Startseite Evaluation of efficacy of Aloe vera (L.) Burm. f. gel solution in methylcellulose-induced ocular hypertension in New Zealand white rabbits
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Evaluation of efficacy of Aloe vera (L.) Burm. f. gel solution in methylcellulose-induced ocular hypertension in New Zealand white rabbits

  • Jhanvi J. Vaghela ORCID logo , Manish J. Barvaliya , Sugnesh J. Parmar und Chandrabhanu R. Tripathi EMAIL logo
Veröffentlicht/Copyright: 10. November 2020

Abstract

Objectives

The present study aimed to evaluate the efficacy of Aloe vera in the methylcellulose-induced ocular hypertension model.

Methods

Fifty-six rabbits were randomly divided into seven groups. Intraocular pressure (IOP) was raised by anterior chamber injection of 2% methylcellulose in all the groups except the normal control group. Disease control animals were treated with sterile water and active control with topical 0.5% timolol 12 hourly; 6 and 12% A. vera gel topical solutions 8 hourly were given in group IV and V, respectively; 6 and 12% A. vera gel solutions along with timolol were given in group VI and VII animals, respectively. Mean IOP values and percentage of reduction in IOP were compared at 15 min, 30 min, 1 h, 2 h, 4 h, 8 h, 12 h, 24 h, 36 h, and 48 h.

Results

A. vera gel solutions (6 and 12%) showed a significant reduction in mean IOP from 4 to 2 h time points, respectively, whereas, A. vera gel solutions (6 and 12%) + timolol showed significant less mean IOP from a 30 min time point as compared with disease control. A. vera gel solutions (6 and 12%) showed 8.6 and 10.4% more reduction in IOP, respectively (66.8 ± 4.9% and 68.6 ± 5.4% vs. 58.2 ± 2.3%; p > 0.05), whereas 6 and 12% A. vera gel solutions along with timolol showed 14.5 and 16.2% more reduction in IOP, respectively (72.7 ± 4.7% and 74.4 ± 4.1% vs. 58.2 ± 2.3%; p < 0.05), than disease control group at 48 h.

Conclusions

Six and twelve percent A. vera gel solutions reduced the IOP effectively. Concurrent treatment with 12% A. vera gel and timolol produced the maximum reduction in IOP.


Corresponding author: Dr. Chandrabhanu R. Tripathi, M.D. Pharmacology, Former Dean and Professor Pharmacology, Government Medical College and Sir Takhtsinhji General Hospital, Bhavnagar 364001, Gujarat, India, Phone: +91 98259 51678, E-mail:

Funding source: Department of Pharmacology, Government Medical College

Acknowledgments

The authors are thankful to Dr. Tejas K. Patel, Associate Professor, Pharmacology, All India Institute of Science, Gorakhpur, Uttar Pradesh, for critical review of the manuscript.

  1. Research funding: Department of Pharmacology, Government Medical College, Bhavnagar-364001, (Gujarat), India.

  2. Author contributions: All authors have accepted responsibility for the entire content of this manuscript and approved its submission.

  3. Competing interests: Authors state no conflict of interest.

  4. Ethical approval: All the experiments were performed after a prior approval of the Institutional Animal Ethics Committee (IAEC), Government Medical College, Bhavnagar, Gujarat, India (Approval no.-51/2016, Approval date-25/06/2016). New Zealand white rabbits were procured from the Central Animal House of Government Medical College, Bhavnagar (Registration number is 577/GO/Re/S/02/CPCSEA dated 9th August 2016). All the experiments were performed as per guidelines given by the Committee for the Purpose of Control and Supervision on Experiments on Animals (CPCSEA), Ministry of Forest and Environment, Government of India.

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Received: 2019-06-13
Accepted: 2020-04-09
Published Online: 2020-11-10

© 2020 Walter de Gruyter GmbH, Berlin/Boston

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