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| Schematic representation of a neuron illustrating the major cellular sites and cell organelles that are influenced by endogenous farnesol-like sesquiterpenoids, as highlighted by the red asterisks. This list is not exhaustive (e.g., the figure does not list the mitochondria which are known targets of farnesol/JH). The functional relation between farnesol/FLS and the Ca 2+ -homeostasis system with its numerous actors, explains why there are so many target sites. This figure is combinatorial: the asterisks represent data from different experimental models. The basic idea underlying this figure is also valid for other cell types, in particular for those with an active RER-Golgi system. This figure, borrowed from Google pictures, specifically focuses on axonal transport. (A) Large peptide molecules (pre-propeptides) are converted into smaller peptides (propeptides) in the rough endoplasmic reticulum. The propeptides and enzymes are packaged into vesicles that are transported to the Golgi apparatus, modified, and packaged into vesicles. The vesicles get attached to microtubules and are carried to the terminals by fast axonal transport. The propeptides are cleaved into smaller peptidergic transmitters in the axon's terminal. The peptide neurotransmitters are released into the synaptic cleft by exocytosis. Surplus membrane elements in the terminal are carried back to the cell body by retrograde transport. The retrieved vesicular membrane is degraded or recycled. (B) A model showing how kinesin (a microtubule-associated ATPase) can move an organelle along a microtubule. Copyright information: This figure is listed in Google Images, without specific information on the authors, only general information. From: What-when-how; In Depth Tutorials and Information; Histology of the Nervous System (The Neuron) Part 1, The Neuron figure 5-2. With thanks to the anonymous author(s). For lack of information, Open Access is assumed.

| Schematic representation of a neuron illustrating the major cellular sites and cell organelles that are influenced by endogenous farnesol-like sesquiterpenoids, as highlighted by the red asterisks. This list is not exhaustive (e.g., the figure does not list the mitochondria which are known targets of farnesol/JH). The functional relation between farnesol/FLS and the Ca 2+ -homeostasis system with its numerous actors, explains why there are so many target sites. This figure is combinatorial: the asterisks represent data from different experimental models. The basic idea underlying this figure is also valid for other cell types, in particular for those with an active RER-Golgi system. This figure, borrowed from Google pictures, specifically focuses on axonal transport. (A) Large peptide molecules (pre-propeptides) are converted into smaller peptides (propeptides) in the rough endoplasmic reticulum. The propeptides and enzymes are packaged into vesicles that are transported to the Golgi apparatus, modified, and packaged into vesicles. The vesicles get attached to microtubules and are carried to the terminals by fast axonal transport. The propeptides are cleaved into smaller peptidergic transmitters in the axon's terminal. The peptide neurotransmitters are released into the synaptic cleft by exocytosis. Surplus membrane elements in the terminal are carried back to the cell body by retrograde transport. The retrieved vesicular membrane is degraded or recycled. (B) A model showing how kinesin (a microtubule-associated ATPase) can move an organelle along a microtubule. Copyright information: This figure is listed in Google Images, without specific information on the authors, only general information. From: What-when-how; In Depth Tutorials and Information; Histology of the Nervous System (The Neuron) Part 1, The Neuron figure 5-2. With thanks to the anonymous author(s). For lack of information, Open Access is assumed.

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Farnesol, the sesquiterpenoid precursor of the six presently known insect juvenile hormones (JHs) was for the first time chemically identified in 1961, not in JH synthesizing glands or whole body extracts, but in excrements of the mealworm Tenebrio molitor. This finding was thought to be irrelevant and remained unexplored. In 1970, it was reported...

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... It acts as a precursor of the juvenile hormones of holometabolous insects and its absence in the larval stage induces metamorphosis. 52 Knowing the MoA of farnesol would allow for an improved effectiveness in the formulations, because if its activity is the result of a hormonal effect, its application should be performed during the nymphal stages of aphids. This could explain why it is more effective when applied to smaller colonies (with a greater number of nymphs). ...
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BACKGROUND Myzus persicae (Hemiptera: Aphididae) is considered one of most important agricultural pests in the world. It is one of the main pests in protected pepper crops under glasshouse conditions in Southeastern Spain, but its control is limited as a consequence of the few available authorized insecticides and their incompatibility with the natural enemies. Some essential oils and pure compounds such as anise (Pimpinella anisum) or farnesol are repellent and/or toxic to aphids. Their use as a botanical insecticides can be an alternative for aphid control in pepper. RESULTS The effect of farnesol was evaluated against M. persicae in a new bioassay developed to test the contact effect (aqueous formulation of the products) on aphids in laboratory conditions. Aniseed essential oil, geraniol and (Z)‐jasmone at 0.6% causes an aphid mortality of >50%; and farnesol was the most effective (93.67% mortality). Farnesol nanoemulsions between 0.2% and 0.6% were formulated with an IKA‐Labor Pilot dispersing machine (7940 rpm for 10 min) using Tween 80 as a surfactant. These formulations were tested on field experiments (glasshouse conditions) on pepper crops for 2 years. Foliar applications of farnesol at a concentration of 0.4% in field conditions causes a high reduction in aphid populations, with efficacies of ≈70–80% with respect to the control, similar to or even higher than the efficacy of the reference pyrethrin insecticide. CONCLUSION Farnesol showed a great aphicidal effect against M. persicae. The use of this molecule in integrated pest management programs combined with natural enemies is a good option for future control of M. persicae. © 2022 Society of Chemical Industry.
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The extensive literature dealing with the Golgi system emphasizes its role in protein secretion and modification, usually without specifying from which evolutionary ancient cell physiological necessity such secretion originated. Neither does it specify which functional requirements the secreted proteins must meet. From a reinterpretation of some classical and recent data gained mainly, but not exclusively, from (insect) endocrinology, the view emerged that the likely primordial function of the rough endoplasmic reticulum (RER)–Golgi complex in all eukaryotes was not the secretion of any type of protein but the removal of toxic excess Ca²⁺ from the cytoplasm. Such activity requires the concurrent secretion of large amounts of Ca²⁺-carrying/transporting proteins acting as a micro-conveyor belt system inside the RER–Golgi. Thus, (fitness increasing) protein secretion is subordinate to Ca²⁺ removal. Milk with its high content of protein and Ca²⁺ (60–90 mM vs. 100 nM in unstimulated mammary gland cells) is an extreme example. The sarco(endo)plasmatic reticulum Ca²⁺-ATPases (SERCAs) and SPCA1a Ca²⁺/Mn²⁺ transport ATPases are major players in Ca²⁺ removal through the Golgi. Both are blocked by the sesquiterpenoid thapsigargin. This strengthens the hypothesis (2014) that endogenous farnesol-like sesquiterpenoids (FLSs) may act as the long sought for but still unidentified agonist(s) for Ca²⁺-pumps in both the ER and Golgi. A second putative function also emerges. The fusion of both the incoming and outgoing transport vesicles, respectively, at the cis- and trans- side of Golgi stacks, with the membrane system requiring high flexibility and fast self-closing of the involved membranes. These properties may—possibly partially—be controlled by endogenous hydrophobic membrane “fluidizers” for which FLSs are prime candidates. A recent reexamination of unexplained classical data suggests that they are likely synthesized by the Golgi itself. This game-changing hypothesis is endorsed by several arguments and data, some of which date from 1964, that the insect corpus allatum (CA), which is the major production site of farnesol-esters, has active Golgi systems. Thus, in addition to secreting FLS, in particular juvenile hormone(s), it also secretes a protein(s) or peptide(s) with thus far unknown function. This paper suggests answers to various open questions in cell physiology and general endocrinology.