Effects of co-administration of Unani pharmacopoeia formulations Qurs Tabasheer Sartani and Arq Hara Bhara with CAT-I antitubercular drugs in rats

Author:

Ahmed Noor Zaheer1,Agibothu Kupparam Hemanth Kumar2,Akbar Seema3,Hissar Syed2,Anwar Noman1,Thiruvengadam Kannan2,Anjum Nighat4,Khan Asim Ali4,Dar Showkat3,Natarajan Saravanan2ORCID

Affiliation:

1. Regional Research Institute of Unani Medicine (RRIUM) , Chennai , Tamil Nadu , India

2. ICMR-National Institute for Research in Tuberculosis (NIRT) , Chennai , Tamil Nadu , India

3. Regional Research Institute of Unani Medicine (RRIUM) , Srinagar , Jammu & Kashmir , India

4. Central Council for Research in Unani Medicine, Ministry of AYUSH , Govt. of India , New Delhi , India

Abstract

Abstract Objectives Tuberculosis continues to be a major public health problem globally, despite incredible advancements in healthcare system. In Unani system of medicine, Qurs Tabasheer Sarthani (QTS) and Arq Hara Bhara (AHB) have been traditionally used for tuberculosis like conditions. The study was aimed to investigate the effects of co-administration of QTS and AHB with category I first line antitubercular drugs (CAT-I) on the indices of liver and kidney function in rats. Methods QTS and AHB were prepared individually and mixed to achieve final compound Unani pharmacopoeia formulation (UPF). The human equivalent doses for rats were calculated and administered with and without CAT-I. The effects of the formulations on serum indices of kidney and liver function, hematological markers and plasma CAT-I drug levels were estimated at 14th, 60th & 180th days of treatment. Results The administration of UPF, CAT-I and UPF + CAT-I altered the levels of aspartate transaminase (AST), alanine transaminase (ALT), alkaline phosphatase (ALP) and gamma glutamyltransferase (GGT) and haematological markers. These alterations were within permissible range and randomly distributed among groups during various time points. Administration of CAT-I alone resulted in moderate histopathological changes which were completely abrogated in CAT-I + UPF co-administered animals. The co-administration of UPF with CAT-I improved the plasma peak rifampicin (RIF) levels, without altering the liver and kidney functions. Conclusions The co-administration of UPF with ATT improved liver and kidney functions and increased the plasma levels of RIF. These beneficial findings provide a scope to evaluate the pharmacokinetic studies in humans.

Publisher

Walter de Gruyter GmbH

Subject

Complementary and alternative medicine

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