In insects, JH (formerly neotenin) refers to a group of hormones, which ensure growth of the larva, while preventing metamorphosis. Because of their rigid exoskeleton, insects grow in their development by successively shedding their exoskeleton (a process known as molting).
Juvenile hormones are secreted by a pair of endocrine glands behind the brain called the corpora allata. JHs are also important for the production of eggs in female insects.
Most insect species contain only juvenile growth hormone (JH) III.[5] To date JH 0, JH I, and JH II have been identified only in the Lepidoptera (butterflies and moths). The form JHB3 (JH III bisepoxide) appears to be the most important JH in the Diptera, or flies.[6] Certain species of crustaceans have been shown to produce and secrete methyl farnesoate, which is juvenile hormone III lacking the epoxide group.[7] Methyl farnesoate is believed to play a role similar to that of JH in crustaceans.
Being a sesquiterpenoid, JH chemical structure differs significantly from the structure of other animal hormones. Some JH analogs have been found in conifers.[8]
^Riddiford, L. M. (1994). "Cellular and molecular actions of juvenile hormone I. General considerations and premetamorphic actions". Advances in Insect Physiology. 24: 213–274. doi:10.1016/S0065-2806(08)60084-3. ISBN9780120242245.
^Watt, G. R.; Davey, K. G. (1996). "Cellular and Molecular Actions of Juvenile Hormone. II. Roles of Juvenile Hormone in Adult Insects". Advances in Insect Physiology. 26: 1–155. doi:10.1016/S0065-2806(08)60030-2. ISBN9780120242269.
^Nijhout, H. F. (1994). Insect Hormones. Princeton: Princeton University Press.
^Röller, H.; Dahm, K.H.; Sweeley, C.C.; Trost, B.M. (1967). "The Structure of the Juvenile Hormone". Angewandte Chemie International Edition. 6 (2): 179–180. doi:10.1002/anie.196701792.
^Rogers, I. H.; J. F. Manville; T. Sahota (April 1974). "Juvenile Hormone Analogs in Conifers. II. Isolation, Identification, and Biological Activity of cis-4-[1′(R)-5′-Dimethyl-3′-oxohexyl]-cyclohexane-1-carboxylic Acid and (+)-4(R)-[1′(R)-5′-Dimethyl-3′-oxohexyl]-1-cyclohexene-1-carboxylic Acid from Douglas-fir Wood". Canadian Journal of Chemistry. 52 (7): 1192–1199. doi:10.1139/v74-187.