6-chloro-6-deoxyglucose and trichlorosucrose

Comparative neuropathological studies of 1,6-dichloro-1, 6-dideoxy-beta-D-fructofuranosyl-4-chloro-4-deoxy-alpha-D-galactopyra noside (sucralose), an equimolar mixture of 1,6-dichloro-1, 6-dideoxyfructose (1,6-DCF) and 4-chloro-4-deoxygalactose (4-CG), the hydrolysis products of sucralose, and 6-chloro-6-deoxyglucose (6-CG) were conducted in male and female mice and male marmoset monkeys, focusing on morphological changes in the central nervous system. 6-Chloro-6-deoxyglucose, previously reported to produce neurotoxic effects, served as the positive control and was administered by gavage at a daily dose of 500mg/kg. Sucralose and the sucralose hydrolysis products (sucralose-HP) were similarly administered to mice and marmosets at doses of up to 1000mg/kg for 21 and 28 days, respectively. No changes were detected in the central nervous system by light or electron microscopy in either of the species that received sucralose or its hydrolysis products. 6-Chloro-6-deoxyglucose, in contrast, induced symmetrical lesions in the deep nuclei of the cerebellum, brain stem and spinal cord with definitive neurological signs of CNS involvement.

Topics: Administration, Oral; Animals; Callithrix; Central Nervous System; Cerebellar Nuclei; Deoxy Sugars; Deoxyglucose; Female; Fructose; Fucose; Histocytochemistry; Hydrolysis; Male; Medulla Oblongata; Mice; Microglia; Microscopy, Electron; Posture; Random Allocation; Reflex; Sciatic Nerve; Spinal Cord; Sucrose; Sweetening Agents

The structural basis of the sweet taste of D-galactose, D-glucose, D-mannose, sucrose, and some of their chlorinated derivatives has been derived from an interpretation of their F.t.-i.r. spectra. AH-B glucophores are proposed in the light of the observed OH vibrations, and an explanation of the differences in sweetness of the monosaccharides is proposed. The hydrophobic character of the CH2Cl, "gamma" centre in the tripartite template does not seem to play the same role in monosaccharides and 4,1',6'-trichloro-4,1',6'-trideoxy-galacto-sucrose. The enhancement of sweetness in the disaccharide derivative is due to the enhanced hydrophobicity of the CH2Cl groups as well as to specific interactions with water. A sharp i.r. absorption characteristic of free hydroxyl is found in the spectra of most of the very sweet polyhydroxy compounds.

Topics: Deoxyglucose; Fucose; Galactose; Glucose; Humans; Solutions; Spectrophotometry, Infrared; Structure-Activity Relationship; Sucrose; Taste