Mode of action of the ecdysone agonist tebufenozide (RH-5992), and an exclusion mechanism to explain resistance to it

Arthur Retnakaran; Ivan Gelbic; Meenakshi Sundaram; William Tomkins; Tim Ladd; Mark Primavera; Qili Feng; Basil Arif; Reddy Palli; Peter Krell

doi:10.1002/ps.377

Mode of action of the ecdysone agonist tebufenozide (RH-5992), and an exclusion mechanism to explain resistance to it

Pest Management Science ◽

10.1002/ps.377 ◽

2001 ◽

Vol 57 (10) ◽

pp. 951-957 ◽

Cited By ~ 37

Author(s):

Arthur Retnakaran ◽

Ivan Gelbic ◽

Meenakshi Sundaram ◽

William Tomkins ◽

Tim Ladd ◽

...

Keyword(s):

Mode Of Action ◽

Exclusion Mechanism ◽

Ecdysone Agonist

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Induction of autotomy in the American bird grasshopperSchistocerca americana (Drury) by the ecdysone agonist RH-5849 and investigation of its mode of action

Cellular and Molecular Life Sciences ◽

10.1007/bf01922414 ◽

1996 ◽

Vol 52 (1) ◽

pp. 42-50 ◽

Cited By ~ 10

Author(s):

F. Ortego ◽

W. S. Bowers

Keyword(s):

Mode Of Action ◽

Ecdysone Agonist

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Effects of 5-5'-Diphenyl-2-thiohydantoin (DPTH) and Thyroxine on the Ultrastructure and Chemical Composition of Rat Liver

Proceedings, annual meeting, Electron Microscopy Society of America ◽

10.1017/s0424820100066917 ◽

1971 ◽

Vol 29 ◽

pp. 570-571

Author(s):

E. A. Elfont ◽

R. B. Tobin ◽

D. G. Colton ◽

M. A. Mehlman

Keyword(s):

Chemical Composition ◽

Rat Liver ◽

Future Study ◽

Mode Of Action ◽

Liver Mitochondria ◽

Rat Liver Mitochondria ◽

Effective Inhibitor ◽

Biochemical Effects ◽

Glycerophosphate Dehydrogenase ◽

Stimulation Of

Summary5,-5'-diphenyl-2-thiohydantoin (DPTH) is an effective inhibitor of thyroxine (T4) stimulation of α-glycerophosphate dehydrogenase in rat liver mitochondria. Because this finding indicated a possible tool for future study of the mode of action of thyroxine, the ultrastructural and biochemical effects of DPTH and/or thyroxine on rat liver mere investigated.Rats were fed either standard or DPTH (0.06%) diet for 30 days before T4 (250 ug/kg/day) was injected. Injection of T4 occurred daily for 10 days prior to sacrifice. After removal of the liver and kidneys, part of the tissue was frozen at -50°C for later biocheailcal analyses, while the rest was prefixed in buffered 3.5X glutaraldehyde (390 mOs) and post-fixed in buffered 1Z OsO4 (376 mOs). Tissues were embedded in Araldlte 502 and the sections examined in a Zeiss EM 9S.Hepatocytes from hyperthyroid rats (Fig. 2) demonstrated enlarged and more numerous mitochondria than those of controls (Fig. 1). Glycogen was almost totally absent from the cytoplasm of the T4-treated rats.

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