TY - JOUR
T1 - Marihuana-derived material
T2 - Biochemical studies of the ocular responses
AU - Green, Keith
AU - Cheeks, Kenneth
AU - Mittag, Tom
AU - Riley, Michael V.
AU - Symonds, Christopher M.
AU - Deutsch, Howard M.
AU - Hodges, Linda C.
AU - Zalkow, Leon H.
N1 - Funding Information:
ACKNOWLEDGEMENT Supported in part by PHS Research Grants EY04572 (KG), EY02619 (TM), EY00541 (MVR), and EY03352 (LHZ) from the National Eye Institute, and in part
Funding Information:
by National Glaucoma Research, a program of the American Health Assistance Foundation (KG), and in part by a departmental award to the Department of Ophthalmology, Medical College of Georgia from Research to Prevent Blindness, Inc. We thank Mrs. Sylvia Catravas for excellent secretarial assistance and Professor K. Folkers, Institute for Biomedical Research, University of Texas, Austin, Texas, for generously supplying the substance P antagonist.
PY - 1985
Y1 - 1985
N2 - Some biochemical factors of the iris-ciliary body of the rabbit have been examined for effects induced by water-soluble marihuana-derived material (MDM). Adenylate cyclase activity and sensitivity to βadrenergic agonists were unchanged, as measured 4 hours after MDM administration in vivo. Magnesium-dependent and anion-sensitive, but not sodium-potassium, ATPase activities were inhibited 6 hours after MDM administration in vivo, although they were unaffected by in vitro incubation. Topical administration of a potent substance P antagonist had no effect on the time course or magnitude of intravenous MDM-induced ocular effects in rabbit. Intravenously administered sugars antagonized the effects of MDM on intraocular pressure. A variety of drugs which display a range of biochemical effects varying from beta-adrenergic receptor agonism, to alteration of glycoprotein residues were employed. None of the agents employed, ranging from cAMP modifiers to protein synthesis blockers, had any effect on the MDM-induced response. It is apparent that the mechanism underlying the ocular hypotensive effect of MDM does not reside in mediation through adenylate cyclase, ATPase or substance P, but rather through a mechanism mediated by terminal sugar moieties on the molecule. The data suggest that modification of the surface membrane glycoprotein residues on the ciliary epithelium can induce marked alterations in aqueous humor flow rate.
AB - Some biochemical factors of the iris-ciliary body of the rabbit have been examined for effects induced by water-soluble marihuana-derived material (MDM). Adenylate cyclase activity and sensitivity to βadrenergic agonists were unchanged, as measured 4 hours after MDM administration in vivo. Magnesium-dependent and anion-sensitive, but not sodium-potassium, ATPase activities were inhibited 6 hours after MDM administration in vivo, although they were unaffected by in vitro incubation. Topical administration of a potent substance P antagonist had no effect on the time course or magnitude of intravenous MDM-induced ocular effects in rabbit. Intravenously administered sugars antagonized the effects of MDM on intraocular pressure. A variety of drugs which display a range of biochemical effects varying from beta-adrenergic receptor agonism, to alteration of glycoprotein residues were employed. None of the agents employed, ranging from cAMP modifiers to protein synthesis blockers, had any effect on the MDM-induced response. It is apparent that the mechanism underlying the ocular hypotensive effect of MDM does not reside in mediation through adenylate cyclase, ATPase or substance P, but rather through a mechanism mediated by terminal sugar moieties on the molecule. The data suggest that modification of the surface membrane glycoprotein residues on the ciliary epithelium can induce marked alterations in aqueous humor flow rate.
UR - https://www.scopus.com/pages/publications/0021868277
U2 - 10.3109/02713688508999996
DO - 10.3109/02713688508999996
M3 - Article
C2 - 3160544
AN - SCOPUS:0021868277
SN - 0271-3683
VL - 4
SP - 631
EP - 640
JO - Current Eye Research
JF - Current Eye Research
IS - 5
ER -