvenile hormone cause more silk yield. Indian Silk: 21-22.
[19] Riddiford, L. M. (1985). Hormone action at cellular level. In: Comprehensive Insect
Physiology, Biochemistry and Pharmacology. G. A. Kerkut and L. I. Gilbert (Eds.). 8:
37-64. (Pergamon press, Oxford).
[20] Riddiford, L. M. (1994). Cellular and molecular actions of Juvenile hormone: General
consideration and premetamorphic actions. J. Adv. Insect Physiology. 24: 213-214.
[21] Sehnal F. and Rambold, H. (1985). Brain stimulation and juvenile hormone production
in insect larvae. Experentia. 44: 684-685.
[22] Slama, K. (1969). Plant as source material with insect hormone activity. Ent. Exp. Appl.
12: 721-728.
[23] Slama, K. (1971). Insect juvenile hormone analogues. Ann. Rev. Biochem. 40: 1079-1102.
[24] Slama, K., Romanuk, M. and Sorm, F. (1974). Insect hormones and Bioanalogues.
Springer Verlag, Wein and New York.
[25] Slama, K. (1985). Pharmacology of Insect Juvenile Hormones. In: Comprehensive
Insect Physiology, Biochemistry and Pharmacology. (Eds. G. A. Kerkut and L. I.
Gilbert). Vol. 11: 357-394. Pergamon Press, Oxford, New York.
[26] Slama, K. (1979). Insect Hormones and anti-hormones in plants. Herbivores, their
interaction with secondary plant metabolites. (Eds. G. A . Rosenthal and D. H. Janzen;
Academic Press, New York ): 683-700.
[27] Williams, C. M. (1956). The Juvenile Hormone of Insects. Nature. 178: 212-213.
[28] Zaoral, M. and Slama, K. (1970). Peptides with juvenile hormone activity. Science. 170: 92-93.
[29] Jagtap, Sharad G. (2007). Effect of plant juvenoids on consumption and utilization of
mulberry leaves by silkworm, Bombyx mori (L). M. Phil. Dissertation, Alagappa
University, Karaikudi – 630003 (India ).
[30] Vitthalrao B. Khyade and Karel Slama (2015). Screening of acetone solution of FME
and Selected Monoterpene Compounds for Juvenile Hormone Activity Through
Changes in pattern of Chitin Deposition in the Integument of Fifth instar larvae of
silkworm, Bombyx mori (L) (PM x CSR2). IJBRITISH, 2(3) (2015) 68-90.
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