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Chemical Compound Review

Hexacosanol     hexacosan-1-ol

Synonyms: n-Hexacosanol, Hexacosan-1-ol, CERYL ALCOHOL, CPD-7871, NSC-4058, ...
 
 
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Disease relevance of n-Hexacosanol

  • Treatment with N-hexacosanol did not alter the diabetic status of the animals, i.e., body weight, serum glucose, and serum insulin levels, but significantly restored the thickness of intestine wall and ameliorated diabetes-induced hypercontractility of the rat ileum in a dose-dependent manner [1].
  • Diabetes induced bladder smooth muscle hypertrophy, which tended to be ameliorated by treatment with n-hexacosanol in a dose-dependent manner [2].
 

High impact information on n-Hexacosanol

 

Biological context of n-Hexacosanol

 

Anatomical context of n-Hexacosanol

  • The maintenance of AChE-positive neurons was particularly striking in the vertical limb of the diagonal band of Broca, where 83% of the neurons survived after two weeks of n-hexacosanol treatment compared to 51% in the non-treated animals [8].
  • It is concluded that n-hexacosanol at 10(-9) M and 10(-7) M exerts an inhibitory effect on insulin secretion stimulated by glucose in vivo and in vitro in the rat, suggesting a direct effect on islets of Langerhans [6].
  • Peripherally administered n-hexacosanol, a long-chain fatty alcohol, strongly attenuated the degeneration of cholinergic neurons in the medial septum and the vertical limb of the diagonal band of Broca following transection of their dorsal projection to the hippocampus by unilateral fimbria-fornix aspiration [8].
  • Our data indicate that N-hexacosanol could reverse diabetes-induced hypercontractility in the rat trachea [9].
 

Associations of n-Hexacosanol with other chemical compounds

  • In this study, we investigated the effects of cyclohexenonic long-chain fatty alcohol (N-hexacosanol) on streptozotocin-diabetic hypercontractility in the rat ileum longitudinal muscles [1].
 

Analytical, diagnostic and therapeutic context of n-Hexacosanol

References

  1. N-hexacosanol reverses diabetic induced muscarinic hypercontractility of ileum in the rat. Shinbori, C., Saito, M., Kinoshita, Y., Satoh, I., Kono, T., Hanada, T., Nanba, E., Adachi, K., Suzuki, H., Yamada, M., Satoh, K. Eur. J. Pharmacol. (2006) [Pubmed]
  2. Preventive effects of cyclohexenonic long-chain fatty alcohol on diabetic cystopathy in the rat. Suzuki, H., Saito, M., Kinoshita, Y., Satoh, I., Kono, T., ShinBori, C., Anastasios, S., Yamada, M., Satoh, K. Can. J. Physiol. Pharmacol. (2006) [Pubmed]
  3. Enhancement of mouse sciatic nerve regeneration by the long chain fatty alcohol, N-Hexacosanol. Azzouz,, M., Kenel, P.F., Warter J-M, n.u.l.l., Poindron, P., Borg, J. Exp. Neurol. (1996) [Pubmed]
  4. The neurotrophic factor, n-hexacosanol, reduces the neuronal damage induced by the neurotoxin, kainic acid. Borg, J. J. Neurosci. Res. (1991) [Pubmed]
  5. Ability of cyclohexenonic long-chain Fatty alcohol to reverse diabetes-induced cystopathy in the rat. Saito, M., Kinoshita, Y., Satoh, I., Shinbori, C., Suzuki, H., Yamada, M., Watanabe, T., Satoh, K. Eur. Urol. (2007) [Pubmed]
  6. Effect of n-hexacosanol on insulin secretion in the rat. Damgé, C., Hillaire-Buys, D., Koenig, M., Gross, R., Hoeltzel, A., Chapal, J., Balboni, G., Borg, J., Ribes, G. Eur. J. Pharmacol. (1995) [Pubmed]
  7. Studies on the immunological effects of fatty alcohols--I. Effects of n-hexacosanol on murine macrophages in culture. Moosbrugger, I., Bischoff, P., Beck, J.P., Luu, B., Borg, J. Int. J. Immunopharmacol. (1992) [Pubmed]
  8. Peripheral administration of a long-chain fatty alcohol promotes septal cholinergic neurons survival after fimbria-fornix transection. Borg, J., Kesslak, P.J., Cotman, C.W. Brain Res. (1990) [Pubmed]
  9. Treatment with cyclohexenonic long-chain Fatty alcohol reverses diabetes-induced tracheal dysfunction in the rat. Hanada, T., Saito, M., Kanzaki, S. Pharmacology (2006) [Pubmed]
  10. Cuticular wax deposition in growing barley (Hordeum vulgare) leaves commences in relation to the point of emergence of epidermal cells from the sheaths of older leaves. Richardson, A., Franke, R., Kerstiens, G., Jarvis, M., Schreiber, L., Fricke, W. Planta (2005) [Pubmed]
 
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